Getz Pharma Research initiates each drug development program with major consideration for implementing the most effective regulatory strategy to cost-effectively achieve near and long-term goals. We believe potential issues addressed early will accelerate overall development time.

GPR offers customers a fully integrated and seamless dosage form development program generally includes API characterization, patent landscaping, pre-formulation studies, excipient- compatibility studies, product-pack integrity studies, analytical methods development and validation, development of non-infringing formulation, composition and process optimization, stability studies, scale-up and process validation, manufacture of registration/ submission batches, assist client in preparation of the ICH Module P3 / Chemistry, Manufacturing and Controls (CMC) section and SUPAC support.

GPR also offers niche services viz. design and implementation of quality-by-design (QbD) to new product development and operations.