Suppliers / Tillotts Pharma

Tillotts Pharma

Switzerland 293 employees Updated 9 July 2026

Tillotts Pharma is a finished-dose manufacturer based in Switzerland. It appears in 138 regulatory filings across 12 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, Health Canada and SWISSMEDIC (CH). Its GMP standing is certified by EMA and ZLG (DE).

0
active US DMFs
0
valid CEPs
4
registered plants
138
filings across 12 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Rheinfelden, United Arab Emirates Not on file
Ziefen, Switzerland Not on file
Rheinfelden, Switzerland Not on file
Rheinfelden (Baden), Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 24 4
Health Canada 21 None
SWISSMEDIC (CH) 18 None
MPA (SE) 12 None
DMP (NO) 11 None
INFARMED (PT) 10 None
ZLG (DE) None 4

Questions about Tillotts Pharma

Does Tillotts Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Tillotts Pharma. It does have 138 filings with 12 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Tillotts Pharma manufacture?
4 registered sites are on record, in United Arab Emirates, Switzerland and Germany (Rheinfelden, Ziefen and Rheinfelden (baden) among others). Every site is listed on this page with the register it came from.
Which regulators recognise Tillotts Pharma's GMP?
Current GMP certificates are on record from EMA and ZLG (DE). 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