
Contract Chemistry: Custom Synthesis for Toll Manufacturing of Drug Intermediates & Fine Chemicals
September 05, 2018
When it comes to the pharmaceutical industry, the old adage “if you want something done right, do it yourself” doesn’t necessarily apply. Big Pharma, as well as biotech and drug development companies, rely on an intricate network of partnerships in the academic, business and technical realms to get drugs through the extensive clinical trial process and into the market.
Custom synthesis is one of the options open to drug developers in need of the active pharmaceutical ingredients (APIs) to make their products effective. If it is impossible or impractical for a company to make these molecules and compounds in-house, a chemical specialist that offers custom synthesis will often be brought in to do the job. For the most part, these contracts are carried out under strict confidentiality agreements and strict delivery deadlines are part of day-to-day operations.
Shree Ganesh Remedies Limited is an India-based pharmaceutical manufacturing & service company that specialises in chemical synthesis for customers in the pharmaceutical industry. Based on our custom synthesis technology accumulated over a long period, we respond to requests for any type of outsourcing smoothly, from development stage to production.
Thanks to completion of a new plant for large-scale production, we have the
production capacity to respond flexibly to various kinds of needs, from
small-scale to large scale production, along with existing large automated
facilities for Pharmaceutical Drug Intermediates and Fine Chemicals, and high-performance multi-purpose facilities.
SGRL’s manufacturing facilities are ISO 9001, 14001 & 180001 Certified. Under
high quality control system that conforms to c-GMP and ICH standards and based
on DMF, CEP registration, we provide outsourcing services that will satisfy our customers.
In addition, we proactively engage in EHS (Environment, Health, Safety) investment.
Flow of Custom Manufacturing Services
The person responsible for experimentation will handle test manufacturing, commercial scale production test, and subsequent correction consistently.
In this way, we avoid time loss, communication error, etc., due to handover.