IT Quality Management (ITQM)
Since 1992, CATADIA has dealt closely with the requirements for the regulated pharmaceuticals industry as laid down by Good Manufacturing Practise (GMP).
Our areas of expertise include:
- Planning and developing IT QM concepts and systems
- Conducting GAMP 5 audits (customer, supplier)
- Computer System Validation (CSV) in accordance with GAMP 5
- IT system management SOP development (in compliance with ITIL)
We can rely on many years of interdisciplinary experience in an international context as well as successful collaboration with multinational IT companies and partners in a wide range of industries. Our many reference projects demonstrate our experience.
Please contact us. We look forward to providing your company with our services too.