Search results for " process" in Articles / App Notes
Article
Innovation vs. Capacity: How CMOs Compete
Characteristics of capacity-driven CMOs include:
• Business strategy based on acquiring and/or maintaining capacity for routine manufacturing processes such as direct compression solid dose presen…
Article
A Q&A with Eric Langer: CMOs Embrace New Technology
… chromatography, single-use probes and sensors, disposable chromatography, instrumentation, upstream process development services, etc. In comparison, biopharmaceutical innovators sought improved ana…
Article
Maximize resin usage with continuous bioprocessing
Periodic counter-current chromatography (PCC) is a multi-step approach to maximize the chromatography resin capacity utilization and minimize process time. The technology employs three or more chromat…
Article
Vaccine Development Faces Urgency and Challenges
Scientific advances
To achieve these goals, scientists in academia, government, and industry are moving to tap new genomics technology to reduce the long R&D process and help modernize vaccine dev…
Article
A Q&A With Jeff Carter on Trends in Single-Use Technologies
This development will lead to the increasing availability of high quality single-use material information which, in turn, will provide greater technical insight to process performance. This will help …
Article
Innovative Therapies Require Modern Manufacturing Systems
At the same time, though, the development of such innovative and targeted therapies heightens the importance of establishing production systems and processes capable of fast scale-up of high-quality c…
Article
Framing Biopharma Success in 2016
… now prescribed as lower-cost generic drugs--has implications for drug development and manufacturing processes.
A market research study estimates that the global biosimilars/follow-on-biologics m…
Article
Automated harvesting and 2-step purification of unclarified mammalian cell-culture broths containing antibodies
The staggered parallel multi-step configuration of the system allows unattended processing of eight samples in less than 24 hours. The system was validated with a random panel of 45 whole-cell culture…
Article
Labeling of Biosimilars
Feb 01, 2015
By Sean Milmo
BioPharm International
The European Medicines Agency (EMA) has reached a key stage in the lengthy process of creating a regulatory framework for the development and…
Article
New Era for Generic Drugs
An unanticipated problem is that more than 1400 applications were filed this past year, many more than projected, making it even more necessary for OGD to implement a new review process that sets prio…