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Contract service providers must step up their game to stay competitive in increasingly complex bio/pharma market.
The need for preclinical testing expertise is growing as molecular complexity increases.
A look at the newest innovations offers a deeper understanding of affinity ligands and their role in the future of downstream processing.
August 01, 2016
Quality, innovation, and new approval pathways open drug development options for the Chinese market, including injectable contract manufacturing.
Bio/pharmaceutical contract service provides continue to invest in development, facility upgrades, technological advancement, and mergers and acquisitions.
New approaches add flexibility and reduce risk for contract development and manufacturing organizations (CDMOs) and their clients.
Planning ahead is key to enabling a continuous and secure supply chain that adapts to changes in market demand.
Now past the “wait-and-see” standoff, most pharmaceutical companies and their contract partners are considering long-term requirements, including distributors’ needs.
The author reviews some of the key considerations when selecting a vendor and crucial parameters that must be defined in the tech-transfer process to ensure the greatest chance of success.
Training and mock audits are the key to preventing data integrity issues with partners offshore, but the process must start at home. Compliance consultant John Avellanet shares best practices and ways to minimize costs.
July 20, 2016
The company plans to purchase and develop an 18-acre site in Des Plaines, Illinois.
July 12, 2016
EAG Laboratories announces new company identity and intent to expand testing, analysis, and characterization capabilities across multiple markets.
July 11, 2016
Patheon launches initial public offering to repay outstanding notes and expenses.