The Personalized Lifestyle Medicine Institute Announces the 11th Annual Thought Leaders Consortium

SEATTLE, WA, Aug 22, 2023 – (ACN Newswire) – The Personalized Lifestyle Medicine Institute (PLMI) is excited to bring together researchers, clinicians, industry leaders, and anyone interested in Functional Medicine for its 11th Annual Thought Leaders Consortium: Next Generation Clinical Management of Chronic Neuroimmune Disorders this October in Seattle, WA.


Personalized Lifestyle Medicine Institute – 11th Annual Thought Leaders Consortium


The two-day event, located at the Seattle Marriott Waterfront, features leading innovators in the application of next-generation approaches for managing complex chronic neuroimmune disorders and will focus on recent discoveries and how to translate this information into clinical practice.

The program will explore the root causes of illness, the complexity of genetic and epigenetic influences, and the power of lifestyle, diet, and environmental and social factors that can impact therapeutic outcomes, with an emphasis on skill development, faculty interaction, and dynamic attendee participation.

With more than 35 countries represented, this immersive educational event is a realization of PLMI's mission to bring together researchers, clinicians, industry leaders, media leaders, and other stakeholders to focus on new models of healthcare delivery, advancements in medical nutrition therapy, and exciting emerging science.

Beginning on October 20, the first session focuses on advances in the management of neuroimmune disorders, with speakers including Jeffrey Bland, Ph.D., who has spent more than four decades focused on the improvement of human health and is known worldwide as the founder of the Functional Medicine movement. His pioneering work created PLMI as well as the Institute for Functional Medicine (IFM). Other topics will include the unique features of specific plant foods in managing neuroimmune disorders and genomic testing and what it says about the risk of neuroimmune disorders.

Three more engaging sessions will be covered during the event with topics including neuroimmune assessment and intervention, advances in personalizing neuroimmune interventions, and advances in repairing broken brain-behavior connections. Attendees will hear from internationally recognized experts such as Dr. Terry Wahls, Aristo Vojdani, PhD, MD, Bridget Briggs, MD, Deanna Minich, Ph.D., CNS, Dale Bredesen, MD, and more. For a full list of speakers and their topics, see the event agenda here.

The last session will also include a discussion period among faculty and attendees and end with closing comments from Dr. Bland.

PLMI looks forward to exploring these approaches to managing chronic conditions with the consortium's attendees. Space is limited at the event, and those wishing to attend can register here.

About PLMI

The mission of the Personalized Lifestyle Medicine Institute is to bring together researchers, clinicians, industry leaders, media leaders, and other stakeholders to focus on new models of healthcare delivery, advancements in medical nutrition therapy, and exciting emerging science. Our vision encompasses building a community around dynamic collaborations, compelling dialogues, evidence-based information and resources, and immersive educational events. Since 1991, hundreds of thousands of healthcare practitioners have participated in PLMI programs, and this collective knowledge has positively impacted the lives of patients all over the world.

Contact Information
Nicole Fox
Media Management
info@plminstitute.org
(206) 201-3794

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Welcome to the World of Holistic Beauty – The Epitome of Health and Beauty with LAC MASQUELIER’s(R) French Pine Bark Extract

SINGAPORE, Aug 21, 2023 – (ACN Newswire) – What if the key to timeless beauty lies not in cosmetics or skincare products, but in our inner health? Gone are the days when beauty was merely skin deep, defined by cosmetics and outward enhancements. The buzzwords – Holistic Beauty – have been in the rage recently, where the concept of Holistic Beauty recognises that our physical appearance is a reflection of our overall health.




Introducing the unsung hero of beauty and health: Antioxidants. These remarkable allies offer a more effective and long-term solution for women seeking radiance and vitality. Antioxidants, found in foods or supplements like French Pine Bark Extract, can help protect the skin from oxidative stress caused by free radicals. This protection may assist in maintaining skin elasticity, reducing the appearance of fine lines and wrinkles, and promoting a radiant complexion.

At LAC, we redefine the concept of beauty, promoting a deeper meaning behind achieving radiant skin. We encourage individuals to prioritise overall wellness, recognising that a nourished body and balanced mindset contribute to long-term beauty and well-being.

Offering a holistic approach to beauty that goes beyond superficial enhancements, LAC MASQUELIER's(R) French Pine Bark Extract antioxidant work from within, helping to counteract oxidative stress and free radicals that can contribute to premature ageing and other skin-related concerns.

Loaded with oligomeric proanthocyanidins (OPCs), a potent antioxidant, LAC MASQUELIER's(R) French Pine Bark Extract reduces the amount of free radicals in the body, allowing the body to combat pathogens and infections effectively.

About LAC Global

Headquartered in Singapore, LAC Global is one of Asia's largest speciality retailers in nutritional supplements, vitamins, minerals, herbal, and other speciality supplements in Anti-ageing and Beauty, Immunity, Weight Management, Sports Nutrition, and Energy.

The Company owns the LAC brand, short for Leader in Antioxidative Control(TM), a leading health and wellness supplement brand with a global presence. Since its founding, LAC has embarked on a pioneering journey to develop scientifically based formulas, harnessing the best of eastern wisdom and western technology to fight free radicals, combat ageing brought forth by oxidative stress, and support you daily in looking, feeling, and functioning at your best. Having established a global presence since 1997, LAC's reach includes Singapore, Malaysia, Taiwan, Philippines, China, Japan, Vietnam, Myanmar, USA, Central & South Americas, and the Middle East. Currently, there are more than 220 LAC branded stores in Singapore, Malaysia, Philippines and Taiwan ROC. LAC stringently sources ingredients from around the globe, such as USA, Japan, France, Australia, New Zealand and Switzerland to ensure utmost quality, and works only with the most specialised partners in developing and manufacturing health solutions.

Its other brands include Xndo Food For Health. LAC Global is dedicated to ensuring consumers stay well, and live life to the fullest.

Website: LAC.sg
Instagram: @LACGlobalSingapore
Facebook: @LACGlobalSingapore

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

WholisticResearch Reveals the Best Nootropics of 2023

LONDON, Aug 18, 2023 – (ACN Newswire) – WholisticResearch, a leading authority in the realm of cognitive enhancement research, has recently unveiled its list of the top nootropic supplements for 2023. Following rigorous testing and comprehensive analysis, the organization has identified the most effective cognitive enhancers available on the market today. Authored by Jacob Kovacs, the head researcher at WholisticResearch, the article delves into the top nootropics that may enhance cognitive abilities.


Best Nootropics


Understanding Nootropics

Nootropics, often referred to as "brain boosters," have gained significant attention for their potential to boost focus, productivity, memory, and mood. As the article states, "Nootropics are a new class of brain enhancers that may increase focus and productivity, enhance memory, and improve mood." With a plethora of options available on the market, the article serves as a guide to understanding which nootropics are truly effective.

Jacob Kovacs emphasizes the importance of making informed choices. He notes, "There are several cognitive enhancers that are being researched for their potential to increase mental performance, cognitive function, and mental health." The article further elaborates on how these nootropics function, their pros and cons, and what makes them stand out.

Methodology

WholisticResearch employed a meticulous testing and review process to determine the top-quality nootropics. This process encompassed factors such as effectiveness, ingredients, brand reputation, transparency, production method, user feedback, price, and value.

A Comprehensive Approach

WholisticResearch's article is not just a list but a comprehensive guide. It details the mechanism of action of nootropics, stating, "Nootropics are substances that may improve cognitive function, memory, and focus. They may also help to increase intelligence and creativity." The article also addresses frequently asked questions about nootropics, ensuring readers are well-informed.

The Challenges of Cognitive Enhancement

Cognitive enhancement is not a straightforward process. The brain is a complex environment for compounds, and intricate cognitive enhancement strategies are required. WholisticResearch acknowledges that new compounds are increasingly adopting complicated strategies. They emphasize that hands-on research is crucial to determining the correct product and its manufacturing process.

About WholisticResearch

Founded in 2019, WholisticResearch has been at the forefront of cognitive enhancement research. Their primary focus is on the latest nootropics and peptides that can potentially improve cognitive function. The organization also reviews the most recent research on vitamins and supplements that may boost cognition. WholisticResearch continues to be a beacon of information and research in the realm of cognitive enhancement, driven by a team of dedicated professionals.

Contact Information
Jacob Kovacs
Author
jacob@wholisticresearch.com

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Asensus Surgical Continues to Spearhead Innovations and Growth in Surgical Robotics

NEW YORK, Aug 17, 2023 – (ACN Newswire) – PCG Digital — Driving towards its goal of continued global growth in the surgical robotics sector, Asensus Surgical (NYSE American: ASXC) provided a positive update on both recent accomplishments and the company's projected outlook for the coming year. Asensus' trajectory shows strong promise and interest, with marked advancements in the adoption of its state-of-the-art products and a clear vision for future innovations.



Q2 in Review:

– Progress across Key Areas: The company reported meaningful progress across its key areas, including the broader utilization of the Intelligent Surgical Unit(TM) (ISU(TM)), the advancement of their clinical body of evidence, and the continued optimization of their flagship product, Senhance(R) Surgical System.

– Robust Worldwide Growth: A 27% year-over-year growth was observed in the second quarter, with more than 1,000 Senhance procedures performed globally. This consistent growth rate of around 10% sequentially underscores the firm's commitment to expansion and stability.

– Global Reach: Asensus Surgical continues to make international inroads. Notably, the initiation of the Senhance program at Fukuoka Tokushukai Hospital in Kasuga City, Japan, and the successful establishment of an exclusive Senhance program within the pediatric surgery department of a leading U.S. hospital indicates its expanding global footprint and trajectory.

– Pediatric Space Advancements: Pediatric surgeons are drawn to the Senhance system's specialized features, smaller instruments, and real-world data demonstrating safety and effectiveness in the wake of Asensus obtaining FDA clearance in March 2023.

– Clinical Registry Expansion: The TRUST(TM) clinical registry, which collects both intraoperative and postoperative follow-up data, has expanded to include data from over 2,500 patients. This data supports quality clinical publications and aids in the company's market development strategy.

– Active Participation in Industry Events: Asensus Surgical participated in several key industry events, including the Society of Robotic Surgery Annual Meeting in Australia and the joint meeting of IPEG and ESPES, to generate excitement and showcase the capabilities of Senhance, LUNA, and the ISU.

Financial Overview:

Asensus reported revenue of $1.1 million for Q2 2023, a slight increase from $1 million in Q2 2022. This includes lease revenue, instruments, and accessories as well as services. Although there was a reported net loss of $20.7 million for Q2 2023, the company's strong cash position, bolstered by a recent offering that generated approximately $10 million, extends the company's cash runway through the second quarter of 2024.

Strategic and Surgical Precision

– LUNA Surgical System: The upcoming LUNA Surgical System is a significant development. By the end of 2023, the company aims to complete full system integration and testing for LUNA. Regulatory filings are anticipated in late 2024, with hopes of FDA clearance by mid-2025. This would pave the way for a commercial launch in the second half of 2025.

– Economic Flexibility: With LUNA, Asensus is considering a subscription-based model for hospitals, offering an innovative approach to ensure broader adoption without increasing procedure costs.

– Expansion of ISU and Senhance: 2023 will also see Asensus entering into an agreement with a strategic graphics hardware provider and ramping up pilot manufacturing for the future ISU. Furthermore, a total of 10 to 12 new Senhance programs are expected to be initiated throughout the year.

A Closer Look:

Anthony Fernando, President and CEO at Asensus, attributes ongoing growth to two key factors: 1) More surgeons within the same hospital adopting the system and 2) Additional installations coming up to speed.

Fernando has previously stated that from a pipeline point of view, Asensus feels very bullish and that it can deliver on its commitment of 10 to 12 systems. Fernando further commented on the timing of the additional systems that the decision cycle is a long one because hospitals are doing the diligence and trying to get as much consensus internally as they can with surgeons so they can make the program successful.

Fernando added that pediatrics is "somewhat of an underserved space" and that the value of smaller instruments, haptic feedback, and innovative digital capabilities is becoming more and more attractive to pediatric surgeons, particularly in the United States.

Finally, the team is making excellent progress on the LUNA R&D front. They continue to receive positive feedback from surgeons who are looking forward to utilizing both 3- and 5-millimeter instruments as well as eye-tracking features and independent arms: "They can see the improvements, and that's what's driving a high level of interest," Fernando added.

Asensus Surgical's recent achievements and future plans suggest a company that is not only growing but also driving significant innovations in digital surgery. With their commitment to delivering better outcomes for patients and continuous advancements, the company's trajectory of sustained growth and leadership in its domain is drawing surgeons, patients, and investors alike.

Disclaimer

This communication was produced by PCG Digital Holdings, LLC, an affiliate of PCG Advisory Inc., (together "PCG"). PCG is not a registered or licensed broker-dealer nor investment adviser. No information contained in this communication constitutes an offer to sell, a solicitation of an offer to buy, or a recommendation of any security. PCG may be compensated by respective clients for publicizing information relating to its client's securities. See www.pcgadvisory.com/disclosures.

PCG Digital
info@pcgadvisory.com
646-863-6341

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

OrbusNeich FY2023 Interim Net Profit Triples to US$25.2 Million, Total Revenue Increases by 18.2% to US$81.4 Million

HONG KONG, Aug 17, 2023 – (ACN Newswire) – OrbusNeich Medical Group Holdings Limited ("OrbusNeich" or the "Group"; stock code: 6929), a major global medical device manufacturer specializing in interventional devices for percutaneous coronary intervention (PCI) and percutaneous transluminal angioplasty (PTA) procedures, today announced its interim results for the six months ended 30 June 2023, reporting growth in both revenue and net profit.

Results Highlights:
— Revenue grew 18.2% to US$81.4 million, while revenue (excluding FX impact) growth rate reached 23.5%
— Net profit rose 213.3% year-on-year to US$25.2 million with net profit margin of 30.9%; while adjusted profit (non-HKFRS measure) (1) increased by 105.6% to approximately US$25.4 million
— Total sales volume increased by 20.8% to approximately 725,000 units
— The Group had over 210 granted patents and published patent applications worldwide
— The Group obtained CE Marks for the Scoreflex TRIO Balloon Dilatation Catheter and EZ Guide Guiding Extension Catheter and renewed the CE Mark for the Sapphire PTCA Family under the MDR
— Expansion of the Group's Shenzhen production base will bring the total annual production capacity to 1.8 million units of balloons and 60,000 units of stent products
— The Group's Hangzhou Fuchun Bay New Town production base is expected to commence construction by the end of 2023, increasing the annual production capacity by an additional 2.4 million product units upon commencement of operation
— The Group will consider distribution of a final dividend to share the fruits of success with shareholders

For the six months ended 30 June 2023 (the "Reporting Period"), the Group experienced revenue growth of 18.2% to US$81.4 million. Total sales volume also increased to approximately 725,000 units, representing a 20.8% increase over the previous year. Gross profit rose by 22.1% to approximately US$58.3 million, with a gross profit margin of 71.6%. As a result, profit attributable to the owners of the Company reached US$25.2 million, an increase of 213.3%, with a net profit margin of 30.9%. Adjusted profit (non-HKFRS measure) (1) increased by 105.6% year-on-year to approximately US$25.4 million. Basic earnings per share amounted to US3.04 cents (2022 1H: US1.39 cents), while the diluted earnings per share was US3.03 cents (2022 1H: US1.20 cents). As at 30 June 2023, the Group was in a strong financial position with cash and bank balances of approximately US$239.0 million. (December 31 2022: US$229.1 million)

Mr. David Chien, Chairman, Executive Director and Chief Executive Officer of OrbusNeich, said, "Despite the global economic performance being dragged down by the continued tightening of monetary policies by the US and European central banks due to persistently high inflation, we are pleased that OrbusNeich has been able to maintain its growth momentum and achieve excellent results, thanks to our top-tier talents who are relentless in their pursuit of innovation and share our core values of 'Integrity, Passion, Innovation, and Performance'. As we progress, we are committed to broadening our distribution network, enhancing our R&D capabilities, diversifying our product lines, and expanding our production capacity. We are confident that these efforts will not only enrich our product portfolio and drive our business performance, but also benefit patients worldwide."

Demand from Key Markets Remains Strong
During the Reporting Period, the US market experienced remarkable growth of 61.6% year-on-year in revenue. In particular, sales of scoring balloons doubled in the US. Other markets, including Japan, APAC, EMEA, and the PRC, achieved year-on-year revenue (excluding foreign exchange impact) growth of 27.0%, 23.9%, 14.2%, and 8.2%, respectively, driven by the introduction of new generation products, and an increase in demand for related treatments. The growth was also due in part to an expansive sales network covering more than 70 countries and regions worldwide, a dedicated team of 147 sales and marketing personnel in 10 countries or regions and 217 distributors, as well as sales and marketing efforts. For example, the Group hosted three physical physician exchange programs to bring skilled physicians from Japan, Singapore and Australia to Vietnam and Malaysia to enhance the PCI/PTA skills and experience of local physicians, and organised or participated in around 30 seminars, workshops, conferences and discussion panels globally. All these initiatives increased the Group's exposure in its target markets.

Global Recognition for Outstanding R&D Capabilities and Product Excellence
As at 30 June 2023, OrbusNeich had an impressive portfolio of over 210 granted patents and published patent applications in key jurisdictions around the world, including over 30 and 55 granted patents in the US and the PRC, respectively, demonstrating its commitment to innovation. During the Reporting Period, the Group's new generation products not only saw significant growth in market share, but also received certifications and recognition in more key jurisdictions. As Europe transitioned from the Medical Device Directive (MDD) to the more stringent Medical Device Regulation (MDR) regime, the Group achieved its first MDR certification for the Scoreflex TRIO Balloon Dilatation Catheter. In addition, the Group successfully completed the renewal of CE certification for the Sapphire PTCA Family under MDR. It also obtained CE Mark for the EZ Guide Guiding Extension Catheter, NMPA approval for Sapphire Neuro balloon and PMDA approval for Teleport XT microcatheter. Meanwhile, progress was made on the Group's pipeline products, with the Scoreflex TRIO clinical trial commencing in the PRC in April 2023. The Group also submitted the Teleport XT microcatheter for FDA approval.

The Group continues to make breakthroughs in the use of new materials. For example, two upcoming coronary products, Sapphire Ultra and Sapphire Ultra NC, will apply the latest raw material technologies to reduce costs while maintaining excellent product performance. Both products are expected to receive FDA approval by the end of 2023. The economical balloon series will enable the Group to reach more developing countries with lower prices, making this life-saving technology more accessible to patients in developing countries and regions.

"Our joint venture, ON P&F, continued to redefine the structural heart product landscape through relentless innovation. From the active promotion of our first commercialized product, TricValve, to the submission of a clinical trial study protocol of TricValve to the NMPA, together with the comprehensive pipeline of interventional structural heart devices, we are confident of solidifying our market leadership position and building a healthier future for all," added Mr. Chien.

Expanding Production Infrastructure to Support Growing Demand
OrbusNeich owns production bases in the PRC and the Netherlands, as well as R&D centers in the PRC and the US. In order to meet the rapidly increasing demand for the Group's products, the Group has been working diligently to expand its production capacity. During the Reporting Period, new production machinery was installed at its Shenzhen facility and certain production processes were transferred to its newly leased premises in Fuyong Shenzhen. This new manufacturing site has passed ISO and NMPA inspections and has has been included in the ISO 13485 certification and China manufacturing permit. This facility is expected to bring the Group's total annual production capacity to 1.8 million balloon units and 60,000 stent product units, respectively.

In terms of medium to long-term production capacity planning, the Group has entered into a commercial agreement with the Hangzhou Fuchun Bay New Town Management Committee to establish an R&D and production base dedicated to vascular interventional medical devices. Subsequently, in June 2023, the Group successfully acquired a land parcel of close to 20,000 sq.m in Fuyang, Hangzhou for approximately RMB10.5 million. The Group intends to use this land to construct a state-of-the-art R&D and manufacturing facility covering an area of approximately 60,000 sq.m, which is expected to commence construction by the end of 2023 after obtaining the necessary construction permits. Upon completion, this facility is expected to increase the Group's production capacity by an additional 2.4 million units of products per year.

Looking ahead to the second half of 2023, OrbusNeich is fully confident of maintaining steady growth in both revenue and net profit through market penetration, expansion, and efficiency enhancement. The US market is expected to play a crucial role in the Group's growth strategy, as it expects to further expand its hospital coverage in this vast market as its US distributor has been recently acquired by Abbott. In the PRC market, the Group plans to diversify its product mix by promoting more new products. In addition to coronary balloons, this diversification will include a focus on microcatheters and peripheral products.

Mr. Chien concluded, "We are actively seeking merger and acquisition targets with innovative and high-caliber endovascular intervention products that can create synergies with our extensive distribution network. We are also exploring opportunities to expand our direct sales network with the aim of boosting the Group's revenue and profitability. As we strive to realize our vision of becoming a world-leading medical device developer and manufacturer, providing innovative and comprehensive endovascular and structural heart interventional solutions that effectively improve the quality of life for patients, we also place high value on providing returns to our shareholders and will consider distributing a final dividend to share our fruits of success."

About OrbusNeich Medical Group Holdings Limited
OrbusNeich is a major global medical device manufacturer specializing in interventional devices for percutaneous coronary intervention (PCI) and percutaneous transluminal angioplasty (PTA) procedures. Headquartered in Hong Kong, China, OrbusNeich sells its products in more than 70 countries and regions worldwide. It is also the only PCI balloon manufacturer headquartered in China that ranked among the top six players in all major overseas PCI balloon markets including Japan (No. 2), Europe (No. 4), and the U.S. (No. 6) in terms of PCI balloon sales volume in 2021, according to a CIC report. In addition, it ranked No. 3 in Japan and No. 4 in the U.S. in terms of PTA balloon sales volume in 2021. It also specializes in coronary stent products and is actively expanding into neuro vascular intervention and structural heart disease. As of June 30 2023, OrbusNeich has more than 210 granted patents and published patent applications worldwide. Its in-house R&D team has more than two decades of product development experience and has developed world-leading proprietary technologies.

For more information, please visit the Group's official website: https://orbusneich.com/

(1) Excluding certain non-cash and one-off items, including listing expenses, unwinding of interests on convertible redeemable preferred shares and share-based compensation expenses.


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Beverly Hills Based IMA ART Fertility Launches We Create Heirs Marketing Campaign Serving China’s Uber-Wealthy

BEVERLY HILLS, CA, Aug 17, 2023 – (ACN Newswire) – Patek Philippe Geneve is synonymous with the next generation. IMA ART Fertility helps its Chinese Clientele create the next generation through access to the world's finest network of specialists in the fields of fertility and reproductive law.


IMA ART Fertility Co-Founders
IMA ART Fertility provides a trusted avenue towards family creation.


Launching the first of its kind We Create Heirs(R) fertility & surrogacy campaign exclusively serving China's super wealthy, IMA ART embarks upon a truly unique adventure to capture the senses, imagination and desires of discreet high-net-worth families. IMA ART Fertility's singular focus is helping discerning Chinese clientele build their families – and the next generation – by utilizing the full suite of advanced assisted reproductive technologies, including gender selection, PGT (pre-implantation genetic testing), ICSI (Intracytoplasmic sperm injection) & surrogacy. California's progressive legal framework allows for any single person, LGBTQ and heterosexual couple to become parents – these are luxuries not legally available outside the U.S.

"Indeed, there can be no grander luxury than our children. IMA ART redefined a new paradigm in fertility," said Michelle Tang, CEO, Co-Founder & Ethnic Chinese.

Unfortunately, for many, this ultimate luxury requires a little help – that's where IMA ART Fertility's bespoke family journey comes in. The Co-Founders' imaginations know no limit when it comes to going above and beyond, with infinite creative freedom to design Chinese guests' ultra-personalized experience for the next generation. At IMA ART, nobody does what they do at the high level they do it.

Wealthy Chinese clients inherently understand having more children diversifies their generational risk. Wealthy Chinese families are pragmatic and understand competition between their offspring ensures the family's assets are ultimately passed down to that child with the most ability – offspring who will carry on the family lineage to future generations.

Having one child carries enormous risks for affluent Chinese families. If that offspring is incapable, it is believed the family will collapse. More children minimizes the risk, maximizes social development and the future success of the family over future generations. Chinese families have experienced many upheavals and challenges during their long history. IMA ART Fertility provides a trusted avenue towards successfully continuing the family bloodline.

Traveling across Hong Kong, Shenzhen, Beijing and Shanghai, Co-Founders Michelle Tang and Ron Sonnenberg have taken their case to the super private lives of China's mega-wealthy. Families who have achieved unimaginable success and who demand the very best in all their endeavors. This is especially important in the field of international fertility & surrogacy arrangements.

About the Company: Privately held IMA ART offers the first-of-its-kind significant, unique, and consistently elevated luxury fertility experiences to intended parents from around the world. The firm's bespoke professional advisory services provide transformative luxury concierge services paired with fertility & surrogacy in Beverly Hills. The company's exclusive suite of discreet fertility options is exclusively available to busy high-net-worth individuals. Learn more.

Contact Information:
Ron Sonnenberg
Co-Founder
ron@imaartfertility.com
(424)-284-1408

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

New CGFNS Survey of Immigrant Nurses in the U.S. Reveals Their Economic Impact

PHILADELPHIA, PA, Aug 16, 2023 – (ACN Newswire) – In addition to helping alleviate a chronic nursing shortage in the United States, immigrant nurses are estimated to spend well over $46 billion annually in the U.S. economy while providing hundreds of millions more in financial support to family members back home, according to a report from CGFNS International, a global leader in credentials evaluation services that support health worker mobility.




The Economics of Nurse Migration report is based on a survey of more than 1,500 foreign-educated nurses who have used the organization's credentials verification services to facilitate their migration to the U.S. The results offer a window into the economic experiences and impact of nurse immigrants working in the U.S., as well as the driving reasons for their migration.

The report can be downloaded from cgfns.org/eonm23.

"This report quantifies the financial costs and sacrifices associated with nurse migration while highlighting the substantial contributions that immigrant nurses make to host countries and the economies of both the host and sending nations," said Dr. Peter Preziosi, CGFNS International's President and CEO.

In the survey, the main reasons nurses cited for migrating were largely balanced across three key drivers – familial (31 percent), professional (29 percent) and economic (25 percent). In terms of their economic impact, the survey results showed:

The average salary for respondents was $65,700 within the first three years of arrival and $71,800 overall, compared with $89,000 average salary for registered nurses in the U.S. A quarter of respondents reported making more than $90,000 annually.

Immigrant nurses reported spending 60 percent of their income in their communities on housing, other necessities and local shopping, with another 25 percent for taxes.

Two-thirds (66 percent) send money home to friends and family on a regular basis – averaging about five percent of their spending. Of those that sent money, 44 percent reported sending home more than 10 percent of their monthly salary.

Extrapolating from other data showing there are 688,000 immigrants in the U.S. nursing workforce of more than 4.3 million, the CGFNS report estimates that after sending $1.6 billion in remittances to the communities they left, immigrant nurses spend at least $46.9 billion annually in the U.S. economy.

About half (52 percent) of nurse immigrants reported engaging a recruiter to handle their migration process. However, that proportion rises to 79 percent when narrowing the sample to those who migrated in the past three years.

Fifty-two percent of survey respondents who used a recruitment firm elected to use a Certified Ethical Recruiter (CER), a designation given to those firms that agree to additional oversight by CGFNS's Alliance for Ethical Recruitment Practices and comply with its ethical code.

"By illuminating these essential aspects of nurse migration to the United States, we aim to provide policymakers, healthcare leaders, and stakeholders with a comprehensive perspective that transcends mere statistics and embraces the inherent value of immigrant nurses to both America's health systems and economy," said Preziosi.

About CGFNS International, Inc.

Founded in 1977 and based in Philadelphia, CGFNS International is an immigration-neutral not-for-profit organization proudly serving as the world's largest credentials evaluation organization for the nursing and allied health professions. CGFNS International is an NGO in Consultative Status with the United Nations Economic and Social Council (ECOSOC) and is a member of the Conference of NGOs in Consultative Relationship with the United Nations (CoNGO). For more information, visit https://www.cgfns.org.

Contact Information:
Mukul Bakhshi, Esq.
Chief of Strategy and Government Affairs
mbakhshi@cgfns.org
(215) 243-5825

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Essex Bio-Technology Posts Sound 2023 Interim Financial Results, Revenue Up 37.1%, Profit Up 22%

HONG KONG, Aug 16, 2023 – (ACN Newswire) – Essex Bio-Technology Ltd ("Essex" or the "Group", Stock Code: 1061.HK) today announced the interim results for the six months ended 30 June 2023 ("the period under review").

Financial Performance Returned to Pre-COVID-19 Operating Level

During the period under review, the Group achieved a consolidated revenue of approximately HK$899 million, with an increase of 37.1% as compared to the same period last year, indicating normalcy in business to the pre-COVID-19 operating level. The profit of the Group increased by 22.0% to approximately HK$170 million as compared to approximately HK$139.2 million for the same period last year.

As of 30 June 2023, the Group had cash and cash equivalents of approximately HK$506 million (31 December 2022: approximately HK$543 million). The Board is pleased to propose an interim dividend of HK$0.045 (For the six months ended 30 June 2022: HK$0.04) per ordinary share for the six months ended 30 June 2023.

Revenue Growth in Ophthalmology and Surgical Segments

The Group's revenue is primarily made up of the segments of Ophthalmology and Surgical (wound care and healing). For the six months ended 30 June 2023, the revenue of Ophthalmology increased by 41.6% to approximately HK$382 million, accounting for approximately 42.4% of the Group's revenue, while the revenue of Surgical up 34.0% to approximately HK$518 million, representing approximately 57.6% of the Group's revenue. The core products that are as current growth driver under each segment are:

1. Ophthalmology – Beifushu series (Beifushu eye drops, Beifushu eye gel and Beifushu unit-dose eye drops), Tobramycin Eye Drops, Levofloxacin Eye Drops, Sodium Hyaluronate Eye Drops and Iodized Lecithin Capsules; and

2. Surgical (Wound care and healing) – Beifuji series (Beifuji spray, Beifuji lyophilised powder and Beifuxin gel), Carisolv dental caries removal gel, Dr. YaDian mouth wash,Yi Xue An Granules and PELNAC collagen-based artificial dermis.

Significant Business Development Activities

The Group is committed to pragmatically investing in new products and technologies to strengthen the Group's product and research and development ("R&D") pipeline as near to mid-term growth driver in ophthalmology and long-term plan for new therapeutics in oncology. During the period under review, major investments in ophthalmic products that are currently in an advanced stage of clinical development are outlined as follows:

Re-establishing the VISTA programme after the acquisition of SkQ1's intellectual property rights

In order to provide the Group with flexibility and independence in the continuing development of the US FDA VISTA programme in the field of dry eye disease and to allow the Group to explore further the development of products for other ophthalmic indications, the Group successfully secured a patent assignment deed and a patent and know-how licence agreement relating to SkQ1 in the field of ophthalmology from Mitotech.

Following the acquisition of the intellectual property rights relating to SkQ1 on 13 October 2022, the Group's priority is to complete the transfer of chemistry, manufacturing and controls (CMC), know-how and intellectual property rights relating to SkQ1 from Mitotech. Concurrently, the Group is re-establishing the VISTA programme with regulators for mitigating any identifiable risks before continuing with the clinical trial. According to Frost & Sullivan, the estimated number of patients with moderate-to-severe dry eye disease was around 119.7 million in the PRC in 2020. It is expected that the size of the potential market of the SkQ1 product will be significant.

EB12-20145P (HLX04-O) global phase 3 clinical study makes significant progress

In 2020, the Group entered into a co-development and exclusive licence agreement with Shanghai Henlius Biotech, Inc. to co-develop a pharmaceutical product (EB12-20145P), a recombinant anti-vascular endothelial growth factor ("anti-VEGF") humanised monoclonal antibody injection for the treatment of exudative (wet) age-related macular degeneration ("wet-AMD"). As at the date of this announcement, the product has been approved to commence phase 3 clinical trials in Australia, the United States, Singapore, Russia, Serbia and European Union countries such as Hungary, Spain, Latvia, the Czech Republic and Poland. So far, the first patient has been dosed in a phase 3 clinical study for EB12-20145P for the treatment of wet-AMD in the PRC, Latvia, Australia and the United States. Also, the phase 1/2 clinical study for EB12-20145P for the treatment of wet-AMD has shown its safety and tolerability and demonstrated preliminary efficacy.

In February 2023, the Group entered into an amendment agreement with Henlius to amend certain terms of the co-development and exclusive license agreement, which included payments for regulatory and commercial sales milestones and development costs in respect of the Anti-VEGF licensed product, details of which are in the announcement dated 22 February 2023 and the annual results announcement on 8 March 2023.

The Anti-VEGF Licensed Product can be used for treating wet-AMD, diabetic macular edema, macular edema caused by retinal vein occlusion and myopic choroidal neovascularisation. According to Frost & Sullivan, the estimated number of patients with these 4 categories of disease was around 15.8 million in the PRC in 2020. Assuming each patient applies 4 doses in the first year of treatment and 2 to 3 doses in subsequent years, it is expected that the size of the potential market of the Anti-VEGF licensed product will be significant.

Honors and Awards Obtained In 2023

Zhuhai Essex Bio-Pharmaceutical Company Limited, a wholly-owned subsidiary of the Group, has been recognised as one of the 2022 top 100 innovative companies in Zhuhai, and has also been recognised as one of the 2022 top 100 chemical pharmaceutical companies in the PRC. The Group's Beifushu has been awarded as one of the Chinese reputable medicine brands in five consecutive years. This is a testament to the recognition by the industry for the efficacy and quality of our flagship biologic drug.

Market Development Entrenched Market Access Capability

The Group has been relentlessly investing in establishing and strengthening its market access capability. As at 30 June 2023, the Group maintains a network of 43 regional sales offices in the PRC with a total number of more than 1,200 sales and marketing representatives, covering more than 12,100 hospitals and medical providers, coupled with more than 2,100 pharmaceutical stores, which are widely located in the major cities, provinces and county cities in the PRC. Sales to lower-tier cities is supplemented by on-line platform for medical consultation and e-prescription, the on-line platform is further deployed for serving patients with chronic diseases.

The Group's expansion of its market access into Southeast Asian countries via its base in Singapore has been gaining good development traction since 2020.

Research and Development

During the period under review, the Group remains focused executing its 5-year (2021 to 2025) R&D's development plans. As at 30 June 2023, there are 16 R&D programmes in the pre-clinical to clinical stage, out of which the following 4 ophthalmology programmes are as mid-term growth drivers:

— EB11-18136P: SkQ1 eye drops, second phase 3 clinical trial (US FDA) (VISTA-2) topline data released on 24 February 2021
— EB11-15120P: Azithromycin eye drops, ongoing review by external key opinion leaders (National Medical Products Administration ("NMPA") in the PRC)
— EB12-20145P: Bevacizumab for wet age-related macular degeneration ("wet-AMD"), phase 3 clinical trial (US FDA, European Medicines Agency, Therapeutic Goods Administration and NMPA in the PRC)
— EB11-21148P: Cyclosporine eye drops, phase 2 clinical trial (NMPA in the PRC)

The Group holds a total of 73 patent certificates or authorisation letters, which include 52 invention patents, 14 utility model patents and 7 design patents. The Group currently has diversified its R&D resources to multiple research sites in Zhuhai (PRC), Boston (United States), London (United Kingdom) and Singapore which support not only our pursuit of new therapeutics but also our recruitment of global talents.

Mr. Patrick Ngiam, Chairman of Essex, said, "With tenacity and strength, we are pleased to return our business performance to the pre-COVID-19 operating level. Barring any unforeseen circumstances, being resilient, relevant and growth ready, the Group is optimistic of delivering progressive results.

I would like to take this opportunity to express my sincere gratitude to all stakeholders, business associates and valued customers for the trust, support and cooperation accorded to us, and each and every member of the Group for their relentless efforts rendered in shaping the Group into being a progressive and promising pharmaceutical player."

About Essex (1061.HK)
Essex Bio-Technology Limited is a bio-pharmaceutical company that develops, manufactures and commercialises genetically engineered therapeutic b-bFGF (FGF-2), having six commercialised biologics marketed in China since 1998. Additionally, it has a portfolio of commercialised products of preservative-free unit-dose eye drops and Iodized Lecithin Capsules etc.. The products of the Company are principally prescribed for the treatment of wounds healing and diseases in Ophthalmology and Dermatology, which are marketed and sold through approximately 12,100 hospitals and managed directly by its 43 regional sales offices in China. Leveraging on its in-house R&D platform in growth factor and antibody, the Company maintains a pipeline of projects in various clinical stages, covering a wide range of fields and indications.


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Revolutionising Regenerative Medicine in Asia: A Landmark Collaboration between HealthPro Pharma, Fior Bioscience, and Medi Lifestyle

KUALA LUMPUR, Aug 16, 2023 – (ACN Newswire) – Medi Lifestyle Limited, a renowned Singapore-listed frontrunner in healthcare innovation, today unveiled a momentous collaboration between its indirect wholly-owned subsidiaries, HealthPro Pharma Pte Ltd (HPP) and Healthpro Marketing Sdn. Bhd (HPM), with FIOR Bioscience, LLC and Shine Bioscience, LLC (SBS).


Dato' Ken Low, Executive Director and Chief Executive Officer of Medi Lifestyle


This groundbreaking partnership promises to not only accelerate access to cutting-edge stem cell therapy products but to catalyse a revolution in healthcare, positioning regenerative medicine at the forefront of modern treatment across Asia.

The collaboration will meld the unique and complementary strengths of HPP, HPM, SBS, and Fior Bioscience, united by a shared vision of enhancing patient outcomes and breaking new ground in medical innovation. Fior Bioscience, with over a decade and a half of dedicated experience, stands as a perfect alignment to Medi Lifestyle's steadfast commitment to elevating healthcare standards through quality, innovation, and ethical practices.

Shine Bioscience, as the handpicked exclusive distributor for this collaboration's revolutionary stem cell therapy products, will capitalise on its far-reaching connections to Asia's elite laboratories, fuelling both research and development and streamlining distribution across the vibrant region.

Dato' Ken Low, Executive Director and Chief Executive Officer of Medi Lifestyle emphasised, "We aim to import and distribute FDA-registered stem cell therapy products and lead localised research and development efforts. By driving innovation and maintaining the highest safety and ethical standards, we dedicate ourselves to our patients' well-being and satisfaction."

Mr. David Kasteler, Managing Director of Shine Bioscience, added, "This collaboration signifies a milestone in making stem cell therapies accessible and effective in Asia. Together with Fior Bioscience's pioneering research and the patient-centric approach of Healthpro Pharma and Healthpro Marketing, we're committed to transforming healthcare across the region."

Medi Lifestyle's strategic move solidifies its stance as a leader in preventive healthcare. The partnership encapsulates an ethos of pioneering technology, uncompromising safety measures, and world-class expertise that converge to set new benchmarks in stem cell treatment options.

With registered offices and clinics extending their reach to Petaling Jaya, Malaysia, Medi Lifestyle continues to break barriers and redefine healthcare for the future.

Medi Lifestyle Ltd: https://www.medi-lifestyle.com/

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Kingworld Further Subscribed For 2.08% Equity of Taiko Pharmaceutical To Optimize Its Layout of Pharmaceutical Industry

HONG KONG, Aug 16, 2023 – (ACN Newswire) – Kingworld Medicines Group Limited ("Kingworld Medicines" or the "Group", stock code: 01110.HK), a leading healthcare distribution company, announced on 15th that the Group plans to further subscribe for the shares of Taiko Pharmaceutical Co., Ltd. ("Taiko Pharmaceutical," stock code: 4574.JP) at a price of 338.58 yen per share (equivalent to approximately 18.35 Hong Kong dollars). The additional subscription will involve 1,007,500 shares of Taiko Pharmaceutical and representing approximately 2.08% of the enlarged issued share capital of Taiko Pharmaceutical. The total consideration for this transaction value amounts to 341,119,350 yen (equivalent to approximately 18,488,669 Hong Kong dollars). After this acquisition, combined with the previously subscribed shares, the group will collectively totally hold 3,185,900 shares of Taiko Pharmaceutical, representing approximately 6.42% of the enlarged issued share capital of Taiko Pharmaceutical.

Established in 1946, Taiko Pharmaceutical is a renowned pharmaceutical company in Japan, specializing in manufacturing and sales of pharmaceutical products and infection management (sanitation control) products. A key asset of its portfolio is the famous and long-standing, "Taiko Seirogan" brand, renowned for its effectiveness and over 120 years of history. Since its establishment in 1996, Kingworld Medicine has been the sole general distributor of the Taiko Seirogan in China, significantly contributing to expanding the domestic sales volume of Taiko Seirogan. Notably, in the past two years, there has been a significant 64% domestic market growth in 2022. Over time, Taiko Seirogan has become one of the best-selling flagship product of the Group.

As a leading enterprise in the field of greater health dedicated to the import and distribution of branded pharmaceutical and healthcare products, the Group remains committed to investing in the pharmaceutical and health industry. The increased stake in Taiko aligns with the Group's Fifth Five-Year strategic plan and operational objectives. The Group will continue consolidating its existing business and actively expand its upstream supply chain traceability cooperation with partners such as Hong Kong Foci Pharmaceutical Co., Ltd. and Taiko Pharmaceutical. The Group will focus on building the Longde health industry ecosystem to establish a comprehensive supply chain system within the pharmaceutical and greater health industry, expanding the Group's industry footprint.

Mr. Zhao Lisheng, Chairman of Kingworld Medicines Group, stated, "After Kingworld Medicines Group acquired a stake in Taiko Pharmaceutical in April this year, synergies between the two parties have enhanced operational quality and efficiency. The Group is committed to deepening cooperation with Taiko Pharmaceutical and leveraging this additional subscription to foster mutual growth. After the acquisition, the Group will continue to strengthen its position in the market for Taiko Seirogan, consolidating its brand presence. In the future, the Group will also explore related resources of Japanese herbal medicine to enrich the company's product portfolio and cultivate new avenues for profit growth. Therefore, investing in Taiko Pharmaceutical will assist the company in optimizing its industry layout, preserving and promoting traditional Chinese medicine formulations, and ultimately contributing to public health advancement."

Furthermore, in 2021, Kingworld Medicines invested a 49% stake in and operated Foci Hong Kong in partnership with Lanzhou Foci. During the collaboration, the Minshan brand series of products within the Hong Kong market saw exceptional growth. In 2022, Kingworld Medicines Group acquired Innopharm in France, officially expanding its European market. This increased stake in Taiko Pharmaceutical propels the expansion of the Group's upstream supply chain, promoting strategic synergy across the industry chain and enhancing international brand competitiveness and sales scale.


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com