GMP Laboratory Analyst Qualification

GMP Laboratory Analyst Certification

This practical two-day training course is designed to qualify analysts for proper and compliant work in Quality Control laboratories in the pharmaceutical and medical device industries.

The course focuses on the practical implementation of USP-NF and EP pharmacopoeias, understanding the principles behind analytical methods, and performing laboratory tests correctly and consistently.

Course Details

Duration: 2 days
Dates: 05.01.27 | 12.01.27
Hours: 09:30–16:00
Format: Frontal

What You Will Learn

• Identification tests and limit tests
• Titrations, including Karl Fischer
• Laboratory water testing, including pH, conductivity and TOC
• IR, FTIR, NIR and UV-Vis spectroscopy
• AA, AES and ICP techniques
• Separation methods, including TLC, HPLC, UPLC and GC

Participants will gain a consistent professional language for working with pharmacopoeias, improve the correct and repeatable execution of analytical test methods, and strengthen their readiness for audits and inspections.

Who Should Attend?

• Analysts working in the pharmaceutical and medical device industries
• QC and QA professionals
• Professionals seeking practical and precise qualification in performing analytical test methods in a GMP environment

Registration Information

The course is available as an in-house training program for company teams, on dates coordinated in advance.

Alternatively, participants may register for the waiting list for a future open course.

An open course will be scheduled subject to a minimum registration of six participants. Once a suitable group has been formed, registered participants will be contacted to confirm the course date and complete the registration process.

Registration for the waiting list does not constitute final confirmation that an open course will take place. The course date will be determined and communicated once the minimum number of participants has been reached.