Resources
ICQ Blog
Executive Briefs
A CQV Checklist for Gene Therapy Facilities
/in Executive Briefs /by jlerman@coldspringdesign.comAs more cell and gene therapies receive approval, the commercial demand for these groundbreaking medical treatments will increase rapidly.
White Papers
Data Integrity: How to Prevent a Significant Source of 483s and Warning Letters in Drugs, Devices, and Biologics
/in White Papers /by projects@coldspringdesign.com5 Practical Ways to Proactively Avoid Data Integrity Issues for Improved Quality
Medical Device Manufacturing & Supply Chain: ISO 13485, ISO 9001, or 21 CFR 820?
/in Blog /by Ashley Farley