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Transo Pharm Handels GmbH

Not yet confirmed Manufacturing authorisation GMP certificate 22962 Siek · Schleswig-Holstein transopharm.de ↗

Profile

Transo-Pharm Handels-GmbH in Siek distributes pharmaceutical active ingredients worldwide, offering sourcing, qualification of active ingredient manufacturers, GMP-compliant storage and regulatory support such as the preparation of Drug Master Files.

Services

Evidenced: named on the company’s own website. Unclear: checked, nothing conclusive found.

ServiceStatusEvidenceQuote from the company’s website (German)
GMP audits and supplier qualification
Release and quality
Unclear

„Durchführung von Audits“

Source · 10 Nov 2026 ↗
QM and GMP consulting
Release and quality
Evidenced

„GMP-Beratung“

Source · 10 Nov 2026 ↗
Regulatory affairs
Regulatory and safety
Evidenced

„DMF-Erstellung und Registrierungen“

Source · 10 Nov 2026 ↗
GDP transport and storage
Logistics
Evidenced

„Lagerhaltung im eigenen GMP-Lager“

Source · 10 Nov 2026 ↗

Official credentials

Manufacturing authorisation

The competent authority of the federal state authorises the site to manufacture, test or import medicinal products (Section 13 of the German Medicinal Products Act, AMG). Without this authorisation it may not do so.

DE_SH_01_MIA_2026_0011

Siek

Source: EMA/EudraGMDP, reported by the competent state authority · as of 10 Nov 2026 ↗

GMP certificate

The authority has inspected the site and confirmed that it complies with Good Manufacturing Practice (GMP).

DE_SH_01_GMP_2026_0018

Siek

Source: EMA/EudraGMDP, reported by the competent state authority · as of 10 Nov 2026 ↗

Sites

Bueltbek 5
22962 Siek

Headquarters