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18655 Krause Street , Riverview, MI, 48193, US
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the entire drug life cycle. Leveraging an integrated network of facilities in North America, Europe, and India, we provide a comprehensive range of drug discovery services, early phase active pharmaceutical ingredient (API) and formulation development services, and late phase and commercial API and formulation services. We also offer specialized solutions for highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptides, potent solid oral drug products, vaccines, and biologics/bio-therapeutics.
Advances in payload-linker technology have made ADCs a major therapeutic modality, prompting drug developers to strive for greater selectivity and safety in the next wave of ADCs. Payload-linker selection is vital to these initiatives, making the choice of an experienced development and manufacturing partner a key decision in the highly competitive ADC market.
Released By Piramal Pharma Solutions
How Piramal Pharma is shaping resilient, patient-centric development across OSDs, HPAPIs, and sterile injectables.
From discovery to intermediates, APIs & drug products, a CDMO needs expertise across multiple elements of the pharma process to deliver an integrated experience
Site has produced hundreds of distinct bioconjugates and supports clinical, commercial, and non‑GMP manufacturing activities.
By: Charlie Sternberg
Enables more flexible and customizable dosing options for critical oral drug therapies, including modified release drug delivery.
The S&P Global CSA analyzes companies on environmental, social, and governance performance, governance maturity, and long-term value creation.
Underscores the facility’s dedication to upholding the highest standards of quality across operations.
Agreement expands Piramal’s payload-linker platform and bioconjugate abilities.
Provides the Morgpeth facility’s Formulation Development Team with an important tool for developing fixed dose combinations and modified release drug delivery.
The U.S. Food and Drug Administration (FDA) approved WIDAPLIK on June 6, 2025.
The investment provides NewAmsterdam Pharma with commercial capacity for a fixed-dose combination of obicetrapib and ezetimibe to meet potential commercial demand.
The CDMO is preparing for its New Jersey facility to become fully operational this year.
By: Patrick Lavery
Aims to enhance capital efficiency, improve operational focus and position each business to independently create and capture value.
Practical guidance for sponsors to extract meaningful insight—and avoid costly surprises— when vetting CDMO partners.
Forward-thinking CDMOs are redefining collaboration by helping brand owners translate consumer insight into differentiated, compliant products
Emerging modalities and staying one step ahead of the latest trends were topics of interest at DCAT Week 2026.
From quality-led differentiation to digital alignment and regional strategy, CDMOs are redefining how they compete in a more constrained, complex outsourcing landscape.
Aims to become one of the world’s top three injectable CDMOs
Davuluri will position the CDMO as a premier global API process development and commercial manufacturing specialist.
Independent recognition strengthens Vetter’s position as a trusted, high-performing CDMO Â
Released By Vetter Pharma International
How CDMOs must evolve beyond Annex 1.
Released By Grand River Aseptic Manufacturing
CCO Arul Ramadurai on Axplora’s strategy for high-potency growth.
Unveils revamped brand identity.
Global benchmarking report recognizes the most capable CDMOs in the ADC sector across innovation, growth, and end-to-end service excellence.
Released By Abzena
Agilent Advanced Therapeutics brings together BIOVECTRA, in Canada, and Nucleic Acid Solutions in Colorado.
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