Suppliers / Bspg Laboratories

Bspg Laboratories

United Kingdom 21 employees Updated 9 July 2026

Bspg Laboratories is an API manufacturer based in United Kingdom. It holds one valid CEP. Its GMP standing is certified by MHRA (UK).

0
active US DMFs
1
valid CEPs
2
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Sandwich, United Kingdom Not on file
United Kingdom, United Kingdom 3012926417

What they file, and where

Molecule Regulators Docs
Cannabidiol EDQM 1

Also appears on these molecule pages

Cannabidiol API

Filings and GMP by regulator

Regulator Filings GMP certificates
MHRA (UK) None 4

Questions about Bspg Laboratories

Does Bspg Laboratories hold a US DMF or a CEP?
Bspg Laboratories holds 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.
Is Bspg Laboratories FDA-registered?
One site operated by Bspg Laboratories 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.
Where does Bspg Laboratories manufacture?
2 registered sites are on record, in United Kingdom (Sandwich and United Kingdom). Every site is listed on this page with the register it came from.
What does Bspg Laboratories make?
1 molecule is on record against Bspg Laboratories, including Cannabidiol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Bspg Laboratories's GMP?
Current GMP certificates are on record from MHRA (UK). 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.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates