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Testing services for the determination of inorganic components

OMPG's pharmaceutical testing services specialize in the determination of inorganic components of medicinal products, active ingredients and excipients. With our analytical expertise, we support you along the entire industrial process chain: from the start of your research and development projects to the testing of raw materials/ingredients and the release analysis of your end products.

We offer contract analyses and specific method developments in accordance with GMP for the determination of elemental impurities and other inorganic components in all phases of active ingredient and drug development as well as for the research, development and manufacture of drugs and generics.

As a GMP laboratory regularly monitored by the authorities, we guarantee you a high degree of precision and competence in the testing of pharmaceutical starting materials, intermediate products, semi-finished and finished goods.

Our current GMP certificate shows an overview of the methods which we are approved for as a testing laboratory within the meaning of § 14 (4) AMG. In addition, the compliance of our work with GMP requirements is confirmed by regular audits by pharmaceutical companies and the FDA.


Our services

Pharmaceutical tests

  • Determination of elements according to all common pharmacopoeias:
    • European Pharmacopoeia (Ph. Eur.)
    • U.S. Pharmacopeia (USP)
  • Analyses according to customer-specific test instructions
  • Development and validation of analytical methods for:
    • Content determination
    • Purity determination
    • Limit value and residue testing
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