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Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products and services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines and gene therapies, made possible through Piramal Pharma Limited’s associate company, Yapan Bio Private Limited.
From discovery to intermediates, APIs & drug products, a CDMO needs expertise across multiple elements of the pharma process to deliver an integrated experience
Released By Piramal Pharma Solutions
The companies partner on antibody drug conjugates, drug substance, and drug product manufacturing services.
By: Rachel Klemovitch
Rod Ketner on Serán BioScience’s science-first culture and what biotechs should look for in a CDMO.
Released By Serán Bioscience
Investment enables GL CHEMTEC to provide preclinical and first-in-human offerings.
Jeff Speicher of PLD Pharma Services on market shifts, customer trends, and the complexities of onboarding at CPHI Americas 2025.
Released By PLD Pharma Services
Vice President of Quality and Regulatory discusses the industry's expectations of CDMOs in today’s market and advancing to support evolving needs.
Released By Grand River Aseptic Manufacturing
Robert will be responsible for creating commercial and organizational synergies between the API Solutions and CDMO operations.
By: Charlie Sternberg
Released By Mikart
Confirms the site’s full compliance with current Good Manufacturing Practices (cGMP).
Agrees to acquire two biologics manufacturing facilities from Agenus Inc. in California.
The IDMO Smart Factory will enable scalable and cost-effective cell therapy manufacturing.
CEO Owen Murray on driving innovation with high science and high service.
By: Tim Wright
Industry experts weigh in on current trends, challenges, and the future of the cell and gene therapy CDMO market.
FUJIFILM Irvine Scientific becomes FUJIFILM Biosciences and FUJIFILM Diosynth Biotechnologies will be known as FUJIFILM Biotechnologies.
Cryoport Systems is transforming the advanced therapies supply chain with integrated services that support every stage of development from early clinical to commercial scale.
Released By Cryoport Systems
Sterling will manufacture cGMP clinical material for KIVU-107 at its bioconjugation facility in Deeside, UK.
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