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Sourcing and Distribution Analytical Services

Pharmaceutical analytical services that keep your sourced materials safe, compliant and ready to move.

Analytical support protecting your supply

Our specialised analytical expertise is integrated directly into our sourcing and distribution process. We ensure that every pharmaceutical ingredient we deliver to you is compliant, reliable and verified, allowing you to mitigate supply chain risk and maintain confidence in the quality you receive.

 

Our commitment to analytical excellence

Our state-of-the-art laboratories are led by highly trained professionals with deep, current expertise. All analyses can be performed in compliance with the necessary GMP, ICH and ISO standards to support full assurance across your supply chain.

Testing is carried out according to pharmacopoeial methods or tailored to your specific needs. To support validity, our analytical procedures are developed, optimised, verified for compendial use and validated for internal methods in line with ICH guidelines.

 

Specialised expertise for complex materials

Our analytical specialists bring extensive experience in small molecule analyses and maintain advanced capabilities for verifying and characterising complex large molecules including proteins, peptides, antibodies, bioconjugates, oligonucleotides and PROTACs.


Our Capabilities at a Glance

  • Identity testing, assay and related substances (HPLC or GC)
  • Chemical testing (pH, density, conductivity or optical rotation)
  • Residual solvents and water content
  • Impurity profiling and characterisation
  • Nitrosamine testing
  • Specialised techniques including HIC, SEC and high resolution MS
  • Particle size distribution
  • Excipient analysis
  • Leachables and extractables studies
  • Compatibility and in-use studies
  • Stability and solubility studies

Our latest news and insights

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Ofichem acquires Avivia B.V. to expand formulation development capabilities

09 Jul 25
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Pharmaceutical Dissolution Testing Theory

28 Nov 24
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Accelerating drug development using 505(b)(2) regulatory pathways

12 Mar 24
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