Ensuring compliance and the safety of your products with our reliable biopharma and medical device microbiology testing services

Our state-of-the-art laboratories and experienced subject matter experts (SMEs) deliver precise, reliable results compliant to regulatory requirements.

Medical devices

Our microbiology testing solutions support a wide range of pharmaceutical products and medical devices, including:

  • Active pharmaceutical ingredients (APIs)
  • Capsules, tablets, pellets, and syrups
  • Creams, ointments, and gels
  • Injectable drugs
  • Medical devices, including inhalers, stents, implants, etc.

Regulatory compliance & testing standards

Our testing methodologies adhere to international regulatory and pharmacopeial standards, ensuring full compliance with:

  • United States Pharmacopeia (USP)
  • European Pharmacopeia (EP)
  • Japanese Pharmacopeia (JP)
  • Indian Pharmacopeia (IP)
  • British Pharmacopeia (BP)
  • ICH guidelines
  • ISO/NABL Standards
  • Client Specifications

Frequently asked questions (FAQ)

What is the turnaround time for microbiology testing?

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Turnaround time varies based on the type of test but typically ranges from a couple of days to a couple of weeks. Contact us to know timelines for your specific testing requirements.

Do you provide customised microbiology testing solutions?

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Yes, we offer customised testing solutions to meet client-specific needs, including method development, validation, and batch analysis.

How do you ensure regulatory compliance in microbiology testing?

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We strictly adhere to international standards such as USP, EP, JP, IP, BP, and ISO.

What industries can benefit from microbiology testing services?

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Our microbiology testing services cater to the pharmaceutical, and medical devices industries ensuring product safety and enabling compliance.

Can you help with method development and validation for new products?

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Yes, our expert team specialises in method development and validation for new products, ensuring accurate and reliable testing results.

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