Shilpa Medicare Limited
Non-GMP Services

Non-GMP Services

Your Partner in Pharmaceutical Excellence

Learn more about our non-gmp chemical development services services and capabilities.

Overview

Lab development, POC, Demo batches cum scale up activities from 1 Kg to 1 MT scale

We offer Intermediates/API products under GMP (Good Manufacturing Practice) standards and requirements, we also provide vide range of products and related analytical services for non-GMP/GLP grade products.

Our non-GMP services are available for a broad range of customers. We can accommodate a variety of research scales and also offer additional analytical and storage services.

Our non-GMP development services offer you greater flexibility and speed. With a state-of-the-art facility, we are able to focus on lab-scale experiments with batch sizes ranging from mg to kg. Our strength is our non-GMP and GMP facilities residing at the same place, so that we can provide a seam quality between the development and GMP phases.

Why Choose Our Non-GMP Services?

Fast turnaround times, competitive pricing, and experienced team of chemists with expertise in complex chemistry.

Early-Stage Development Scope

Our non-GMP chemical development supports the earliest stages of the CDMO lifecycle, including:

  • •Route scouting & feasibility — alternative synthetic route design, cost-of-goods modelling, raw material sourcing assessment, intellectual property landscape review
  • •Process research & development — reaction optimisation, catalyst and reagent screening, asymmetric and chiral synthesis, solvent selection, yield improvement

Part of Shilpa's Raichur CDMO Platform

Non-GMP development is carried out at Shilpa Medicare's Raichur, Karnataka facilities, part of a small-molecule CDMO platform spanning approximately 1,160 KL of reactor capacity across 21 blocks, including nine dedicated high-containment blocks engineered to OEL-4.