Laboratorium Dr. Seeger

Chem.- Pharm. Laboratorium Dr. Seeger GmbH has a manufacturing authorisation in accordance with § 13 of the AMG [Drug Law]. This means that we analyse every single batch of our pharmaceutical starting materials, conducting all individual tests required by international pharmacopoeias such as Ph. Eur., USP and JP and issue certificates of analyses in accordance with WHO-GMP 17.17 and DIN EN 10204 requirements.
 
This is how the laboratory provides comprehensive documentation and thereby contributes to the smooth and complete exchange of data and know-how.
 
The result is (practically) unique: enclosed with every Hedinger delivery of starting materials is a certificate stating the batch number with all the relevant analytical data, something that many pharmaceutical manufacturers all over the world even include in their incoming control documentation.