Does Shandong Jincheng Bio-pharmaceutical Co.,Ltd hold a US DMF or a CEP?
Shandong Jincheng Bio-pharmaceutical Co.,Ltd holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Shandong Jincheng Bio-pharmaceutical Co.,Ltd FDA-registered?
One site operated by Shandong Jincheng Bio-pharmaceutical Co.,Ltd carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Shandong Jincheng Bio-pharmaceutical Co.,Ltd's last inspection go?
The most recent inspection on record closed on 15 November 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Shandong Jincheng Bio-pharmaceutical Co.,Ltd manufacture?
1 registered site is on record, in China (China). Every site is listed on this page with the register it came from.
What does Shandong Jincheng Bio-pharmaceutical Co.,Ltd make?
1 molecule is on record against Shandong Jincheng Bio-pharmaceutical Co.,Ltd, including Glutathione. Each links through to that molecule's full manufacturer list.
Which regulators recognise Shandong Jincheng Bio-pharmaceutical Co.,Ltd's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.
Answered from this company's own record. Where a register holds nothing, the question
is not asked rather than answered with a zero.
How we count our figures.