For laboratories that operate within a quality management system, compliance to global standards such as ISO 9001, ISO 13485, ISO 17025, ISO 15189, GxP, and other country-specific regulations requires documented verification that instruments and equipment are installed and operating according to the manufacturer’s specifications for the design's intended use.

In this webinar, you’ll hear from compliance specialists at Thermo Fisher Scientific on the importance of complete qualification protocols and documentation, their value in process validation, and the importance of maintaining
a quality system.

Learning Objectives:

• Learn why qualifications (IQ/OQ/PQ) are important and when they are required
• Learn how instrument and equipment qualifications fit into process validation
• Learn what is included in qualifications from Unity™ Lab Services