We at Denisco rely on the preparation, review, and approval of SOPs, protocols, and reports for producing a perfectly customized product. Our validation team collect necessary information about all the products and develop a well-organized set of documents, which are in accordance with the ISO 9001 guidelines. Rejecting the raw materials when the content is exposed and identifying the proper storage location for the finished product is the key to our remarkable products.

Our vendors and contractors are well-qualified to ensure the quality of materials and components are in accordance with the regulatory guidelines. Additionally, the leading Computer system validation (21 CFR parts 11), process validation, cleaning validation, and analytical method transfers & process technology plays a key role in the process of product validation.

Training and development of the staff is done in accordance with the trend of pharmaceutical products. Ensuring GMP compliance of the facility is the basic framework we do at Denisco.