Compliance and QA are integral to all R&D activities, ensuring adherence to cGMP, GLP, and global regulatory standards.
The organization follows well-defined SOPs across R&D, analytical, and quality activities to ensure uniform practices, proper documentation, and regulatory compliance (USFDA, MHRA, ROW).
The organization maintains a strong QA system to ensure regulatory compliance, controlled documentation, and effective change management across R&D and manufacturing.
The organization ensures data integrity and audit readiness through accurate documentation, regular audits, continuous monitoring, and ongoing cGMP/GLP training.
Medley House, D2,
M.I.D.C. Area,
Andheri (East),
Mumbai-400 093, INDIA