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1550 Olympic Drive , Athens, GA, 30601, US
Purisys is a North American-based API CDMO and provider of generic and custom APIs, reference standards, and analytical services for global emerging biotech to large pharma customers who seek small volume/high-value API services for both controlled and non-controlled therapeutics. Purisys APIs serve preclinical through Phase IIa and commercial.
Why pharma needs automated AI security now.
By: Frank Balonis
Welcomes Brian Riley as President and Chief Technical Officer, Joanne Lager, MD as Chief Medical Officer, and Adrian Chaisson as Chief of Staff.
By: Charlie Sternberg
Dr. Abdul Mutlib is appointed the President of Frontage Laboratories, Canada, and will spearhead growth as he continues to serve as Chief Scientific & Strategy Officer.
By: Rachel Klemovitch
Strengthens BioMarin's enzyme therapies portfolio, adding a late-stage enzyme replacement therapy, INZ-701.
Forms a rare tumor business for Merck KGaA, Darmstadt, Germany, including SpringWorks’ portfolio and pimicotinib.
The U.S. launch of Conexxence and Bomyntra follows the FDA’s approval in March 2025.
Richard Thakor and Daniel Anderson will speak at the event in November.
Strengthens its global particle engineering capabilities.
Will manufacture SurVaxM, a novel immunotherapeutic vaccine designed to treat glioblastoma, for use in clinical trials.
Integrate Keystone’s Key-Pak child-resistant blister cards with Med-Con’s medication adherence prompting and monitoring application.
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.
Collaboration aims to discover and develop novel therapeutics for cardiovascular disease using Novartis’ ProFoundry Platform.
It is the only ready-to-use liquid immunoglobulin therapy with (IgA) content and is set for commercialization in 2026.
The companies have released the first batch of Novalgen’s next-generation T-cell engager for first in-human clinical trials.
The collaboration now is progressing to the in vivo preclinical stage.
Will further expand its domestic capabilities to develop, produce and deliver medicines.
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.
The company’s label updates are for its CAR T cell therapies, Breyanzi and Abecma.
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.
Hervé Hoppenot will retire after 11 years of leading the company through major expansion.
Will commence cell therapy process development and clinical manufacturing services at AGC Inc.’s Yokohama Technical Center.
Agreement to support future studies investigating the combination of ateganosine and atezolizumab for safe and effective cancer treatments.
Will develop and commercialize a potential treatment for obesity and metabolic disease based on technology licensed from the U.S. Department of Veterans Affairs.
Addressing increasing complexity, cost of drug development, and navigating regulatory compliance.
By: Kristin Brooks
Will add further sterile fill/finish capacity over the course of the next year.
Agnus joins Bora Group from KBI Biopharma, where he led global business development.
ST16 Semi-Automated Aggregation Station combines software and flexible hardware to help optimize productivity, improve operational efficiency and streamline processes.
J.D. Mowery brings nearly 25 years of experience in the CDMO and biopharmaceutical industries.
Will combine their biomanufacturing facilities to create a global service for biologics development and supply.
The newly acquired facility provides drug product manufacturing services for sterile injectables.
This strategic partnership provides end-to-end visibility and best-in-class track and trace for Praxis’s customer base.
This integrated solution follows the company’s acquisition of Pharmacontrol Electronic and combines technologies.
This acquisition enhances Systech’s product offerings and enables it to offer a more comprehensive product portfolio to its customers.
Offers quick compliance, avoids delays, and optimizes production with multi-scan and mobile flexibility.
Will bring its total U.S. capital expansion commitments to more than $50 billion since 2020.
Surging demand for specialty drugs, alongside the prevalent use of generic medications are driving growth.
In this case study, the determination of substitution of 2-CTC resin is discussed.
Released By Almac Group
Massive overhaul in works to embed greener processes.
By: Soman Harachand
The transaction aims to strengthen and broaden Olon’s product offering with a focus on the most strategic areas.
India has an opportunity to strengthen its position in the global pharmaceutical market.
By: Vladislav Vorotnikov
Leverages peptide drug substance discovery and clinical development expertise.
New identity signifies the integration of the two manufacturing plants, Cipan and Rovereto, in the API production and distribution space.
Kit contains focussed library of 10 double stranded RNA Ligase enzymes selected from an extended RNAL enzyme panel.
A Q&A with Eric Neuffer, Global Head of Drug Substance Sales, Evonik Health Care.
Released By Evonik
Invests in R&D activities at Vertolaye site to increase production of morphine that could increase productivity between 20% and 30%.
Released By PeptiGrowth
The installation of an advanced mill for grinding finished APIs will significantly increase production capacity of the finishing area.
By: Anthony Vecchione
Partnership aims to expand the use of Ripple's Epidel platform beyond ophthalmic applications.
In the recent process development efforts one of the major time-consuming steps was significantly improved.
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