Bharat Parenterals Ltd. is a Gujarat based pharmaceutical company, established in 1992 by Mr. Ramesh Desai, who started the company with a vision of making world class affordable medicines and to take it to the forefront of contract manufacturing units in Gujarat.

A WHO GMP & an ISO 10002: 2014, 9001: 2015 certified pharmaceutical company, Bharat Parenterals Ltd has traversed a long way in order to be recognized as one of the fastest growing Pharmaceutical Companies in India today.

Growing at a fast yet steady pace, the second-generation contract development & manufacturing organization, led by Mr. Bharat R Desai, is well on its way to becoming a leader in New Age Formulations, both nationally and internationally.

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Wide Range of Products

With over 800 products spread over more than 20 different categories

Accreditation & Certificates

With over 25 years of experience in the industry, we have received numerous accolades and earned a variety of accreditations

World-Wide Reach & Services

With clients from over 35 countries, we have the quality and ability to serve people across the globe







Our Operations

A glimpse of how we do what we do

Manufacturing Infrastructure & Facilities

The company has a State-of-art manufacturing facility spread over 30,000 sq.ft area with large batch size capacity for General: Tablets, Capsules, Oral Liquids, Small Volume Parenterals, Dry Powder Injections, Eye drops, Ointments, Lotions, Creams, Powders & a separate Unit for B-Lactam : Tablets, Capsules, Dry syrups, Dry Powder Injections.
All operations are thoroughly monitored by Quality Assurance Department with effective quality management systems in place.

Formulation, Research and Development

Our advance Formulation & Development Department forms the foundation for our Quality Manufacturing output & was recognized by Department of Scientific & Industrial Research (DSIR), New Delhi in August-2010.

Quality Assurance/Quality Control

All operations are thoroughly monitored by Quality Assurance Department with effective quality management systems in place.

Regulatory Affairs

Pharmaceutical Regulatory Affairs department ensures that the organization complies with all of the regulations and laws pertaining to drug research and development . It works with federal, state and local regulatory agencies on issues affecting drug research and development and manufacturing. It design and implement innovative and global regulatory strategies in order to expedite product development and registration of product in respective regulatory authority.

Our Clients