Reliance Institute of Life Sciences

FDAnews Announces Quality, Compliance and Validation in the Digital Transformation Era Webinar Sponsored by Axendia & Tulip March 8, 2022

Retrieved on: 
Wednesday, March 2, 2022

With the productivity gains one will will make coupled with the digital acceleration brought about by COVID-19 changing course is a business imperative.

Key Points: 
  • With the productivity gains one will will make coupled with the digital acceleration brought about by COVID-19 changing course is a business imperative.
  • It will take the dread out of the transformation and empower one to modernize the systems and culture with new approaches to quality, compliance and validation.
  • Add to this the formation and structure of the FDA's new Office of Digital Transformation; it signals the serious stance the agency is taking on digital transformation.
  • With the regulators undergoing their own digital transformations and incentivizing life science companies to do the same it's time to move forward.

Global Research Antibodies Market Drivers 2021-2028 Include Rise In The Availability Of Technologically Advanced Products and a Rise In Proteomics And Genomics Research - ResearchAndMarkets.com

Retrieved on: 
Friday, December 3, 2021

The global research antibodies market size is expected to reach USD 5.9 billion by 2028.

Key Points: 
  • The global research antibodies market size is expected to reach USD 5.9 billion by 2028.
  • The market is expected to expand at a CAGR of 6.4% from 2021 to 2028.
  • Major market drivers include a rise in R&D initiatives undertaken by biopharmaceutical and biotechnology companies and government bodies, an increase in neurobiology and stem cell research, availability of technologically advanced products, and strategic collaborations among various key players.
  • Additionally, a rise in funds invested by pharmaceutical and biotechnology companies to enhance proteomics and genomics research is expected to boost market growth.

Moderna and the Institute for Life Changing Medicines Announce a New Collaboration to Develop an mRNA Therapeutic for Ultra-Rare Disease, Crigler-Najjar Syndrome Type 1

Retrieved on: 
Tuesday, September 7, 2021

The goal of the collaboration is to make an mRNA therapy for the treatment of CN-1 available at no cost to patients.

Key Points: 
  • The goal of the collaboration is to make an mRNA therapy for the treatment of CN-1 available at no cost to patients.
  • At Moderna, we believe that mRNA therapies have the potential to profoundly impact rare disease patients and their families.
  • In this innovative partnership, the Institute for Life Changing Medicines will not pay Moderna an upfront fee or any downstream payments.
  • The Institute for Life Changing Medicines believes that a healthy life is a basic human right.