Driven by Research, Defined by Quality.
The Pillar of Quality Control and Compliance
At DR R.K Pharmaceuticals, R&D is the engine of our proven excellence. Our dedicated facilities and expert teams ensure that every formulation we offer meets the highest global regulatory standards, including **WHO-GMP** (Good Manufacturing Practices) and **GLP** (Good Laboratory Practices).
Our Quality Assurance (QA) and Quality Control (QC) systems are integrated at every stage, from meticulous raw material sourcing to final batch release, guaranteeing safety, purity, and efficacy for all 300+ products in our portfolio.
- Regulatory Audits: Continuous internal and external audits to maintain compliance status.
- Advanced Testing: Use of modern analytical instruments for purity and stability testing.
- Documentation: Meticulous batch record keeping and transparent documentation for every product.
Core Areas of Research and Development
We focus our research efforts strategically to ensure a competitive and efficacious product line for our partners.
Novel Formulations
Developing innovative and stable drug delivery systems, particularly in pediatric and critical care segments.
Bioequivalence Testing
Rigorously testing our formulations to ensure equivalent safety and efficacy compared to branded drugs.
Stability Studies
Conducting accelerated and real-time stability studies to guarantee the declared shelf life of all products.