At Achyut, “Quality & Excellence” is part of each and every step. Planning focuses on all areas of operation comprising procurement of the raw materials, to synthesis, then Storage and precise delivery as per customer's requirements.
Achyuts’s Quality Assurance Department, constantly monitors and appraises the service as per SOP’s to ensure requirements for Quality are being satisfied.
Achyut conducts periodic self-assessments through a voluntary self-audit of its operations, in order to remain internationally competitive, and maintaining an effective Quality Management System.
Achyut embraces, a full-fledged Quality Control Laboratory, which follows and integrates up-to-date, contemporary, and high-tech testing equipment, in order to perform the stringent quality analytical tests
At Achyut, Document and Data are maintained to control all documents that form part of its management system, internally generated or from external sources, including SOP’s with master and Controlled Copy, Test and Calibration Records, Soft copy of Data on Server.
Quality Policy
To develop quality, safe and efficacious Pharmaceutical Standards, Drug Materials, Drug Products, Developing Chemical Research, Giving Quality Analytical Testing services by continuous monitoring of quality systems. Uphold to strict quality principles and meeting customer’s expectations by involving all the Employees of the Organization.
To maintain quality system as per the requirements of the International Standard.
To maintain quality system as per the requirements of the International Standard.
Quality Management System
We at Achyut have a full Quality Management System to control the Quality from concept to Commercialization.
Quality and Purity Assessment
At Achyut, we Qualify the Synthesized compounds for Identification / structure elucidation and Qualification by HNMR and 13C-NMR, MASS, IR Spectroscopy, CHNS and Purity by HPLC/GC/Chemical Analysis. Purity/Potency is defined by Mass Balance Method using Chromatographic purity and TGA Data, For Volatile Compounds Ash Content is performed.
After Qualification, product is sent into Global Warehouse. Inventory Team Checks the product for Quality, from Description to all Characterized Data and approves the qualification Report with interpretation of all Data.
Once the Material is Qualified and Approved, it is taken into Approved Area and made available for Dispatching.
Before Dispatch, the material is again Reviewed and Checked by Dispatch QA. Once the Dispatch QA approves the Quality and Documents as per Specification, it is ready to Dispatch.
