We Synthesis Innovative and Reliable Products
SRINAG PHARMA established in the year 2017 is one of the leading pellets manufacturing suppliers in India with state-of-the-art manufacturing and R & D facilities located at Hyderabad, Telangana, India.
With the world class semi finished formulations manufacturing facility for Pellets, Micro-Pellets and Granules with GMP approvals, the Company supplies various Products to Customer across the Globe. It has the best Operational Facilities, Scientific excellence & Innovative technologies to manufacture the quality products that meet every customer’s specific requirements.

08 Years
Experience in Pellets Manufacturing

Your Trusted Partner in Pharma Excellence
Explore Our Pharmaceutical Pellets
Services We Provide
Contract Formulation Development
Contract formulation development, product commercialization and manufacturing are focused business area for SRINAG Pharma. SRINAG Pharma is highly experienced in providing its customers a wide range of products as well as formulation development services. Our services are tailored to meet each customer’s specific expectations.
We Provide:
COA & MOA of Active Raw Material used in manufacturing of Pellets.Srinag pharma COA & MOA of supplied Pellets & Finished Formulations. Our facilities comply with the high quality standards. The high quality service level, flexible, service-oriented way of working makes us your partner of choice.

R&D Service
Our core strength is the R&D unit, which has the ability to excel in developing generics and technologically complex products through focused teams in formulation and analytical developments. Our scientists work closely with our business development team to generate innovative concepts and ideas, exploiting both market needs and synergies across therapeutic areas. We develop and apply skills to ensure the quality of the products right from the product design to the manufacturing stage. The formulation development is based on Quality by Design (QbD) principles enabling the introduction of robust, reproducible and regulatory complied products in the market. As a generic drug company, we give the top priority for building and strengthening capabilities, to excel in formulating technologically complex products in order to create strong differentiation. Our R&D team develops a wide range of generic products including difficult-to-copy formulations in the defined specialty areas and successfully developed immediate release formulations, modified release formulations, MUPS, nano products etc.

Analytical Services
Our highest level of analytical capabilities as required by the industry standards helps in benefiting our customers. Our skilled professionals utilizing modern & advanced techniques to ensure the efficiency of the testing, where the main focus is always on the product quality and safety covering all areas like Process Validation, Analytical Method Development & Validation, Stability Study, Compatibility Study etc.

Regulatory Support
As a part of our business association, our customers can take benefit of our regulatory services. Our pharmaceutical regulatory services offer the best solutions to meet all kinds of challenges for pharmaceutical regulatory filing procedures. We provide the documents in CTD (Common Technical Document) format as a part of Drug Product/ANDA filing.

Business Model
- Supply of pellets & granules in bulk
- Development of formulation dossiers
- Joint venture from development to commercialization of products
- Contract manufacturing for pellets & finished form (capsules)
- Out license manufacturing technology
Technical package is available for each product and DMF (CTD format) is ready for key products . We are interested in developing new products exclusively for customer specific needs and produce them on commercial scale.
We extend our invitation to you and your QA team to visit our facility and R &D. If any additional information is required then do let us know.























