DISCOVERY
Piramal Discovery Solutions offers a comprehensive range of Contract Research Services from our state-of-the-art research centre in India to support drug discovery activities
Medicinal Chemistry
Piramal has been offering from mg to gm scale discovery chemistries to its customers from North America, Europe and Asia
In-vitro-ADME Services
Piramal's in-vitro labs provide ADME services for faster and improved decision making for our Chemistry clients
Non-GMP Kilo lab
Piramal’s fully-equipped kilo-lab allows for rapid development of scalable and robust chemical processes using advanced process methodologies
Analytical Support Services
The chemists at Piramal are supported by a specialist & fully dedicated analytical team which operates 24/7 with suites containing advanced analytical equipment

A sneak peek into our facility

DEVELOPMENT
Piramal offers clinical development services from Phase I to Phase III for various dosage form such as Oral solids, liquids, creams, ointments, and sterile injectable
Route Scouting
Assisting our partners in discovering and developing efficient and cost effective routes
Process R&D services
Process development for small molecule intermediates, APIs and HPAPIs
Pre-Formulation Studies
Expert approach ensures quality of drugs from discovery to commercial supply
Pharmaceutical Drug Development Services
Pharmaceutical Development of oral solids, liquids, creams, ointments, and sterile injectable.
Analytical Support Services
Range of services, including method development, stability studies, validation and transfer
Regulatory Services
Expert clinical & regulatory support across all phases of drug development programs
Clinical Trial Services
Clinical Trial Manufacturing, Packaging and Supply Services using our global network

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MANUFACTURING
Piramal offers contract manufacturing for API, HPAPI and a wide variety of dosage forms. Our global manufacturing sites located across North America, Europe and India offer the highest standards of quality and service to the customers
API Manufacturing
We provide the manufacture and supply of Active Pharmaceutical Ingredients (APIs) on an integrated manufacturing model across North America, Europe and Asia
HPAPI
Piramal Pharma Solutions offers the development and manufacturing of High Potency API services from its Riverview facility
Finished Dosage Manufacturing
Lifecycle Management
With very small quantities of active pharmaceutical ingredients (API) or drug-able candidate molecules

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ANTIBODY DRUG CONJUGATION
Piramal is the global leader in delivering customer-centric solutions in the field of Antibody Drug Conjugates (ADCs) and other bioconjugates to global biopharmaceutical companies
Proof-Of-Concept Studies
Piramal offers a fast-track early stage development service for your ADC programmes. Whether you are selecting your candidate mAb, linker or toxin
Process Development and Scale Up
Piramal offers ADC process development and scale-up through Tox manufacture and into GMP manufacture
ADC Manufacturing
World-leading multi-product facility for clinical and commercial manufacturing of antibody drug conjugates (ADCs)
ADC Fill/Finish
Piramal offers aseptic filling of ADC drug product through our FDA-inspected state-of- the-art manufacturing facility in Lexington, KY
Analytical Development Services
Analytical development team covers a wide range of analytical methods from small molecule analysis through to cell killing assays and ELISA development

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GENERIC APIs
Piramal’s Generic API division offers an indigenous basket of off-patent APIs for global markets. With the declining pipeline of new drugs in the pharmaceutical industry, our customers are looking for off-patent APIs with competitive cost and quality
Mumbai, India
We have an experienced team of 28 scientists including 8 Ph.Ds dedicated to innovation in new product development, cost optimization, and novel route scouting projects
Generic API Products

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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.

Shanghai, China - Sourcing Office

Do you have a generic API development or manufacturing requirement?