Overcoming Challenges to Biopharmaceutical Development and Manufacture with Science- and Risk-Based Strategies

The many challenges of biologic drug development and manufacturing cannot be resolved by a single company, and, because of this, IQ Consortium’s Biologics CMC Leadership Group and 10 other working groups have made it their mission to facilitate the identification of challenges that impede the development and/or commercial manufacture of biologic products, and to propose broadly applicable solutions to proactively advance innovative, science-, and risk-based strategies. Using a platform developed by the Consortium, the entity enables the pre-competitive exchange of information while addressing a variety of these challenges.

Read this article in Pharmaceutical Technology's Regulatory Sourcebook March 2021 eBook.

About the authors

Saroj Ramdas is GSK fellow and director, CMC regulatory strategy and advocacy with GlaxoSmithKline; Renata Varga is principal scientist, Teva Branded Pharmaceutical Products R&D, Inc; Martin Gastens is senior director program management, AbbVie Deutschland GmbH & Co. KG; Twinkle R. Christian is process development scientist, Bharat Jagannathan is process development senior scientist, and Barbara Rellahan*, rellahan@amgen.com, is director, product quality, all at Amgen; Jillian Brady is manager, science, regulation & policy, Faegre Drinker Biddle & Reath LLP; all authors are members of the IQ Consortium.

*To whom all correspondence should be addressed.

Article Details

Pharmaceutical Technology
eBook: Regulatory Sourcebook, March 2021
March 2021
Pages: 36–41

Citation

When referring to this article, please cite it as S. Ramdas, et al., “Overcoming Challenges to Biopharmaceutical Development and Manufacture with Science- and Risk-Based Strategies," Pharmaceutical Technology Regulatory Sourcebook eBook (March 2021).