We manufacture, supply and distribute commercial formulations from our facilities in UK and India for Oral Solids and Lexington, USA for Sterile Injectables. We are a trusted manufacturing partner to leading biotech, small and virtual pharmaceutical companies as well as mid-size and big pharmaceutical companies. Our scalability is defined from Pilot level to Commercial level to serve customers at every stage of drug lifecycle from manufacturing perspective. We leverage our Global network of manufacturing sites and are successful in supplying commercial formulations to the US, Europe, Japan and Asia Pacific markets.

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Cytotoxic and Potent Compounds

Piramal’s facilities and skilled team of experts can help you safely and efficiently turn your high-potency project into a success. We routinely specialize in formulating highly toxic compounds, such as cytotoxics, hormones, and steroids into safe and effective liquid or lyophilized drug products.

We employ state-of-the-art mobile isolator technology in our manufacturing facility to provide a physical barrier that protects our staff from toxic substances and encloses your product in a Class A Environment. Similar fixed isolators are used in our development labs to mimic manufacturing operations and enable formulation and analytical development on toxic substances. Through the use of these high containment “glove boxes,” our scientists create and maintain a controlled sterile envelope that enables us to process potent drug classes including cytotoxins, steroids, hormones, and acutely toxic substances.

Additionally, we can assist our clients in evaluating the hazards associated with their compounds through our New Product Assessment program to determine an Occupational Exposure Limit (OEL). Our operating systems require that all direct product contact equipment is either dedicated or disposable in order to provide robust protection against cross-contamination.

With a client base that includes large and small pharma, biotech’s, animal health, academic and government institutions, Lexington has expertise to support manufacturing from pre-clinical to routine commercial manufacturing.

From simple solutions to the most complex formulations we have successfully supported over 100 liquid and lyophilized drug candidates for both large and small molecules.

Cytotoxic and Potent Compounds Location

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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