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5 Georg-Kalb-Straße , Pullach im Isartal, BY, 82049, DE
Hermes Pharma is the leading expert in developing and manufacturing user-friendly oral dosage forms. As a CDMO, we offer customized services along the entire pharmaceutical value chain, from new product development and formulation to manufacturing and regulatory support. For more than 40 years, healthcare companies around the globe have worked with Hermes Pharma to expand their product lines and grow their brands. Our sister company Hermes Arzneimittel has a rich portfolio of OTC brands and a long history in pharmaceutical excellence. So, we truly understand the challenges of our customers and can support them on their way to market success.
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.
Balancing safety and convenience, innovative stick pack designs offer a patient-centric solution for on-the-go dosage forms.
By: Markus Elfinger, David Kuch
Collaboration aims to develop and test future therapeutic candidates for genetic medicine, vaccines and other potential applications.
Will help meet increased demand for user-friendly oral dosage form development and manufacturing.
By: Anthony Vecchione
CDMO specializes in the development and manufacture of user-friendly oral dosage forms for healthcare companies around the world.
GMP compliant hot melt device for applying pharmaceutical coatings
By: Kai Koch
The use of electronic tongue technology helps firms reduce development times and costs by overcoming challenges associated with traditional testing panels.
By: detlev haack
Drummond brings successful track record of advancing programs to new role
Improves opening of tablet tubes used for lozenges, effervescent and chewable tablets
By: Tim Wright
Commercial production in GMP environment started to mask the sour and metallic taste of acetylcysteine
Brings easy-to-swallow medicines to U.S. market
Preparing to support a commercial launch of Xtampza ER after FDA approval
Wolfratshausen facility supports dosage forms for U.S. distribution
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