Smartlab Europe

BD Biosciences Introduces CD4 Testing Product in collaboration with ReaMetrix That Does Not Require Refrigeration

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

– Leave Message for Us to Get Back

Related stories

Lilly Launches New AI Supercomputer for Drug Development

Eli Lilly has launched what it describes as the...

Advanced Analytical Technologies in Pharma Impurity Testing

Advanced analytical technologies in pharma impurity testing are transforming how trace contaminants are detected, identified, and controlled across the drug lifecycle. With high-resolution instrumentation, automation, and AI-driven insights, the industry is strengthening precision, data integrity, and patient safety to meet increasingly stringent purity standards.

Advancing Quality 4.0 Through Centralized Drug Knowledge 

Implementation of a unified data framework serves as the catalyst for modernizing pharmaceutical production, bridging the gap between legacy processes and intelligent automation. By consolidating disparate data streams into a cohesive repository, organizations achieve unprecedented visibility into critical quality attributes and process parameters. This transformation facilitates proactive risk mitigation and ensures that Good Manufacturing Practices are maintained through high-fidelity insights rather than retrospective analysis, ultimately fostering a culture of continuous improvement and operational excellence.
- Advertisement -

BD Biosciences, a segment of BD announced the creation of new dried reagents developed through a collaboration with ReaMetrix, a private biotechnology company based in Bangalore, India.  The new reagents, expected to be available in 2011, are developed for the BD FACSCount™ Flow Cytometry System, which is recognized as the system of choice for CD4 monitoring in global HIV/AIDS treatment programs because of its simplicity, robust performance and reliability. Bill Rhodes, President, BD Biosciences said, A key strategic driver behind the BD Global Health initiative focuses on expanding access to diagnostic products customized for use in developing settings. The ReaMetrix dried reagent helps us achieve this strategic objective because it does not require refrigeration, an amenity often unavailable in the developing world.  We are proud of our collaboration with ReaMetrix, which has brought forth an innovative product that expands access to CD4 testing in many remote, resource-limited locations.

CD4 testing assesses a patient’s immune system and guides clinicians in the proper administration of anti-HIV therapies.  Many countries, however, lack the necessary infrastructure to ensure the timely and reliable testing of patients with HIV/AIDS.

Difficulties in transporting, storing and using temperature-sensitive products and blood samples pose additional barriers to adequate, appropriate and cost-effective treatment in resource-limited settings. The new dried-down process expands access to CD4 testing in developing countries by eliminating the need for reagent refrigeration during shipment and storage.

ReaMetrix Chief Executive Officer Bala S. Manian, Ph.D said, At ReaMetrix, we are excited that our strategic collaboration with BD will result in the introduction of a product that will bring the benefits of CD4 monitoring to a much broader population in developing nations. The new dried reagent expands the reach of the BD FACSCount System, already the preeminent CD4 testing system in resource-limited countries.  By working together with BD, we are making new progress in making global health affordable and accessible.

About BD

BD is a leading global medical technology company that develops, manufactures and sells medical devices, instrument systems and reagents. The Company is dedicated to improving people’s health throughout the world. BD is focused on improving drug delivery, enhancing the quality and speed of diagnosing infectious diseases and cancers, and advancing research, discovery and production of new drugs and vaccines. BD’s capabilities are instrumental in combating many of the world’s most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs approximately 29,000 associates in more than 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, the pharmaceutical industry and the general public. For more information, please visit www.bd.com.

Latest stories

Related stories

Lilly Launches New AI Supercomputer for Drug Development

Eli Lilly has launched what it describes as the...

Advanced Analytical Technologies in Pharma Impurity Testing

Advanced analytical technologies in pharma impurity testing are transforming how trace contaminants are detected, identified, and controlled across the drug lifecycle. With high-resolution instrumentation, automation, and AI-driven insights, the industry is strengthening precision, data integrity, and patient safety to meet increasingly stringent purity standards.

Advancing Quality 4.0 Through Centralized Drug Knowledge 

Implementation of a unified data framework serves as the catalyst for modernizing pharmaceutical production, bridging the gap between legacy processes and intelligent automation. By consolidating disparate data streams into a cohesive repository, organizations achieve unprecedented visibility into critical quality attributes and process parameters. This transformation facilitates proactive risk mitigation and ensures that Good Manufacturing Practices are maintained through high-fidelity insights rather than retrospective analysis, ultimately fostering a culture of continuous improvement and operational excellence.

Quality Risk Management and the Role of Verified Drug Information

Effective quality risk management in pharmaceutical manufacturing hinges on the availability of verified drug information to ensure GMP compliance and product safety.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

– Leave Message for Us to Get Back

Translate »