An on-site GMP audit will identify any GMP non-compliance (gap analysis) and recommend how they should be addressed. This is by far the best way to ensure that a company is GMP compliant and regulatory audit ready.
- We facilitate GMP auditing for equipment, facilities, utilities, processes and process installations.
- We facilitate onsite factory audits to assure that pharmaceutical intermediates are produced consistently and are strictly controlled to meet both national and international standards appropriate for their intended use. We assist our sources to ensure that related -regulatory requirements (FDA) are met.