Dr. Reddy's API Manufacturing Capabilities:
Dr. Reddy’s manufactures over 250+ APIs across India, Mexico, and the UK, with eight USFDA-inspected cGMP facilities that comply with ICH Q7 guidelines and are regularly audited by global regulators. With 40+ years of expertise, the company specializes in complex APIs such as steroids, peptides, long-chain molecules, and HPAPIs, supported by robust R&D and worldwide commercialization capabilities.
Focused on becoming the leading global API company, Dr. Reddy’s emphasizes innovation, a strong global footprint, and exceptional customer service. With multi-sourced KSMs, stringent quality standards, timely deliveries, and capacity expansion, the company ensures a reliable, sustainable supply chain, combining scientific expertise, compliance, and sustainability to be a trusted API partner.
API Manufacturing Capability
40+ years of expertise
Leading supplier of APIs for more than 40 years Leading supplier of APIs for more than 40 years Leading supplier of APIs for more than 40 years.
Eight manufacturing facilities
We have eight commercial USFDA inspected API pharma plants/production units, of which six are in India and one in Mexico and the UK.
Manufacturing Capacity
Sufficient manufacturing capacity and flexible batch sizes enable fast turnaround times, supported by backward integration and a resilient supply chain to ensure consistent, uninterrupted delivery.
Safety and Compliance
All our plants are operated in accordance with cGMP (ICH Q7a) and are regularly inspected/audited by international authorities and agencies.
Manufacturing Locations
Quality Control Policies
A key component in quality control in pharmaceutical industry is helping customers by providing a quality product. We achieve this by ensuring that all our facilities operate efficiently and to the latest quality, safety, and productivity standards.
At Dr. Reddy’s, quality control is central to our commitment to delivering safe, high-quality APIs. Our facilities operate under cGMP (ICH Q7) standards, ensuring global regulatory compliance and consistent product performance.
Advanced Analytical & Process Excellence
- Scalable manufacturing for consistent quality
- Robust analytical methods to eliminate nitrosamine and azido impurities
- Comprehensive impurity profiling , characterization, and control
- Use of advanced techniques to define chemical and physical attributes
- Efficient operations aligned with the latest quality, safety, and productivity standards
Related Pages
R & D
Customer Service
