Quality Analysis

Quality Analysis

Good Manufacturing Practice is an integral component of medicine manufacture. We at Agatsya Aushadh ardendtly follow these fundamentals to ensure good quality products. Stringent checks are conducted right from the receival of the raw materials , its identification and manufacturing upto the finished products. The testing and standardization of the formulations using scientific methodologies adds to the quality and authenticity of the product.

We have also collaborated with the AYUSH approved laboratories for the further analysis of our Raw materials and finished products. Testing specifications and Protocols are followed as per the guidelines provided in the Ayurvedic Pharmacopoeia of India. Ethically sourced raw materials received are identified, on approval are proceeded for manufacturing, the ones not approved are rejected. The evaluation of organoleptic characteristics of the finished products are conducted by the QA department. Various tools and techniques are implied to verify and ensure the required quality to be incorporated into the medicines. The finished products are tested according to the standard parameters and analytical procedures prescribed in the Pharmacopoeial Standards for Ayurvedic Formulations by the Government of India. Each batch preparation is documented by maintaining Batch Manufacturing Records that includes the Quality certificate.

With an objective to yield safe and effective products of superlative quality, We have implemented the Good Manufacturing Practices and Standard Operating Procedures following all the essential guidelines.