Operating rigorous Quality Management Systems (QMS) compliant with WHO-GMP, cGMP, and international pharmacopeias.
Independent analytical testing of incoming raw materials, packaging components, in-process samples, and finished batches.
Overseeing cGMP compliance, validation protocols, change control, risk assessments, and batch record reviews.
Walk-in stability chambers simulating Zone I to Zone IVb climatic conditions for real-time and accelerated shelf life validation.