Regulations and trends in pharmaceutical analysis and quality control are constantly evolving. It is critical to stay up-to-date on new analysis and testing techniques, trends, and regulatory changes to bring to market the highest quality pharmaceutical products in the most efficient manner.
In these articles MilliporeSigma’s technical experts provide the insight, technologies and solutions to make the drug development process as effective and streamlined as possible.
QC Corner: Practical Tips for Monomer/Aggregate and Fragment Content Monitoring of mAbs and ADCs
Product characterization is the essential foundation for successful biological drug development.Read More
QC Corner: Upholding Biosafety Standards Despite the Acute Need for a SARS-CoV-2 Vaccine
Viral vaccines were the first pharmaceuticals manufactured using living cells, revolutionizing the ... Read More
QC Corner: Single-Use Systems Underline the Rising Significance of Extractables and Leachables Studies
Examining extractables and leachables is an important safety issue as these substances can adversely... Read More
Why analyte binding to syringe filters must be studied during filter validation for QC testing
Many pharmaceutical QC tests such as dissolution testing, content uniformity, assay, and blend ... Read More
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