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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.
How Piramal Pharma is shaping resilient, patient-centric development across OSDs, HPAPIs, and sterile injectables.
Released By Piramal Pharma Solutions
From discovery to intermediates, APIs & drug products, a CDMO needs expertise across multiple elements of the pharma process to deliver an integrated experience
The S&P Global CSA analyzes companies on environmental, social, and governance performance, governance maturity, and long-term value creation.
By: Charlie Sternberg
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.
Hovione’s chief executive shares his vision for establishing and maintaining leadership as a CDMO.
If there’s one constant in drug development today, it’s that the pressure of speed to clinic is only ever increasing.
Released By Upperton
A biotech approached Upperton with a formulation developed externally by another CDMO.
Join us on January 29th for a data-driven look at the trends shaping CDMO marketing in 2026.
Combines Transcenta’s continuous biomanufacturing platform and EirGenix’s bioprocessing and CDMO expertise.
By: Kristin Brooks
As small-molecule pipelines grow more complex, formulation has become a decisive factor in whether promising compounds reach patients.
Released By Bend Bioscience
By: Tom Morford
Implements a multi-step action plan to ensure regulatory alignment with the latest NDSRI guidelines.
The Future of Oral Solids explores how innovation, advanced manufacturing, and integrated CDMO partnerships are reshaping the oral solid dosage (OSD) landscape, now and in the years ahead.
Released By Adare Pharma Solutions
Codis launches as a global CDMO specializing in spray drying, amorphous solid dispersions, and particle engineering, uniting Particle Dynamics and EUROAPI’s former Haverhill facility under one brand.
Released By Codis
Over the past 20 years, the company has grown from a small startup into a trusted CDMO partner for biopharma companies worldwide.
A guide to the advantages and disadvantages of One-site vs Multi-site/Global CDMOs
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