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 QICI
‘s expert consultants with average of 20 years in auditing
drugs, biotech, and device companies and clinical trials,
provide auditing services for:
- ISO 9001 and 13485 (audits are performed by
internationally registered auditors and lead auditors)
- QSR
- GMP, GLP, GDP, and GCP
- API and bulk pharmaceuticals CMOs
- Labeling and printing suppliers
- Contract fillers and packagers
- Contract testing laboratories
- Contract sterilizing companies
- Critical suppliers
- Mock FDA inspections
- Clinical investigational sites
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