FDA sent a warning letter , dated Nov. 30, 2018, to Cao Medical Equipment Co., Ltd. detailing current good manufacturing practice (CGMP) violations agency inspectors observed during an inspection of the company s Langfang Industrial Zone, Langfang, Hebei facility, which was performed from JulOriginal Article
You may also like
Pharmaceutical Sales Customer Engagement –...
AstraZeneca’s Polyneuropathy Treatment Recommended...
Designing a Strategic Roadmap for Seamless Product...
AAPS PharmSci 360: LBFs and Tackling Oral Biologic...
CHMP Gives Positive Opinion to Novo Nordisk Hemophilia...
GSK, Cambridge to Partner on R&D for Kidney and...
About the author
David Miller
a pharmacist, a tech enthusiastic, who explored the Internet to gather all latest information pharma, biotech, healthcare and other related industries.