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June 03, 2026
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Advancing Sterile Liquid Development: Enabling Integrated Solutions for Small Molecules and Biologics

 
Advancing Sterile Liquid Development: Enabling Integrated Solutions for Small Molecules and Biologics

Expansions at sites in both the United States and Europe are crucial to PCI’s vision for the coming years.
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Collaborations & Alliances

Haisco, Lilly Strike Drug Development Deal

Licensing and research collaboration covers up to five programs with potential milestone payments nearing $3 billion.

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Scale Dry Powder Media to cGMP with Confidence

Discover a proven two-phase strategy to scale dry powder media while ensuring quality, consistency, and seamless tech transfer.

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Lifecore Biomedical Signs Tech Transfer Agreement for Ophthalmic

Will perform process development and technical transfer services in support of anticipated commercial manufacturing upon regulatory approval.

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Collaborations & Alliances

Cellares, TScan Partner to Automate Manufacture of TCR-T Candidate

Collaboration will apply Cellares' Cell Shuttle and Cell Q platforms to TSC-101 as a potentially scalable and cost-efficient path to commercialization.

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Flexibility in Drug Development: From Tactical Response to Strategic Discipline

How strategic flexibility enables continuity, scalability, and reliable execution in modern drug development.

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Lonza Enhances Biologics Preclinical Development Offering

DNA‑to‑IND offering leveraging GS Ori‑Go designed to deliver tox material in approximately two months, and IND readiness in as little as six months.

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Solution Center SPOTLIGHT

Kindeva

Kindeva Drug Delivery is a global contract development and manufacturing organization focused on drug-device combination products. We develop and manufacture products across a broad range of drug-delivery formats, including pulmonary and nasal, injectable, and transdermal. Our service offerings span early-stage feasibility through commercial scale drug product fill-finish, container closure system manufacturing, and drug-device product assembly. Kindeva serves a global client base from our state-of-the-art manufacturing, research, and development facilities located across the U.S. and U.K.

 

Solution Center SPOTLIGHT

Quality Chemical Laboratories (QCL)

QCL is a CDMO privately owned and operated since 1998. We excel in pre-formulation, formulation development, and delivering early phase clinical trial materials on aggressive timelines. We provide analytical development and validation, stability studies, and testing of small and large molecule APIs, finished products, and raw materials. New construction doubles our footprint to 200,000 sq. ft., expanding services into late phase clinical and small scale commercial GMP manufacturing including state of the art sterile fill-finish for both small and large molecules.