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6400 Congress Avenue , Suite 1400, Boca Raton, FL, 33487, US
LGM Pharma provides CDMO services, API sourcing and analytical testing services (ATS). CDMO services include development and GMP manufacturing of oral solid dose (OSD), liquids and semi-solids. Our API division sources and manages the supply change for APIs. LGM’s ATS unit offers analytical testing on a standalone basis.
What if you could rely on one partner to source APIs, formulate and develop drug products, and manufacture at clinical and commercial scale?
Released By LGM Pharma, LLC
New imaging solution allows manufacturers to visualize internal tablet structures without cutting or altering them.
By: Charlie Sternberg
Completes multi-million dollar investment at its global headquarters in Craigavon, Northern Ireland.
New suite enables the scalable, diverse, high-quality conjugation services that customers need to advance to the next generation of therapies.
Körber’s Business Area Pharma now offers a standardized approach to connect systems and equipment to its market-leading PAS-X MES.
By: Rachel Klemovitch
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.
Establishes a Center of Excellence for Aseptic Fill-Finish Processing.
Enables Circio to further accelerate pre-clinical development towards its first therapeutic candidates.
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.
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.
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.
For this roundtable, Contract Pharma called upon thought leaders across the pharmaceutical services sector to address “3 Key Trends” impacting the CDMO industry in 2025 and beyond.
By: Tim Wright
CDMOs and CROs weigh in on today’s analytical testing outsourcing trends, including growth trends, challenges and more.
CDMOs and CROs share their most recent business highlights from the past twelve months on the oral solid dosage front.
Will increase capacity for liquid, suspension, semi-solid, and suppository drug products.
The global OSD contract manufacturing market is projected to grow, however, the sector faces challenges and is constantly evolving.
Adds endotoxin and rapid sterility testing capabilities to benefit drug developers.
LGM Pharma’s chief executive talks industry trends and the company’s continued growth as a provider of tailored API and CDMO services.
Aims to provide customers greater flexibility with a streamlined, efficient, and comprehensive solution for their manufacturing needs.
Booked 13 CDMO commercial manufacturing projects and 49 development service projects.
By: Anthony Vecchione
Analytical testing and stability services covers both drug substance and drug product.
Plus, this issue looks at Pharma Lab Trends and API Procurement and Supply Chain Management.
Gains 150 employees and more than 100,000 square feet of fully equipped facilities.
By: Contract Pharma
Expands global access to its niche API services
Hamilton J. Lenox has more than 17 years experience, and will be responsible for leading LGM’s drug development unit’s sales, business development & marketing
By: Betsy Louda
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