CORRECTION BY SOURCE: Solta Medical’s Thermage(R) FLX and TR-4 Return Pad Receive Registration Certifications in China

LAVAL, QC, Jan 23, 2024 – (ACN Newswire) – Bausch Health Companies Inc. (NYSE/TSX:BHC) and Solta Medical, a global leader in the medical aesthetics market, today announced the approval of Thermage® FLX and the TR-4 Return Pad by China’s National Medical Products Administration (NMPA). [See *Correction above: The TR-4 Return Pad is not approved for use by the U.S. Food & Drug Administration.]

“The approval of Thermage FLX, and the TR-4 return pad, marks a significant milestone for Solta Medical,” Thomas J. Appio, Bausch Health Chief Executive Officer, said. “Not only is this important for growing our business, but it also represents an enormous achievement for our R&D and Regulatory Teams, who worked tirelessly with the NMPA.”

Thermage is a non-invasive treatment that uses radiofrequency technology to help tighten and improve the smoothness and texture of the skin’s surface to optimize a patient’s appearance. Thermage is a versatile and effective treatment that can be used on all skin types and genders, on a wide range of areas on the face, body and around the eyes. Globally, more than two million Thermage treatments have been performed.

“The approval from NMPA means we are able to continue the momentum of the growth of Thermage in China,” Jiny Kim, Senior Vice President, Solta Medical, said. “Building on the legacy of Thermage CPT, which has been serving Chinese institutions and consumers effectively since 2015, we look forward to delivering the Thermage FLX proven technology to the Chinese market.”

Indications

• The radiofrequency energy only delivery components of the Thermage® CPT and FLX system and accessories are indicated for use in:

o Non-invasive treatment of wrinkles around the eyes, including upper and lower eyelids

o Non-invasive treatment of wrinkles

• The simultaneous application of radiofrequency energy and skin vibration by the Thermage® CPT and FLX system and accessories are indicated for use in:

o Non-invasive treatment of wrinkles around the eye

o Non-invasive treatment of wrinkles

o Temporary improvement in the appearance of cellulite

Important Safety Information

Do not undergo Thermage treatment if you have a cardiac pacemaker, a cardioverter, a defibrillator, or any other electrical implant. Let your doctor know if you have an electrical implant or if you have any questions about whether you should undergo a Thermage® treatment.

Solta Medical has not studied the use of the Thermage system:

– Over skin fillers (lips, cheeks, facial wrinkles and skin folds)

– In people who are pregnant and/or breast feeding, diabetic, have an auto-immune disease such as lupus, have cold sores, have genital herpes, or have epilepsy

– In people who have permanent make-up and/or tattoos

– In children

The most commonly reported adverse effect during treatment is mild to moderate pain in the area being treated.

The most commonly reported adverse effects after treatment include the following:

– Mild redness may occur and typically resolves within 24 hours.

– Swelling may occur and typically resolves within 5 days but can remain up to several weeks.

The following adverse effects occur infrequently:

– The procedure may produce heating in the upper layers of the skin, causing burns and subsequent blister and scab formation. There is a possibility of scar formation.

– Skin surface irregularities may appear up to 1 or more months post-treatment.

– Numbness, tingling” or temporary paralysis may occur; typically resolves in a short period of time but may persist up to several weeks.

– Lumps or nodules may occur under the skin primarily in the neck area, and usually resolve within 1 or 2 weeks without chronic or long-term complications.

– Skin may darken, but normally resolves within several months.

Ask your doctor for more information about Thermage FLX and see www.thermage.com for additional details.

About Solta Medical

Solta Medical, a business unit of Bausch Health, is a global leader in the medical aesthetics market. Our vision at Solta is to develop and support trusted aesthetic brands that provide value to our customers and their patients. The Thermage® RF systems, Fraxel® laser, Clear + Brilliant® laser, and VASER® ultrasonic system provide exceptional results for patients and lasting growth to physicians due to our foundation of brands that have stood the test of time. More than five million procedures have been performed with Solta Medical’s portfolio of products around the world. More information can be found at www.solta.com.

About Bausch Health

Bausch Health Companies Inc. (NYSE/TSX:BHC) is a global diversified pharmaceutical company whose mission is to improve people’s lives with our health care products. We develop, manufacture and market a range of products primarily in gastroenterology, hepatology, neurology, dermatology, international pharmaceuticals and eye health, through our controlling ownership interest in Bausch +Lomb. With our leading durable brands, we are delivering on our commitments as we build an innovative company dedicated to advancing global health. For more information, visit http://www.bauschhealth.com and connect with us on Twitter and LinkedIn.

Forward-looking Statements

This news release may contain forward-looking statements about the future performance of Bausch Health, which may generally be identified by the use of the words “anticipates,” “hopes,” “expects,” “intends,” “plans,” “should,” “could,” “would,” “may,” “believes,” “subject to” and variations or similar expressions, including statements about the expected results of, and market for, the Company’s Thermage® treatment. These statements are based upon the current expectations and beliefs of management and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Actual results are subject to other risks and uncertainties that relate more broadly to Bausch Health’s overall business, including those more fully described in Bausch Health’s most recent annual report on Form 10-K and detailed from time to time in Bausch Health’s other filings with the U.S. Securities and Exchange Commission and the Canadian Securities Administrators, which factors are incorporated herein by reference.



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The 2024 TIENS Global Business Launch Conference Provides a Grand Opening

TIANJIN, China, January 18, 2024 – (ACN Newswire) – ‘HELLO TIENS, HELLO 2024’, TIENS Global Business Launch Conference was held at the TIENS International Health Industrial Park in Tianjin, China, on January 14.

 

 

Mr. Li Jinyuan, Chairman of TIENS Group, delivered the opening keynote, stating that TIENS would cooperate with technology giants such as Microsoft, Amazon, Huawei and Tencent to implement a comprehensive digital transformation. As an essential part of this transformation, the ‘V-Moment’ was released. V-Moment’s ‘intelligent’ education platform has a global footprint and allows distributors to receive professional training anytime, anywhere, regardless of language or region.

Another release was the ‘perfect’ supply chain system, the ‘Flying Lion Supply Chain’, designed to improve the efficiency and competitiveness of the Group’s global business operations. Additionally, as a global multinational enterprise, the TIENS Group launched a global resource-sharing platform, ‘MetaPoint Global Elites Club’, relying on its global advantages to join hands with elites in various fields worldwide to contribute to global sustainable development.

Closing the conference, TIENS Group presented a solemn flag ceremony to encourage all major business divisions to forge ahead in 2024. In the new year, TIENS will continue to uphold its mission of “Healthy Mankind and Serving Society”, actively embrace and master AI technology, and join hands with families worldwide to share a better tomorrow.

Media Contact

Ms Liang, TIENS Group
Email: liangyi1@tiens.com
Website: www.tiens.com

About TIENS Group

TIENS Group was founded in 1992 by Mr Li Jinyuan in Tianjin, China, joining international markets in 1995. During these years of development and self-transcendence, TIENS has become a global enterprise spanning biotechnology, health management, hospitality and tourism, education and training, e-commerce and international trade. With business covering 224 countries and territories and branches established in 117, the Group has achieved global business coverage and has formed strategic alliances with many first-class companies worldwide.

From TIENS International Health Industrial Park, the Group has formed a global health industry network involving a health science and technology innovation system, health production and logistics system, customer support system, health education system, and health investment and financial system, gathering talent flow, logistics, capital flow and information flow.  This global industrial chain covers a supply chain, a centralized product procurement system and a global network system with a shared e-commerce platform for its million-level membership and nearly 50 million family users.



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Envision Pharma Group Welcomes Industry Veteran and HR Expert Carolyn Bartholdson as Chief People Officer

FAIRFIELD, Conn., Jan 18, 2024 – (ACN Newswire) – Envision Pharma Group (Envision) has appointed Carolyn Bartholdson as its new Chief People Officer and member of the Executive Leadership Team.

“We are thrilled to welcome Carolyn, who’s proven herself as a people-leading expert in the life sciences industry, to Envision as our new Chief People Officer,” says Howard Miller, CEO of Envision Pharma Group. “Her strategic vision aligns seamlessly with ours, and her exceptional leadership experience will play a crucial role in securing and retaining top talent to support our growth.”

Carolyn’s extensive experience and industry background were most recently put to use in her Chief Human Resources role at Omnicom Health Group, where she led a global team overseeing human resources strategy and operations for the healthcare division of Omnicom. In this role, Carolyn completed multiple company HR integrations and created a mobility program to retain top talent. Her additional experience leading global company initiatives includes leadership roles with Pfizer, Barclays Wealth, and QBE North America.

“I am excited to bring my talents to such an innovative and progressive company as Envision Pharma Group,” adds Carolyn. “This is a unique opportunity for me to help accelerate the trajectory of an incredibly talented group of smart and dynamic individuals in the life sciences, an industry I love.”

About Envision Pharma Group:

Founded in 2001, Envision Pharma Group is a leading global technology-enabled strategic solutions partner for the life sciences industry, working with over 200 pharma and biotech companies, including 19 of the top 20 pharmaceutical companies. Envision supports clients across the product life cycle through a comprehensive suite of services and industry-leading technology solutions that include artificial intelligence and natural language processing, commercialization and integrated strategic consulting, evidence-based scientific communications and engagement, HEOR/market access and data analytics, medical capabilities, and omnichannel solutions. Learn more at www.envisionpharmagroup.com

Contact Information:
Colleen Carter
Associate Director, Communications, Office of CEO
colleen.carter@envisionpharma.com
1 (508) 505 8856



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Chiron AS Establishes State-of-the-Art Research Centre in Trondheim, Norway, Advancing Environmental Surveillance

TRONDHEIM, NORWAY, Jan 17, 2024 – (ACN Newswire) – Chiron AS, a leading producer of chemical reference materials headquartered in Trondheim, Norway, is pleased to announce the establishment of a state-of-the-art research centre dedicated to the enhanced surveillance of environmental pollutants. 

This ground-breaking development, supported by an estimated 40 million NOK investment, reaffirms Chiron’s commitment to advancing the field of environmental analysis. 

The newly inaugurated research facility, which offers a 360-degree view of the Trondheim fjord, is equipped to address the most challenging pollutants of today, including microplastics and PFAS (commonly known as ‘forever chemicals’), and is poised to contribute significant research into environmental surveillance. 

This strategic relocation follows Chiron’s acquisition by Antylia Scientific in July 2023 and its successful incorporation into the ZeptoMetrix® Operating Division. The move to the new 1750 m2 premises aligns Chiron with Spex®, NSI Laboratories and High Purity Standards in strengthening the ZeptoMetrix Reference Material and Proficiency Testing portfolio. 

“We are excited to embark on this journey of heightened environmental surveillance,” Jon Eigill Johansen, Founder of Chiron AS, commented. “The establishment of our research centre highlights our commitment to scientific excellence. Through cutting-edge research and collaboration, we aim to support our mission to protect humans from undesired chemical exposure.” 

Evangeline Gonzalez, President of the ZeptoMetrix Operation Division, stated, “This investment reinforces our dedication to advancing environmental science. Chiron’s state-of-the-art research centre adds a crucial dimension to the ZeptoMetrix portfolio. This means we are even more ready to support our lab and industry partners with critical innovation as they work to address ongoing environmental challenges.” 

About ZeptoMetrix® 

ZeptoMetrix, an Antylia Scientific Company, is the industry leader and manufacturer for innovative solutions solving challenges in the evolving Diagnostic Microbiology Infectious Disease, Oncology market and Analytical Reference Materials for the Applied Markets. We focus on our customers’ success by providing premium product quality, reliability, and expert technical knowledge, enabling our customers to develop and advance many applications across diagnostics, pharmaceutical, environmental, food and beverage industries. From in stock solutions to custom control and panel development through to launch, our scientific teams provide our customers with comprehensive, performance-oriented, and cost-effective products and services that positively impact the field of clinical diagnostics, analytical testing and contribute to a healthier world. ZeptoMetrix is an operating division of Antylia Scientific, a holding company of premier life science and diagnostic brands, including Cole-Parmer, Environmental Express and ZeptoMetrix.

Contact Information
Jennifer Button
Deputy Director
jenny.button@chiron.no 
+44(0)7963508499

Related Files

Chiron AS Establishes State-of-the-Art Research Centre.pdf

 

View the original press release on newswire.com.



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Revolutionizing Drug Development: Novigenix Unveils AI-Powered RNA Analysis for Immune Response Profiling

GENEVE, CH, Jan 17, 2024 – (ACN Newswire) – With cancer projected to escalate to 29 million cases by 2040[1], Novigenix, a pioneer in AI healthcare solutions, is rewriting the rules of cancer care. Their newest innovation, LITOSeek™, is primed to reshape drug development, offering a transformative leap forward.

From left: Dr. Brian Hashemi, Novigenix’s CEO and Chairman, Dr. Sahar Hosseinian, Co-founder & CTO, and Dr. Pedro Romero, Chief Medical & Scientific Officer

Personalized Cancer Treatment: Breaking Barriers

Every cancer is as unique as the person it affects. Tumors are in continuous dynamic interplay with the patient’s immune defenses and are adept at subverting and escaping immune control. Novigenix is on a mission to improve the cancer treatment landscape, leveraging advanced AI and RNA analysis from a routine blood draw to provide more precise insights into patient immune responses to cancer treatments, compared to conventional DNA liquid biopsies that evaluate tumor evolution through circulating tumor DNA (ctDNA). Insights into the precise dynamic of patient immune response thus pave the way for superior therapeutic discoveries in the field.

Empowering Biopharma: Unveiling LITOSeek™ at Precision Medicine World Conference

On January 24th at the Precision Medicine World Conference in Silicon Valley, Novigenix will debut LITOSeek™, a groundbreaking solution designed to expedite drug development for biopharma companies.

AI and RNA Analysis: Pioneering Healthcare Transformation

With a decade-long track record, Novigenix successfully launched Colox® blood test in Switzerland, powered by AI and RNA analysis to detect early-stage colon cancer, marking a significant departure from invasive colonoscopy procedures. By aggregating data from diverse colon cancer patients, Novigenix identified immune system biomarkers crucial for early-stage detection, enhancing treatment outcomes.

Dr. Brian Hashemi, Novigenix’s CEO and Chairman, emphasized, “Our experience with Colox® underscores the potential of AI RNA analysis. Ongoing studies across various cancer types have fuelled our Knowledge Base to uncover comprehensive sets of biomarkers via liquid biopsy and AI RNA analysis. Our validated immunotherapy response biomarkers provide early prediction of patient response and we invite biopharma companies to leverage our platform for more efficient and effective drug development.”

Professor Pedro Romero, M.D. Chief Medical & Scientific Officer of Novigenix, and Founding Chief Editor of the Journal of Immunotherapy of Cancer, highlights the importance of patient immune response in the development of novel therapies: “AI RNA analysis is poised to revolutionize healthcare, accelerating conventional experimental drug development with data-driven precision immune response prediction. By swiftly analyzing systemic immune responses, AI compresses analysis times, expediting traditional drug development and powering discovery of novel therapy targets.”

A Team Dedicated to the Future of Cancer Care

With over 20 Ph.D.-level scientists focused on the development of the LITOSeek™ platform and advancing next-generation liquid biopsy solutions, Novigenix is pioneering precision immunology to help transform cancer treatment paradigms for better patient outcomes.

[1] https://canceratlas.cancer.org/the-burden/the-burden-of-cancer/

Contact Information
Edwin Shankar
edwin.shankar@leidar.com

SOURCE: Novigenix

.

View the original press release on newswire.com.



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Envision Pharma Group Appoints Life Sciences Industry Veteran Alice Choi as President, Integrated Medical Capabilities and Solutions (IMC)

HORSHAM, UK, Jan 16, 2024 – (ACN Newswire) – Envision Pharma Group (Envision) has appointed Alice Choi as President, Integrated Medical Capabilities and Solutions (IMC) and a member of its Executive Leadership Team. In her new role, Alice will lead the organization’s IMC division made up of experts in medical strategy, medical communications, publications planning and delivery, patient engagement, and more to deliver smarter, faster outcomes for life sciences clients.

“I am so pleased to welcome Alice to the Envision team and her invaluable experience as a global life sciences industry leader,” shares Howard Miller, CEO of Envision Pharma Group. “Alice brings a depth of strategic expertise, knowledge, and insight in the medical communications, scientific research, and publications field that will be instrumental in propelling our vision forward for our people and serving the needs of our clients.”

Alice joins Envision from IPG Health where she most recently served as EVP, Managing Director, Client Solutions, APAC. Prior to this, the bulk of her career was in IPG Health Medical Communications – latterly as Chief Operating Officer for the group and formerly, as Head of Complete Medical Communications. During her tenure, she played a pivotal role in establishing and fulfilling long-term business goals while focusing on building upon key client relationships to foster sustained business growth, development, and operational excellence across several global teams. 

Alice is committed to best practices and standards in medical communications, as demonstrated in her current role as Chair of the Healthcare Communications Association and through her success at IPG Health Medical Communications and former tenure as Chair of the International Society of Medical Publications Professionals (ISMPP).

Alice adds, “I have long admired the work done by Envision and am excited to be joining such a stellar team. Medical communications continue to move at a rapid pace, and I look forward to ensuring that we continue leading the field in terms of our people, our quality, and our innovative patient-centric services.”

About Envision Pharma Group

Founded in 2001, Envision Pharma Group is a leading global technology-enabled strategic solutions partner for the life sciences industry, working with over 200 pharma and biotech companies, including 19 of the top 20 pharmaceutical companies. Envision supports clients across the product life cycle through a comprehensive suite of services and industry-leading technology solutions that include artificial intelligence and natural language processing, commercialization and integrated strategic consulting, evidence-based scientific communications and engagement, HEOR/market access and data analytics, medical capabilities, and omnichannel solutions. Learn more at www.envisionpharmagroup.com.

CONTACTS
Colleen Carter
Associate Director, Communications, Office of CEO
colleen.carter@envisionpharma.com
1 (508) 505 8856



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Hyris Fulfils Its Integration Into Ulisse Biomed to Give Birth to a New International Group Ready to Make Its Mark in the Global Biotech Market

LONDON, Jan 15, 2024 – (ACN Newswire) – A new international biotech group was born from the integration of Hyris Ltd, an innovative biotech company renowned worldwide for its disruptive genetic testing platform, and Ulisse Biomed S.p.A., also known as UBM Group or “UBM” only, an Italian-based publicly traded biotech company appreciated for its innovative testing platforms. 

Hyris Ulisse Corporate Integration - A new benchmark in the biotech market
Hyris Ulisse Corporate Integration – A new benchmark in the biotech market

As anticipated on December 4th, the integration between Hyris and Ulisse Biomed was officially ratified on December 21st by completing a reverse take-over operation and following the shareholders’ meeting of Ulisse Biomed held earlier on that same day, which also deliberated an increase of capital in option. The overarching goal is to give life to a new Italian segment of excellence in genetic analysis based on strong innovation competencies and ready to address international markets at scale.

The new Group, with strong roots in diagnostics, teranosis and healthcare, aims to create a strong actor operating as a leader in the in-vitro diagnostics industry, particularly molecular biology, thanks to flawless interoperability between its leading technologies. 

Matteo Petti, CEO of Ulisse Biomed, who will keep his role of managing director in the new corporate structure, is very positive about the whole operation, highlighting how its implications go way beyond a mere financial transaction: “We are excited to announce the integration with Hyris. By joining forces, we will enhance our product offering, combining our experience and development capabilities with Hyris’ unique mix of competencies. This integration aims to capitalise on the synergies between the two companies, maximising value for our shareholders and offering unprecedented integrated diagnostic solutions to our customers.” He concludes: “The success of this operation projects us towards new horizons, and the joint management will work immediately to leverage the new strategic synergies.”

The new structure aims to provide an integrated array of high-end performance products at a competitive cost to meet a diverse industry demand across various markets, defining a new portfolio of distinctive analytical capabilities at a global level

Stefano Lo Priorefounder of Hyris and former CEO and recently appointed Chairman of UBM Group, agrees: “We are proud of this integration between Ulisse Biomed and Hyris. We have a joint industrial project with a strong vision and have already received excellent feedback from the market regarding the joint proposition of our solutions. As a united company, we will be able to implement the project in a synergic manner and create a unique and distinctive offer on the global and, even more so, on the Italian biotech scene.” Priore is confident about the positive outcome of this operation: “Hyris and Ulisse Biomed are now officially part of the same team, united by common values and vision and a unique industrial. We are ready for the challenges that await us, strong of the competencies that the two companies will be able to pool together.”

In the next months, the new management will put into action a strategic plan to accelerate team and resource integration, leveraging the two companies’ similar cultures and shared values. 

For more information, feel free to write an email to info@hyris.net

Contact Information
Gabriele Salaris
Global Experience Manager
gabriele.salaris@hyris.net
+39 345 555 3379 

Source: Hyris



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Avance Clinical: Latest Analysis Reveals 65% of US Biotechs Struggle to Identify Suitable CRO Partner

SAN FRANCISCO, CA, Jan 9, 2024 – (ACN Newswire) – Avance Clinical, the leading Australian and North American CRO for biotechs announced today that new industry analysis shows 60-65% of US biotechs face challenges identifying the right sized CRO partner that can deliver at every phase of their drug development program. The report found this directly affected clinical programs and budgets.

View the report here

The report also found that 50% of biotechs engaged with more than one CRO over the course of their clinical program potentially impacting knowledge transfer, timelines and budget.

The new analyst report from Frost & Sullivan examined the challenges biotechs face during the CRO selection process saying “biotechs are increasingly wanting to partner with mid-sized, agile, and responsive CROs with a proven ability to rapidly advance quality clinical programs”.

“There is a perception among biotechs that large multinational CROs are less responsive and unable to adapt to the fast-paced nature of biotech demands,” according to the report.

Additionally, it noted that biotechs currently faced multiple challenges including a decline in biotech funding, a rise in drug development complexity, evolving FDA regulatory review processes, and costly delays caused by slow patient recruitment.

The report concluded that biotechs, especially those aiming to meet investor milestones, need to select the right CRO from the start.

The report outlined the key criteria US-biotechs use to identify the right CRO including:

1.    Established site relationships
2.    Scientific excellence 
3.    Quality compliance and data excellence
4.    Cost competitive
5.    Patient recruitment solutions
6.    Agile and responsive 
7.    Accelerated timelines
8.    Regulatory approval track-record
9.    Ability to expand to multi-regional global phases
10.    Access to latest technologies (including Artificial Intelligence & Machine Learning)

The report emphasized that biotechs were seeking CROs with established site relationships and highlighted that Avance Clinical now has more than 1,250 US-based sites in their GlobalReady Site Partnership Program to support US biotechs accelerate their clinical trials.

Each site has been accredited by Avance Clinical for data quality, patient centricity, and streamlined processes designed meet rigorous clinical timelines.

In addition, the report found a regulatory affairs track-record was a key selection criteria saying in-house regulatory expertise was the most attractive option for biotechs. It found that Avance Clinical is one of the only Australian/US mid-sized CRO with an inhouse regulatory affairs team experienced in FDA, EMA and China FDA approval processes.

Avance Clinical presented the report at JPM and Biotech Showcase 2024 where the team is taking meetings.

Avance Clinical has been recognised by Frost & Sullivan for the past 4 years with the prestigious Frost & Sullivan Asia-Pacific CRO Best Practices Leadership Award.

CEO Yvonne Lungershausen said “We have shown, with our high growth and industry-leading repeat business rates that our focus on gold standard technology paired with solution-orientated clinical experts is the mix our biotech clients need for clinical success”.

“Avance Clinical’s GlobalReady model is designed to extend biotechs’ investments so they can achieve greater clinical development milestones with reduced spend, all with the assurance of FDA accepted data,” she said.

GlobalReady gives our biotech clients conducting their early phase studies in Australia and New Zealand a seamless journey into the US to continue their clinical development programs, retaining the same high-quality CRO, which reduces time and cost and delivers quality FDA accepted data.

GlobalReady also enables US biotechs to conduct their mid to late phase studies in the US and expand to multi-regional locations.

In addition, the attractive 43.5% rebate on clinical spend in Australia, offers clients the opportunity to utilize our North American operations expertise and team, whilst maintaining services in Australia to maximise their rebate potential.

Find out more:

About Avance Clinical

Avance Clinical is the largest premium full-service Australian and North American CRO delivering quality clinical trials, with globally accepted data, in Australia, New Zealand and the US for international biotechs. The company’s clients are biotechs completing Phase I to Phase III of their drug development program that requires fast, agile, and adaptive solution-oriented clinical research services.

Frost & Sullivan Awards

Avance Clinical, a Frost & Sullivan Asia-Pacific CRO Market Leadership Award recipient for the past four years, has been providing CRO services in the region for more than 26 years.

Pre-clinical through to mid to late phase

Avance Clinical offers pre-clinical services with their experienced ClinicReady team right from pre-clinical through to Phase III clinical services leveraging significant Australian Government incentive rebates of up to 43.5% and rapid start-up regulatory processes.

With experience across more than 120 indications, the CRO can deliver world-class results and high-quality internationally accepted data for FDA and EMA review.

Technology

Avance Clinical uses state-of-the-art technology and gold standard systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, TrialHub, Certinia, Salesforce, Zelta and Medrio are just some of the technology partners.

www.avancecro.com

Media Contact:
Avance Clinical
Kate Thompson
media@avancecro.com



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Nutrigene Launches Personalised Development Program to Intersect Genetics and Learning through DNA

KUALA LUMPUR, Jan 8, 2024 – (ACN Newswire) – Nutrigene Modern Sciences Sdn. Bhd. (“Nutrigene” or the “Company”), a pioneer in the field of science-driven approach for child development, proudly announces the nationwide launch of Personalised Development Program (PDP). Representing a paradigm shift in parenting and education, this initiative harnesses the power of DNA to harmonize nature and nurture, fostering the holistic development of children.

L-R: Joyce Chan, MD of Nutrigene Modern Sciences; Dato Dr, Gavin Voon; Dato Sri Chuah Poh Khiang; Benjamin Yuen, TVB artist; ⁠Dr Choo Wenxi, Founder & CEO of Nutrigene Modern Sciences; Shaun Tam, TVB artist; ⁠Dato Sri Tommy Lee; ⁠Tyler Teh, Director of Nutrigene Singapore; and ⁠Carven Chan, Director of Educational Program
L-R: Joyce Chan, MD of Nutrigene Modern Sciences; Dato Dr, Gavin Voon; Dato Sri Chuah Poh Khiang; Benjamin Yuen, TVB artist; ⁠Dr Choo Wenxi, Founder & CEO of Nutrigene Modern Sciences; Shaun Tam, TVB artist; ⁠Dato Sri Tommy Lee; ⁠Tyler Teh, Director of Nutrigene Singapore; and ⁠Carven Chan, Director of Educational Program
TVB artists sharing experiences on their children’s DNA report with Dr Choo Wenxi, Founder & CEO of Nutrigene Modern Sciences
TVB artists sharing experiences on their children’s DNA report with Dr Choo Wenxi, Founder & CEO of Nutrigene Modern Sciences

Dr. Choo Wenxi, Founder & CEO of Nutrigene, emphasises the transformative nature of the program, “We’re committed to transforming the concept of parenting through the power of DNA. PDP is more than an educational program, it’s a comprehensive approach to nurturing children’s psychological well-being alongside their academic growth. Our goal is to assist families in understanding and supporting their child’s unique needs holistically, thereby shaping their futures.”

PDP is designed to catalyse a shift in educational paradigms, focusing on the psychological as well as the academic development of children. The program is designed to nurture diverse developmental domains, encompassing language, numeracy, world discovery, motor skills, arts and music. Aligned with forward-thinking families, educators, and childcare professionals, Nutrigene envisions a more informed and comprehensive approach to child development, fostering collaborative ventures to empower educators and parenting coaches to excel in their fields.

Dr. Choo added, “Our hallmark RIASEC (Realistic, Investigative, Artistic, Social, Enterprising And Conventional) Career Talent DNA Test has been innovatively applied to early childhood development. This framework enables parents to comprehend their child’s inherent strengths and inclinations from a young age, facilitating more informed and supportive parenting.

Nutrigene is proud to offer both RIASEC Career Talent DNA Test and PDP as a holistic solution for parents. We aspire to assist 10,000 families to recognize that every child deserves to develop physically, mentally and academically in their unique way by 2025. We are open to collaborations with individuals and organisations who share our vision of unlocking the full potential of every child through innovative and personalised education.”

In tandem with the launch of the PDP, Nutrigene announces the inauguration of its maiden branch in Kuching, Sarawak. Beyond business expansion, this move underscores Nutrigene’s commitment to democratizing their innovative educational approach, ensuring every child receives an education tailored to their unique needs, shaping a brighter and fulfilling future.

With the introduction of the PDP and the opening of a new branch in Sarawak, Nutrigene is poised to redefine the standards of personalized education, showcasing unwavering dedication to nurturing and empowering the next generation to thrive in an ever-changing world.

Dr. Choo said, “Ensuring qualified and compassionate educators at our center is crucial. Nutrigene values each educator, acknowledging their pivotal role in shaping young minds, and is committed to enhancing their professional journey, offering career advancement opportunities and personal growth. We aim to create a nurturing environment where educators feel respected, supported and empowered to deliver their best.”



Copyright 2024 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Spiden Announces Breakthrough in Non-Invasive Glucose Monitoring, Adds Key Executive Hires and Secures $15m in Additional Funding

PFAFFIKON, SWITZERLAND, Jan 6, 2024 – (ACN Newswire) – Spiden, a pioneer in non-invasive biomarker monitoring technology, is thrilled to announce a significant scientific milestone, key additions to its executive team and an oversubscribed convertible note.

Spiden's latest non-invasive glucose measurement campaignSpiden’s latest non-invasive glucose measurement campaignSpiden’s latest glucose measurement data comparing its non-invasive portable device (y-axis) with the invasive gold-standard (x-axis), illustrated in the Clarke Error Grid.

Spiden has achieved remarkable scientific progress in non-invasive glucose sensing. Utilizing advanced spectroscopy techniques in a portable device, its team has attained a 9% MARD with individual calibration (Mean Absolute Relative Difference – the average difference to the gold-standard measurement). This achievement is the latest important step towards a calibration-free and miniaturized device for non-invasive glucose monitoring. Now, as the final step on its development path, Spiden has commenced measurements in diabetes centers in multiple countries, before aiming to launch its Spiden wearable that can automatically calibrate to its customers without any needle involved.

“This accomplishment reinforces our commitment to launching our own glucose monitoring wearable by the end of 2025, followed by expanding to additional biomarkers,” says Leo Grünstein Spiden’s Founder & CEO. “We aim to help customers around the world take control of their health through non-invasive access to real-time biomarker data and actionable, evidence-based insights to improve their well-being and longevity.”

On entering this new phase towards product launch, the following key executives are joining the Spiden leadership team, bolstering its capabilities in design and product development.

– Chester Chipperfield, joining as Chief Design Officer, brings a wealth of experience from his previous roles as Head of Special Projects at Apple and Global Creative Director at Tesla. Chester’s expertise in innovative design and launching category defining products will be instrumental in shaping Spiden’s wearable into something that is both highly functional and desirable.

– Ismene Grohmann, has been appointed as Chief Product Officer. With her background as Head of Product for Abbott’s Consumer Biowearables and Global Innovation Director Personal Health, Ismene will lead Spiden’s product vision, strategy and execution, ensuring that Spiden’s solutions meet the highest standards of product-market fit, user-centricity and efficacy for its customers.

– Prof. Fernando Perez-Cruz, will be joining Spiden full time as Head of Machine Learning Research & AI. His background as Chief Data Scientist at the Swiss Data Science Center (joint venture between EPFL and ETH Zurich) uniquely positions him to shape Spiden’s advanced data analysis and AI capabilities.

Furthermore, Spiden has finished 2023 with a successfully secured $15 million convertible note, surpassing its initial target of $10 million, and bringing Spiden’s total funding since inception to >$40m. This achievement reflects the strong support from its existing investors and Board members, as well as new investors. This funding will help Spiden finalize its initial, now 6-year long phase of R&D, aimed at cracking complete calibration-free monitoring, as well as securing a pathway to miniaturization of its portable product to a wearable format. A larger funding round is planned for H2 in 2024, which will provide Spiden with sufficient capital to bring its product to market and become profitable.

About Spiden:

Founded in 2017 by serial entrepreneur Leo Grünstein, Spiden is a Swiss deep-tech startup dedicated to revolutionizing the field of personalized health monitoring. It employs a team of >70 staff, including >50 PhDs and university professors, operating out of its lab facilities in Pfäffikon SZ, Switzerland. Its unique approach combines advanced spectroscopy techniques and machine learning to achieve real-time, non-invasive monitoring of various biomarkers. Spiden’s mission is to forge a future where continuous health monitoring, using a Spiden wrist-worn wearable, becomes the norm, facilitating prevention and early detection, by empowering users with personalized control over their health and longevity.

Contact Information
Leo Grünstein
Founder & CEO
press@spiden.com

Related Images

Spiden's latest non-invasive glucose measurement campaignSpiden’s latest non-invasive glucose measurement campaignSpiden’s latest glucose measurement data comparing its non-invasive portable device (y-axis) with the invasive gold-standard (x-axis), illustrated in the Clarke Error Grid.
Spiden’s Founder & CEO Leo Grünstein using Spiden’s demo product to measure his glucose fully non-invasively through his wrist.

SOURCE: Spiden AG

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