Clinical Trials Day

Validation

Sanjeevani provides sustained compliance and quality management Validation services by supplying a centralized location that efficiently and effectively controls documentation and GxP processes. Sanjeevani’s quality management Validation services has been specifically formulated to serve the compliance needs of regulated companies in life science industries such as:

Pharmaceutical
Medical Devices
Biotechnology
Blood/Tissue
Laboratories
Contract Organizations

Sanjeevani has developed state-of-the-art location for document control and quality management services that are 100% compliant with Part 11 regulations. Sanjeevani can establish and execute programs covering all phases of validation for all products, equipment, and processes. We develop process and/or equipment protocols for formulation, labeling, filling, and packaging for all products, including all support systems. We develop cleaning validation protocols, cleaning assessments, and provide relevant information for cleaning method development.

Sanjeevani can Author / revise validation standard operating procedures and validation master plans as needed. Sanjeevani can oversee and coordinate validation activities for process, equipment, instrument and cleaning validation studies. Sanjeevani assures full compliance with cGMP’s and other related requirements. We also collect, collate and analyze validation data and prepare final validation reports for approval. Sanjeevani reviews data, validation protocols, and reports.