Centric pharma is is a pharmaceutical company engaged in development, manufacturing and marketing with creating value for all stakeholders by manufacturing high quality Generic APIs, Custom synthesis of APIs, Intermediates and starting materials. We clearly understand our customer’s needs and use cutting edge technology to present innovative solutions by a team of Pharmaceutical Professionals with more than 25 years of experience in the industry.
Centric pharma was established by a set of pharmaceutical professionals who have rich experience in pharmaceutical companies. We have expertise in pharmaceutical products.
What we do?
We are a team of experts in developing cost efficient robust process for KSM’s, intermediates and API. We are a customer centric organization focused on customer delight. We are a team of dynamic and agile members with a focus to meet customer needs and their deliverables on time.
In our endeavour of understanding the needs of the patients, we develop and provide healthcare in the areas of:
- Anti-Retro viral (Anti-HIV)
- Anti-cancer (Oncology products)
To become responsible business partners of pharmaceutical companies.
To enable pharmaceutical companies to provide affordable high quality medicines to all
- Manufacture and supply of Gram to tonnage of KSM’s, intermediates and API
- Technology development for complex API and its intermediates
- Contract manufacturing of KSM’s, intermediates and API.
- Technology transfer, scale-up, process validation and DMF filing.
- Complex Impurity synthesis, characterization and supply.
- Scale up studies in Kilo lab and pilot plant, process validation and DMF filing
CRO & CMO
We have R&D facility and GMP manufacturing facility apart from that we also have collaboration agreements with many GMP manufacturing and analytical facilities. We provide following services:
- Selecting the cost effective robust Route of Synthesis (ROS)
- Gram to tons supply
- Scale up studies in Kilo lab and pilot plant
- Process optimization
- Analytical development and validation
- Process validation
- Impurity characterization
- Tech pack preparation and technology transfer
- DMF documentation and filing
We support our customers for developing process and supply materials from gram scale to tonnage, we also work on FTE models with MNC’s.
Regulatory Query resolutions
We support our clients with regulatory query resolutions, through our deep understanding on regulatory and product knowledge.
We service customers for supporting the following
- Analytical method development and validation
- Instrument calibrations
- Impurity characterizations
IP and Regulatory Services
- Provide IP evaluation for process and provide guidance to design the process
- Support for regulatory documentations and filing
- Handle regulatory audits