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
Synthetic Chemistry
Piramal has been offering from mg to gm scale discovery chemistries to its customers from North America, Europe and Asia
In-vitro-Biology Services
Piramal’s in vitro Biology is designed to provide best in class support to our clients to enable their preclinical drug discovery.
In-vitro-ADME Services
Piramal's in-vitro labs provide ADME services for faster and improved decision making for our Chemistry clients
Route Scouting
Assisting our partners in discovering and developing efficient and cost effective routes
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
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 over 28 scientists including 8 Ph.D.’s dedicated to innovation in new product development, cost optimization, and novel route scouting projects
Generic API Products

A sneak peek into our facility

PARADIGM SHIFT: REMOTE AUDITS DURING THE COVID PANDEMIC

30 Sep 2020

Traditionally, most pharmaceutical companies have preferred to conduct on-site audits of their vendor partners. Seeing the partner’s facility in person and meeting the people who will be handling your product has be...

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How to develop a successful regulatory partnership with a CDMO

31 Aug 2020

A CDMO plays a critical role in developing and finalizing the CMC section of your regulatory filing. An experienced and technically sound regulatory team at the CDMO is a valuable partner in ensuring a swift and seamless product approval by variou...

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What does a pharmaceutical integrated services program entail? Key attributes to look for in an integrated services provider.

23 Jul 2020

 

As drug development gets ever more competitive, complex and costly, innovator and generic pharma companies are increasingly choosing contract development and manufacturing organizations (CDMOs) to streamlin...

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Investigative Report Writing

13 Apr 2017

According to a report by the FDA (FY2010), the third most common reason for a 483 (violation) was because of inadequate content of investigations or not completing an investigation in a timely manner. One of the most common mistakes made by the write...
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Our Facility Expanding With The Market

12 Jan 2017

According to recent trends in the market, the global contract pharmaceutical manufacturing industry is increasing at an average annual rate of 7.5% and is predicted to reach $79.24 billion in revenue by the year 2019. The market research firm, Vision...
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Maximizing Efficiency for Our Clients

02 Jan 2017

A goal of any pharmaceutical manufacturer is the pursuit of the most efficient equipment available. This equipment can increase output, reduce downtime, cut costs, and increase overall productivity while also adhering to strict cGMP requirements. The...
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