Suppliers / Shandong Focusfreda Biotech

Shandong Focusfreda Biotech

China Updated 9 July 2026

Shandong Focusfreda Biotech is an API manufacturer based in China. It holds one active US drug master file and one valid CEP across a filed portfolio of 2 molecules.

1
active US DMFs
1
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Qufu, China Not on file

What they file, and where

Molecule Regulators Docs
Hyaluronic Acid US FDA 1
Sodium Hyaluronate EDQM 1

Also appears on these molecule pages

Hyaluronic Acid API

Questions about Shandong Focusfreda Biotech

Does Shandong Focusfreda Biotech hold a US DMF or a CEP?
Shandong Focusfreda Biotech holds 1 active US drug master file and 1 valid CEP. 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.
Where does Shandong Focusfreda Biotech manufacture?
1 registered site is on record, in China (Qufu). Every site is listed on this page with the register it came from.
What does Shandong Focusfreda Biotech make?
2 molecules are on record against Shandong Focusfreda Biotech, including Hyaluronic Acid and Sodium Hyaluronate. Each links through to that molecule's full manufacturer list.

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.

Checking Shandong Focusfreda Biotech?

Ask Fred what the record holds on Shandong Focusfreda Biotech, including filings and inspection history.

Chat with Fred, your AI analyst
Opens WhatsApp. Free to start.

Comparable suppliers

Bloomage Biotechnology shares 1 molecule Shandong Topscience Biotech shares 1 molecule Htl shares 1 molecule Contipro shares 1 molecule AMHWA Biopharm Co.,Ltd shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability