ABOUT US

Headquartered in Chandigarh, India, Essix Biosciences Limited, today is a global manufacture of APIs, Intermediates and formulations (through group collaboration). We cater to the API needs of regulated markets including GMP PLANT.

Today, Essix Biosciences Limited, is a significant player in manufacturing APIs towards Cardiovascular health, Antihistamine, Antidiabetic, Antipsychotic, Antimigraine, Parkinson’s disease, Antineoplastic, ADHD Symptoms, Analgesics, Alcohol Abstinence and Bone Resorption Inhibitor.

Corporate Social Commitment and Public Service is at the upmost priority list of the Company. Over the years serious efforts have been directed towards making a meaningful contribution to uplifting and transforming the lives of the community and the underprivileged. The Company is also extremely conscious of its duty and responsibility towards the environment.

Environment Reports

You can download our current environment reports in which you’ll find comprehensive information about our efforts, how we measure the overall effect we have on the environment and the progress we’ve made over the last period of year.

SIX-MONTH PROGRESS REPORT
April 2023 – September 2023
(PDF FILE, 8 MB)

ARCHIVE REPORTS​

October 2022 – March 2023
(PDF FILE, 11.8 MB)

April 2022 – September 2022
(PDF FILE, 5.8 MB)

October 2021 – March 2022
(PDF FILE, 5.7 MB)

WHY CHOOSE US

Essix Biosciences’s chemical development scientists have the skill and experience to meet a wide range of outsourcing needs from the custom synthesis and scale-up of an existing route, to identification and development of new manufacturing routes. Each step of the development process is staffed by a highly qualified technical team that includes chemists, engineers and EHS. For every step, clinical phase appropriate objectives are identified and complete hazard assessments are performed to allow for safe production of your compounds.

OUR PORTFOLIO

We manufacture a wide range of APIs based on the appropriate control system which complies with the regulations of international GMPs guidelines. Production activities operate daily at our factories that are experienced in obtaining FDA approval by paying special attention to a variety of points such as not only high quality but also productivity, costs, safety, environmental influence, etc.

OUR Certifications

Certification of Registrations

Our Services

We achieve the consistent supply of safe and secure APIs by implementing three principles based on

High Quality
High Added Value
Flexible Service