At Bright Star Trading
Pharmaceuticals companies are responsible for developing high quality assurance practice. A commitment to high- quality result is of utmost importance to operations of the successful pharmaceutical company. Quality is the essence of our business. Quality is not built up overnight. It has to be nurtured since inception and must remain in focus throughout.
At bright star trading, we believe in continuous quality assurance with in-house quality checks right from raw material testing at receipt stage through in - process checks to finished product testing. Hence our quality process begins with vendor selection. The receipt of materials, its storage and dispensing are done as per SOPs.
The entire manufacturing operation is carried out as per GMP / WHO by qualified pharmacists and trained operators as per validated process under direct supervision of senior pharmacists. Products are checked by IPQC and QC during the entire manufacturing process as per the SOP's. Finished products are sent into the market only on approval of QA department. Samples of every batch are retained for tests, while the product is in the market for the entire period of its shelf-life.
Production-integrated computer systems guide, control and document every step of the production process operated by trained staff.
Every finished product is manufactured and tested for compliance with relevant legal requirements (EU-GMP guidelines, Marketing Authorizations) and is released for sale by our Qualified Person.
The specifications and test methods according Marketing Authorization comply with the requirements of the European Pharmacopoeia and USP (American Pharmacopoeia).
All tablets are additionally subjected to dissolution tests, to ensure perfect active ingredient absorption.
Our laboratory is state-of-the-art. Over 25 HPLC units are available for analysis of the final products.
Curious to learn more? Give us a call and our knowledgeable team will be delighted to assist you!