Introduction

A Certificate of Analysis is an official document that is issued by Quality Assurance Department that confirms that a product has met its predetermined product release specifications and quality. At Taj Pharmaceuticals, our QA teams issues all products COA before batch release of any pharmaceuticals product to the market.

COAs assist our company in avoiding costly returns, replacements, or customer complaints. This document is primary document which helps to follow pre-set product specifications and narrates all the standard testings that shall be conducted on the material in-ward and finished product outward movement from the Taj Pharma manufacturing plants.

Purpose of COA:

Reporting analytical results for a particular batch of:

  1. Raw Material
  2. Component
  3. API
  4. Finished product

Benefit of COA:

  1. Suppliers/Vendors are sending us high quality product that meets our strict production requirements
  2. Sending customers / exporting finished pharmaceuticals products that meets USP/BP/IP/IHS and customer specification requirements.

Format of COA

Certificate of Analysis

(Form 39, Rule 150 E (F) THE DRUG AND COSMETIC ACT, 1940 AND THE RULES THERE UNDER)

Finished Product Analytical Report