We develop formulations for Solids (Tablets, Powder for solution, Suspensions), Liquid orals, Sterile formulations, Inhalations for NDA & ANDA through quality policies.
Analytical development at KMS Pharma is integrated with product development and Quality assurance teams to ensure effective and accelerated product development.
KMS Pharma provides end to end support on technology transfer from the drug discovery stage to product development, to clinical trials, and finally to full-scale commercialization.
KMS Pharma has association with experienced Clinical Research Organizations (CRO) across India, explicitly concerning Bioequivalence & Bioavailability (BA/BE) Studies & Phase I-IV Clinical Trials.
KMS Pharma has a good understanding of the global regulatory requirements. The regulatory team is involved in all the stages of the drug development.