Our Expertise
Manufacturing
- Shreeyan Medicare boasts world-class manufacturing facilities in Jammu, J&K, specializing in the production of tablets, and capsules.
- Committed to enhancing cost-efficiency and operational productivity, we leverage automation, advanced software, and resource planning strategies. Our relentless pursuit of improvement underscores our dedication to delivering high-quality pharmaceuticals.
- Shreeyan Medicare boasts world-class manufacturing facilities in Jammu, J&K, specializing in the production of tablets, and capsules.
- Our manufacturing facilities hold certifications for Good Manufacturing Practices (GMP) in accordance with WHO-GMP, EU-GMP, and various other international authorities. Additionally, we adhere to the ISO 9001:2015 quality management system standards.
- Committed to enhancing cost-efficiency and operational productivity, we leverage automation, advanced software, and resource planning strategies. Our relentless pursuit of improvement underscores our dedication to delivering high-quality pharmaceuticals.
- Excitingly, we have plans for a new facility in Jammu, which will expand our capabilities to include tablets, and capsules.
Research & Development
- At Shreeyan Medicare, we take pride in our dedicated Research and Development (R&D) laboratory, recognized by the Department of Scientific and Industrial Research (DSIR) for conducting in-house R&D initiatives.
- Our R&D laboratory is staffed by a skilled team of scientists and engineers, bringing extensive experience in formulations development and analytical method development. The facility is equipped with cutting-edge technology, including a suite of equipment for the development of solid oral and liquid dosage forms. This equipment encompasses rapid mixer granulator, fluid bed processor, compression machine, and auto coater.
- Furthermore, our analytical lab is equipped with state-of-the-art instruments such as high-pressure liquid chromatography, ultraviolet and dissolution apparatuses, Karl Fischer moisture analyzers, sonicators, disintegration testers, thermal stability units, and fume hoods. This advanced infrastructure underscores our commitment to innovation and ensuring the highest standards in pharmaceutical research and development.
Quality Assurance & Regulatory Affairs
- Significant investments in quality management systems and quality control laboratory information management system to support ‘electronic-based’ systems in manufacturing and quality controls as well as validation activities to enable to undertake data analytics and track product level information across the different facilities and teams.
- Modern Quality Control laboratory with gas Chromatography, HPLC, FTIR, Spectrophotometer
- Many of our key customers have audited and approved our facilities and manufacturing processes in the past, which ensures that the regulator and our customers are able to confirm the continuance of quality of our facility and processes.
- Newly equipped Control Sample Storage facility
- Active product registrations with international authorities with regular fresh registration applications in process with international authorities.
- Strong pipeline of process product dossiers for exports
- Strategy to expand our exports to developed markets with product registrations