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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 need for advanced, patient-friendly drug delivery solutions has never been more urgent.
Launches hot melt extrusion platform at its Regensburg, Germany facility.
By: Charlie Sternberg
Strengthens Ofichem’s integrated development offering, enabling it to offer broader, deeper support from early-phase development through to GMP production.
The addition of 62,000 square meters of new development in 2026 will more than double the total footprint of the site to 108,000 square meters.
This investment expands Delpharm’s Saint-Rémy site.
By: Rachel Klemovitch
Why pharma needs automated AI security now.
By: Frank Balonis
Strengthens its global particle engineering capabilities.
Pharmaceutical service provider expands its footprint in the greater Chicago area.
Released By Vetter Pharma International
The company is investing $90 million to expand two U.S. facilities to enhance capacity and efficiency.
Villain offers extensive expertise in peptide and oligonucleotide development and manufacturing.
The companies have released the first batch of Novalgen’s next-generation T-cell engager for first in-human clinical trials.
EVP & COO Todd Nelson reflects on Porton J-STAR's defining milestones, global network strategy, and what’s ahead as the company enters its third decade.
Released By Porton
The clinical site is expected to be completed and ready for media fill by the end of 2029.
Is purpose-built for manufacturing high-quality plasmid DNA and viral vectors.
Partnership expected to improve yield and upgrade analytical methods ahead of clinical use and regulatory submissions.
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