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Outsourcing is taking on a greater role in the biopharmaceutical manufacturing industry
British Library Online Contents | 2014| -
The ability to define a scientifically justified and statistically sound sampling procedure is a fundamental skill
British Library Online Contents | 2014| -
Advances in Linker Technology: Improving the Safety and Efficacy of Antibody Drug Conjugates
British Library Online Contents | 2014| -
FDA draft guidances seek to maintain accurate drug information in new media
British Library Online Contents | 2014| -
Progress is being made in the development of harmonized best practices for single-use systems
British Library Online Contents | 2014| -
Advances in UPLC Techniques and Column Chemistry Aid the Confirmation of Biosimilarity
British Library Online Contents | 2014| -
Performing degradation studies is the best strategy to evaluate toxicity risk
British Library Online Contents | 2014| -
Manufacturers are taking measures to comply with new package safety rules
British Library Online Contents | 2014| -
Troubleshooting Developing and maintaining a current master plan are crucial to manage cleaning validation
British Library Online Contents | 2014| -
Industry associations play a strong role in helping the pharmaceutical industry meet challenges
British Library Online Contents | 2014| -
Control Strategies for Synthetic Therapeutic Peptide APIs Part III: Manufacturing Process Considerations
British Library Online Contents | 2014| -
Changes are needed to maintain US biopharma innovation leadership
British Library Online Contents | 2014| -
The trend of exits from the CMO industry looks to be gaining momentum
British Library Online Contents | 2014| -
Review of Orthogonal Methods to SEC for Quantitation and Characterization of Protein Aggregates
British Library Online Contents | 2014| -
Manufacturers face regulatory overhaul, while brand-generic debates escalate over biosimilars and labeling changes
British Library Online Contents | 2014|
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