biomanufacturing
The changes set to disrupt biopharma manufacturing in 2020
July 23 by Pharma IQWe speak to Elanco, Bayer, Janssen and Ipsen to find out what they think will be the biggest changes in the industry over the next year
[Analysis] How Industry 4.0 tech could solve the biggest risks in single use manufacturing facilities
April 16 by Pharma IQBilly Sisk of Rockwell Automation shares how Industry 4.0 could transform one of the biggest risks in single use; human error
Predictive Toxicology: Stem Cell Characterization Must Mature
March 17 by Pharma IQIn this interview, Phillip Hewitt, Head of Early Investigative Toxicology at Merck KGaA analyzes new innovations in predictive toxicology
First Biopharma Product Launch in Europe: What it Takes to Succeed
March 12 by L.E.K. ConsultingL.E.K. Consulting share the five key success factors needed for a biopharma launch
Life Sciences Manufacturing and Quality: The New Path to Performance
September 11 by Dan JacobAfter surveying over 1200 life science leaders, this research captures the shared role of quality and manufacturing across enterprise and operational domains in medicine production.
Standardisation within Single Use Systems An Inevitability, But Does It Have To Be Painful?
December 08 by Pharmaceuticals & Biotechnology EditorA dominating focus of today’s single use systems in biomanufacturing is the road towards standardisation between equipment suppliers. The absence of standardisation between single use system sup...
Investment Trends In Single Use Systems
November 24 by Pharmaceuticals & Biotechnology EditorAs the biopharmaceutical industry's focus moves from a blockbuster sales model to more targeted therapeutics, the need to avoid costly investments in sizable stainless steel equipment is increasing.Th...
Data Challenges in Biologics Development
November 05 by Pharmaceuticals & Biotechnology EditorThis paper explores how a single, enterprise data-management platform can improve biologics development lifecycles. The paper examines the challenges faced by biopharmaceutical professionals in thei...
Creating Effective Leachables and Extractables Testing: Whose Responsibility Is It?
April 20 by Eric LangerThe problem of leachables and extractables (L&E) in single-use devices continues to hound both suppliers and end-users, and remains one of the more challenging issues inhibiting regulatory accep...
Disposables Solutions 2015
February 09 by Tony HitchcockWith this year’s Disposables Solutions meeting in Munich rapidly approaching I will focus this blog on some of the issues which I hope will be covered in presentations and discussions. Looki...
Standardized Extractables Testing Protocol for Single-Use Systems in Biomanufacturing
December 16 by Pharmaceuticals & Biotechnology EditorThis article presents a consensus standardized extractables testing protocol for single-use systems in biomanufacturing. [inlinead] Have Your Say Rate this featu...
Under the Microscope: Extractables and Leachables in Single Use Systems
November 27 by Pharmaceuticals & Biotechnology EditorWith the release of the PDA Technical report 66 in mind, the adoption of single use systems has been again moved to the top of discussions in biomanufacturing and extractables and leachables is prov...