R&D Capabilities

We have an experienced team of over 80 scientists (with over 20 Ph.D.’s) dedicated to innovation in new product development, cost optimization, and novel route scouting projects. The R&D team develops novel/non-infringing process for APIs and is supported by a state-of-the-art, ‘best in class’, analytical research capabilities.

R & D capabilities include:

  • Development of environmental friendly processes
  • Development of chiral APIs
  • Ability to comply with ICH guidelines
  • Synthesis, Isolation and characterization of impurities
  • Expertise in handling pyrophoric reagent
  • Expertise in cryogenic reactions (-40 to -100°C)
  • Expertise in handling organometallic reactions

Locations

Our APIs are manufactured at US FDA approved sites across the globe- sites which have impeccable quality records: no warning letters or import alerts on any Piramal sites since inception of the company (1988 until today). On time readiness and delivery has been our strength through the combination of R&D innovation and fully integrated supply chain that levers the manufacture of intermediates in-house to help control cost and meet aggressive timelines. The API manufacturing sites are US FDA, UK MHRA, PMDA Japan, WHO GMP approved. The sites have API Regulatory submissions across the globe including e-CTD.

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experts

Spread over 100 acres, Piramal Pharma Solutions' state-of-the-art facility at Digwal is located 70 miles from the city of Hyderabad. With over 30 years of operational excellence, the facility has been supporting the manufacturing of API's and advanced intermediates.

Aurora, Canada

This is our site for development and GMP manufacturing for complex pharmaceutical NCEs. It is located in Aurora, 50 kms north of Toronto.

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Lexington, USA

The Coldstream Laboratories manufacturing facility utilizes isolator technology for aseptic processing in a 22,000 square foot state‐of‐the art building.

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Riverview, USA

Our State-of the-Art FDA licensed cGMP facility in Riverview, USA, has over 50 years of extensive experience in delivering robust cGMP manufacturing processes..

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Grangemouth, UK

Grangemouth, UK is a USFDA and MHRA approved site dedicated to the contract development and manufacturing of Antibody Drug Conjugates since 2004.

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Morpeth, UK

The Pharma Solutions Morpeth site is one-of-a-kind US FDA and UK MHRA approved facility offering integrated services across the pharmaceutical value chain.

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Ahmedabad, India

Ahmedabad, India site was established in 2009. It is a MPA, Sweden approved and FDA approvable facility for development..

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Ahmedabad, India

Piramal Discovery Solutions site is located in Ahmedabad, India and provides a comprehensive range of early stage drug discovery services

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Mumbai, India

Operational since 2005, our Mumbai site is fully equipped for development of all liquid dosage forms both Sterile and Non-sterile.

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Pithampur, India

The Pithampur formulations site is a Greenfield project set in 1992 by Piramal Pharma Solutions. The US FDA and UK MHRA approved facility..

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Ennore, India

Ennore is identified as the India centre for development and early phase projects located near the Chennai port. The site is spread over an area of 75 acres..

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Digwal, India

It is a dedicated and multipurpose plant identified for custom manufacturing and development for late phase API’s and advanced intermediates.

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Mahad, India

It is a multipurpose plant identified for manufacturing of straight Vitamins & Vitamin Mineral Premixes.

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Aurora, Canada

This is our site for development and GMP manufacturing for complex pharmaceutical NCEs. It is located in Aurora, 50 kms north of Toronto.

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Lexington, USA

The Coldstream Laboratories manufacturing facility utilizes isolator technology for aseptic processing in a 22,000 square foot state‐of‐the art building.

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SHANGHAI, CHINA

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OUR LOCATIONS

With a versatile, fully integrated network of development and manufacturing sites across North America, Europe, and Asia. Learn more about how we can serve your needs locally, wherever you are

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