Manufacturing & Packaging

Further expansions of the pharmaceutical development and manufacturing services of ten23 are happening at the BASE and VIVA facilities to continue to support complex sterile product development, testing, and manufacturing.

How drugmakers can navigate the program’s pricing challenges and regulatory developments.

Expansion allows facility to provide E2E services in one location, including commercial manufacturing.

The company will occupy approximately 62,000 square feet of the new building.

The plant— dedicated to cell and gene therapy development—welcomes additional warehouse space, and aims to meet commercial needs.

How the ‘fight-for-the-dollar’ is coming and likely will impact the bundled pricing of industry stakeholders.

Companies' emphasis on delivering pharmaceuticals is evolving into a collaboration focused on healthcare outcomes.

The key questions and considerations for drug manufacturers pursuing an effective alternative distribution model.

CDMO’s Taoyuan City plant is set to provide customers with products ranging from emulsions to gels.

CDMO’s Turku addition will span over 69,000 square feet and support the production of ATMPs.

Sterile injectable plant—struck by tornado—is currently being assessed.

The 19,500 square-foot warehouse will support API manufacturing activities, all the way through commercialization.

The debut will be the CDMO’s first fully automated sterile injectable manufacturing line at the Wuxi, China site.

Report reiterates CDMO’s commitment to net-zero emissions.

Goal of the deal is to boost the production of oral dosage forms.

The 50,000 square-foot facility will feature 10 new manufacturing sites with commercial capabilities.

Platform is expected to streamline the label management process.

Initiative to support developing manufacturers launch new products.

According to a recent TMR study, there is an expected CAGR increase of 5.6%.

The 200,000 square-foot manufacturing plant—coming early next year—is expected to help boost capacity of pharma packaging materials.

The series’ marking heads help deliver codes to support both product traceability and anti-counterfeiting efforts.

Expansion expected to create additional production capacity, company says.

Changes to 3PL’s facility feature newly-converted controlled room temperature pallets.

CDMO’s new facility is expected to be operational by April 2025.

The accreditations—granted to the company’s sites in the US, LATAM, and Canada—are given for compliance with specific pharma manufacturer guidelines.

Decision is anticipated to boost operational efficiencies for the CDMO.

Company is expanding its manufacturing capacity for drug substance and drug product at its sites in Leverkusen and Wuppertal, Germany.

New PC column explores commercialization trends and how pharma can adjust to the new squeeze of market, regulatory, pricing, and gross-to-net pressures.

Company’s latest report reveals future plans, powered by efforts to divert more of its air shipments to sea.

New fill-finish plant strengthens nation’s reputation as an APAC biomedical hub.