Document Verification

Thorough physical inspection of pharmaceutical shipments to verify compliance with regulatory standards and specifications.

Manufacturing Records Review

Detailed examination of manufacturing records to ensure adherence to Good Manufacturing Practices (GMP).

Quality Assessment

Comprehensive evaluation of product quality, including visual inspection, packaging integrity, and labeling accuracy.

Sampling and testing

Sampling of pharmaceutical products followed by rigorous testing and analysis in accredited laboratories to assess safety, efficacy, and quality.

Document verification

valid manufacturing license, Good Manufacturing Practices (GMP) certificate, Certificate of Analysis, import license, product registration certificate

Physical inspection prior to shipment

Verify packaging, damage, verify if product is manufactured in the same site as the registered site.

Testing and analysis in accredited laboratories

Ensure product meets quality specification Certification – required for customs clearance in the country of import

Issuance of Clean Report

This document serves as proof that the goods have been inspected and found to comply with applicable standards and regulations. It may be required by customs authorities or other regulatory bodies as part of the import/export clearance process.