GMP Analysis | NMI TT Pharmaservices

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Bioanalytics

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NMI-TT Contact Person

Dr. Ute Metzger

+49 7121 51530 849




GMP Analysis

GMP compliant testing procedures are provided for new biomaterials, excipients and active substances, for pharma quality control.

    The following techniques are established:
  • Rheometry (oscillation or rotation mode)
  • FTIR (transmission or reflexion mode)
  • HPLC-MS, GC, and SEC
  • UV-VIS spectroscopy
  • ELISAs

The testing laboratory holds a pharmaceutical manufacturing licence according to German drug law (§13 AMG). A GMP certificate has been issued by the local competent authority.

We offer our services to pharmaceutical companies as well as academic institutions developing therapies for clinical applications. Our main focus is on advanced therapy medicinal products (ATMP).

    We analyse:
  • Identity
  • Drug content, purity and impurities
  • Drug release
  • Residual solvents
  • Monomer content
  • Endotoxicity/pyrogens (LAL & MAT)

 

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NMI TT is a subsidiary of NMI