We have a setup for handling of external Audits with a good hands of experience team and having an experts of QP and WHO certified personnel
currently we will give a services of
- Facility Audit
- Product Dossier Review and Filling Gap Analysis
- Clinical Data Review and Report
- Vendor Audit of API & Excipient and Formulation sites of all Dosage Forms
- CMF Audits.
- R&D Facility Audit for Development and Validations.
- Review of ANDA’s Method Development and Method Validation.
- Conducting of gap Analysis for Existing Area to meet GMP Compliance across Major Global Requirements.