Suppliers / Bell, Sons & Co (Druggists)

Bell, Sons & Co (Druggists)

United Kingdom Updated 9 July 2026

Bell, Sons & Co (Druggists) is a finished-dose manufacturer based in United Kingdom. It appears in 227 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, FDA (GH) and EDE (AE). Its GMP standing is certified by MHRA (UK) and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
2
registered plants
227
filings across 4 regulators

Registered plants

Site FDA FEI
Merseyside, United Arab Emirates Not on file
SOUTHPORT, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 151 None
FDA (GH) 59 None
EDE (AE) 15 None
NAFDAC (NG) 2 1
MHRA (UK) None 2

Questions about Bell, Sons & Co (Druggists)

Does Bell, Sons & Co (Druggists) hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Bell, Sons & Co (Druggists). It does have 227 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Bell, Sons & Co (Druggists) manufacture?
2 registered sites are on record, in United Arab Emirates and United Kingdom (Merseyside and Southport). Every site is listed on this page with the register it came from.
Which regulators recognise Bell, Sons & Co (Druggists)'s GMP?
Current GMP certificates are on record from MHRA (UK) and NAFDAC (NG). 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