Analytical Services for Sterile Drug Products

At PCI, ensuring life-changing medicines reach those who need it most is our highest priority. As a truly integrated global CDMO, we are manufacturing, packaging and supply chain experts, harnessing our experience and expertise to deliver you a seamless solution with the ultimate aim of improving the lives of patients.


We have the capability to perform non-GMP and GMP photostability studies for drug substance and
finished product.

This includes:

  • Photostability protocol development utilizing ICH Q1B stability guidelines
  • Storing products in validated photostability chambers at the recommended light intensity
  • Time point management, time point testing, and data reporting with quality oversight
  • Final report

Our dedicated team of specialists will be happy to discuss any of your Analytical Services for Sterile Drug Products questions. Contact us on +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email

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Contact us. Get ready to experience true speed.

Rely on our analytical services for sterile drug products to expedite your drug product journey.

Spanning the cycle.A truly global proposition.

Always growing, we are driving development and connecting commercialization, and with 4300 people in 30 global GMP facilities, we are always close.