Equipment qualification is a critical step in ensuring that a product or service is provided accurately and consistently with regards to manufacturing and testing. The time-saving attribute of adding ...

It ensures that all processes and equipment affecting the quality, integrity, safety and efficacy of the pharmaceutical product are qualified and validated. All necessary activities and ...

Consistent practical methods for defining equipment qualification and testing requirements can improve subsea equipment reliability and facilitate project execution. ExxonMobil Development Co ...

Installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) are the three steps of equipment qualification. Although most drug companies either have a ...

For laboratories that operate within quality management systems for compliance with global standards such as ISO 9001, ISO 13485, ISO 17025, ISO 15189, GxP, etc. and other country-specific regulations ...

PORTLAND, Ore.--(BUSINESS WIRE)--NuScale Power Corporation (NuScale) and National Technical Systems (NTS) signed a Business Collaboration Agreement (BCA) to begin development of an Equipment ...

Incorporating facility/equipment qualification, process validation and validation of analytical methods for requirements in Europe, US and elsewhere, including ICH. This course is suitable for those ...

Aircell on Sunday said its Aircell Axxess communications system and Data Interface Unit (DIU) have received approval in SITA’s Validation, Assessment & Qualification (VAQ) program. As FANS over ...

For laboratories that operate within quality management systems for compliance with global standards such as ISO 9001, ISO 13485, ISO 17025, ISO 15189, GxP, etc. and other country-specific regulations ...