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April 27, 2026
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Unique Products, Unique Solutions: Why Flexible, Tailored CDMO Support is a Non-Negotiable in Sterile Fill-Finish

 
Unique Products, Unique Solutions: Why Flexible, Tailored CDMO Support is a Non-Negotiable in Sterile Fill-Finish

How the right CDMO partnership reduces risk, accelerates timelines, and protects product integrity from vial to patient.
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Top Headlines

Breaking News

Lilly to Acquire Ajax Therapeutics Inc.

Ajax's lead asset, AJ1-11095, is an investigational, once-daily oral, first-in-class Type II JAK2 inhibitor currently being evaluated in a Phase 1 clinical trial.

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[VIDEO] Inside the Future of CDMO Partnerships

GRAM's VP of Quality and Regulatory discusses the industry's expectations of CDMOs in today’s market and advancing to support evolving needs.

Breaking News

PCI Pharma Services Invests in Infrastructure to Bolster Domestic Manufacturing Footprint

Aims to deepen its sterile fill-finish and advanced drug delivery capabilities.

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Promotions & Moves

AES Cleanroom Technology Taps John Groth as Chief Revenue Officer

Groth will oversee business acquisition, sales, strategic partnerships, and commercial operations.

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[VideoBite] Overcoming Solubility Challenges at Hovione’s Expanded NJ Site

David Basile of Hovione discusses expanded spray drying capacity in East Windsor and the benefits of integrated development, scale-up, and manufacturing at a single U.S. site.

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Collaborations & Alliances

BD, Suttons Creek Partner to Support Pharma & Biotech Companies Developing Combination Products

Under the collaboration, BD’s device-agnostic combination product testing organization is complemented by Sutton’s Creek combination product development and systems integration expertise.

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Introducing Contract Pharma STREAM: Your New Hub for Pharma & Biopharma Insights

Access expert-led webinars, VideoBites, and eBooks focused on manufacturing, supply-chain, drug development, and more.

Featured Resources

Solution Content Centers SPOTLIGHT

Sentry BioPharma Services, Inc.

Sentry BioPharma Services, Inc. (Sentry US) protects product SISPQ by offering compliant pharmaceutical services, including cGMP temperature-controlled storage, controlled substance management (CS III-V), clinical/commercial labeling and secondary packaging. Sentry also provides import/export optimization by leveraging our end-to-end GxP logistics, global distribution and Foreign Trade Zone expertise. Sentry’s status as a US Foreign Trade Zone enables products from outside the United States to be received and held within cGMP storage, pending approval for importation from the FDA, CBP and DEA. Sentry is VAWD accredited, licensed in all US states and inspected by the FDA, along with numerous international authorities. Sentry’s newest facility in Columbus, IN provides stock splitting risk mitigation services and will offer additional cGMP offerings in 2026.

 

Solution Center SPOTLIGHT

August Bioservices

August Bioservices is a US-based CDMO focused on delivering high-quality development and manufacturing solutions for sterile injectables. With state-of-the-art facilities and advanced technical expertise, August Bio offers a seamless integration of services that span from early-stage development to commercial-scale production.