USP Conducted a Training on “Assessment of Analytical Method Integrity in Pharmaceutical Laboratories”

USP Conducted a Training on “Assessment of Analytical Method Integrity in Pharmaceutical Laboratories”

On September 28, 2026, a practical training session was organized on the assessment of the integrity of analytical methods used in pharmaceutical laboratories.

The event was attended by specialists from the State Institution “Center for Good Practices”, State Institution “Pharm Service” under the Agency for the Development of the Medical and Pharmaceutical Industry, as well as the State Institution “Center for Pharmaceutical Product Safety” under the Ministry of Health of the Republic of Uzbekistan.

The main objective of the training was to develop knowledge and skills in assessing the reliability of analytical methods used in pharmaceutical laboratories to determine qualitative and quantitative indicators, particularly from the perspective of using reference standards.

This knowledge will have practical significance in conducting GMP inspections in the future, as well as in evaluating validation data for analytical methods included in registration dossiers.

In addition to theoretical knowledge, the training programme also included practical sessions. Participants reviewed approaches to assessing analytical methods using examples close to real-life situations.