How To Apostille, Authenticate & Legalize a Certificate of Pharmaceutical Product

The "Certificate of Pharmaceutical Product (CPP)" is an internationally recognized document used for the export and import of pharmaceutical products.
This document contains information about pharmaceutical products that comply with international pharmaceutical regulations and standards, 

and it is issued by the government authorities or regulatory bodies of the exporting country.

The purpose of the CPP is to provide the necessary information for the imported pharmaceutical product to be eligible for approval in the importing country.

The CPP typically includes the following information: 

1. Manufacturer Information: Details about the company that produced the pharmaceutical product, including their address.

2. Product Information: Commercial name, generic name, product code, and other identifying details of the pharmaceutical product.

3. Specifications and Ingredients: Information about the ingredients and their quantities in the pharmaceutical product, as well as its formulation. 

4. Quality-related Information: Details about the manufacturing process, quality control systems, safety assessment, and related information. 

5. Registration or Approval Information: Information about the pharmaceutical product's registration or approval in the exporting country.

6. Storage and Transportation Conditions: Information about the appropriate storage and transportation conditions for the pharmaceutical product.

The CPP is typically prepared according to internationally standardized formats and must be endorsed by the regulatory authorities of the importing country. 

In the importing country, the document is reviewed to ensure that the pharmaceutical product is safe and compliant