Method Development and Validation

Since our founding in 1994, PMRS has validated hundreds of analytical methods in various product formulations. From tablets and capsules to creams and extrusions, we will work closely with you to achieve superior quality for the lowest cost.

Our methods are:

• Developed and validated according to either specific client requirements or our own extensive Standard Operating Procedure.
• Validated in compliance with FDA and ICH guidelines.

We also provide development of residual cleaning verification methods:

• We develop and optimize residual cleaning verification methods for all active pharmaceutical ingredients and cleaning agents.
• We analyze and verify the cleanliness of all major equipment after every manufacturing campaign.
• We evaluate active and cleaning agent cleanliness to ensure the highest quality and purity for all products.