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Your Partner for Quality Control

WESSLING is your competent partner with long-term experience in pharmaceutical analysis, for the production as well as the import and export of pharmaceutical products.

Under the GMP conditions, we test pharmaceutical products: APIs and intermediate products as well as Finished Drug Products according to Ph. Eur., USP, BP and others. Our laboratories are registered testing laboratories according to the AMG and are subject to permanent supervision by the national authorities. In addition, all WESSLING laboratories are accredited according to DIN EN ISO 17025.

We offer you a wide spectrum of examinations for your product test like pharmaceutical tests, physical tests and pharmaceutical tests as well as microbiological tests and special tests.

Method validations are carried out according to ICH guidelines and are elaborated on your demands.

Our success is not only based on our modern technology and our strict quality mangement system; we owe it moreover to our experts, who have a profound knowledge of the relevant markets as well as the corresponding legislation.
Main focuses:

Qualifications

Special tests

  • Pesticide residues
  • Content of residual solvents
  • Specific impurities
  • Heavy metals of ICP-OES, MS
  • Stability tests
  • Biological equivalence
  • Endotoxin
  • Aflatoxin
  • more...

Service spotlights

  • Microbiological tests
  • According to Ph. Eur.
  • According to:
    DAB
    HAB
    USP
    BP
    Chinese Pharmacopoeia
  • Batch Release tests
  • Method development
  • more...