Bharat Parenterals Limited is a WHO GMP & an ISO 10002: 2014, 9001: 2015 certified pharmaceutical company incorporated in 1992 with its manufacturing facility in Gujarat (Vadodara), India. A progressive manufacturing organisation, we are fully integrated with in-house R&D, Business Development, Manufacturing, and Regulatory Compliance capabilities. We have a legacy of more than 25 years of expertise in: Custom Manufacturing, Formulation & Development, Analytical Method Validation, Regulatory Services, Technology & Process Transfer and Stability Studies. We also offer Contract Research and Contract Manufacturing services. The company endeavors to manufacture a rich array of quality formulations supported by its strong Formulation & Development department and state-of-the-art manufacturing facilities for its own markets and for several reputed organizations in India and world wide. BPL is committed to implementing Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in its pursuit of continuous business growth. .With over 800 products spread over more than 20 different therapies and clients from over 35 countries in Africa, South East Asia, LATAM and CIS, we have the quality and ability to serve people across the globe. The company's State-of-art manufacturing facility is spread over 30,000 sq.ft area with a 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.
Eastern Europe; Middle East; Asia; Africa; Central/South America
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