MA24 understands the demands of working in a highly regulated and complex market sector when it comes to commissioning qualification and validation. We abide by the Current Good Manufacturing Practice (cGMP) and comply with Medicines and Healthcare Products Regulatory Agency (MHRA) and Food and Drug Administration (FDA) regulations where validation and quality assurance drive best practice.
Our commissioning, qualification and validation process includes a structured approach, which is built in from the start and flows throughout a project from design, delivery, installation, commissioning, validation, and handover of a facility. Our entire team understands the CQV needs and integrates it into the way they work. We cover DQ, FAT, SAT, Commissioning Reports, IQ, OQ, PQ.
Our four-stage validation master plan has been developed to ensure project success:
Validation:
Impact Assessment:
Validation Controls:
Validation Execution:
Telephone:
+44 (0) 1249 470950
General Enquiries:
sales@ma24.co.uk
Accounts Enquiries:
accounts@ma24.co.uk
Telephone:
+32 16 79 77 00
General Enquiries:
info@ma24.be
Accounts Enquiries:
accounts@ma24.be