Facilities
You are here:
Quality Assurance
R&D and Pilot Plant
Reliable Manufacturing
Quality Assurance
- Quality Management Systems in R&D as well as Manufacturing Facility in compliance to Domestic and International regulatory standards.
- Developmental Quality Assurance (DQA) and Quality assurance (QA) with dedicated team ensures all the activities are performed as per approved written procedures.
- Chromatographic instruments like HPLC’s and GC’s are installed with Open Lab CDS – 2.5+ version, are connected to the Server
- Non-chromatographic instruments like Particle Size Analyzer, Stability Chambers, UV spectrophotometer, FT-IR are connected to the server through qualified software’s,
- Qualified software’s are used for 21 CFR Part 11compliance.
- Documents generated at R&D and Manufacturing Facility shall be reviewed and authorized by respective QA teams for integrity, accuracy and proficiency before sharing documents to internal Regulatory Team or Customers.
- Provide periodical training and evaluation to all employees on cGMP and other behavior based aspects to maintain high degree of Integrity.
- Efficient Document Archival and Retrieval system and procedures for easy and quick access.
- Adherence to Statutory requirements and stringent Safety Health and Environment measures.
R&D and Pilot Plant
As a science-led pharmaceutical company, we invest in cutting-edge research to develop new cures for challenging diseases.
We are focused on undertaking dedicated R&D in areas with significant demand. Our research team of over 100 scientists constitutes a quarter of our total workforce. Our systematic approach to the selection of molecules, which involves evaluation of technical, and commercial feasibility data, and customer feedback helps us generate a good return on our research spending. Team has the history of commercializing 1000+ products.
Reliable Manufacturing
Built to world-class standards, our manufacturing facilities enable us to produce high-quality and affordable medicines.