
Financial commitment will go toward expanding the CDMO’s integrated antibody-drug conjugate services.

Financial commitment will go toward expanding the CDMO’s integrated antibody-drug conjugate services.

With the acquisition, Merck’s US and Canada life science business aims to further increase its viral vector manufacturing capabilities.

The CDMO will run the active pharmaceutical ingredient pilot plant in Sandwich, UK, along with development laboratories.

The agreement is expected to focus on cell manufacturing processes, with potential for sharing tech with academia, startups.

The facility, company says, will be its first that covers end-to-end ADC production.

The CDMO’s latest business venture reaffirms its commitment to the development of novel radiopharmaceuticals.

The company has financially committed more than $3.8 billion since the COVID-19 pandemic into keeping the medication and vaccine production process in France.

The development project adds an additional 157,500 square feet to the existing facility in the process.

The CDMO’s Bedford, NH facility will welcome a new isolator filling line—along with twin lyophilizers—as part of a multi-year, $100 million capital investment project.

The CDMO’s boost in production will be centered around pharmaceutical products.

The company adds a top-10 CDMO to its portfolio in the process, while also expanding its commitment to the pharma industry.

The deal further grows the Big Pharma company’s US production capabilities, especially when it comes to global parenteral products.

The acquisition initiates a long-term agreement with Beacon Therapeutics, highlighted by clinical and commercial AAV production.

The purpose for the deal, the CDMO says, is to meet the demand for commercial mammalian contract manufacturing.

A proposed Senate bill is intended to protect citizens’ private health and genetic information.

The CDMO’s multi-million-dollar expansion project features commercial manufacturing suites and peptide manufacturing plants.

The purchase boosts the parties’ sterile liquid manufacturing capabilities.

The partnership revolves around meeting various agency standards and industry requirements pertaining to the drug development and manufacturing lifecycle.

The new seals include sustainable film material containing recyclate content of up to 90%.

Properly supporting market access for a newly launched product with a single indication is challenging. Doing so for multiple indications, or supporting subsequent indications, can have a compounding effect on the degree of difficulty for getting everything right.

RLG Healthcare will focus on specialty pharmaceuticals and healthcare packaging.

The pharma powerhouse is investing $300 million in a plant that could be vital for the future cancer trials.

The deal is expected to help boost supply of Wegovy.

An analysis of the two main new models for pharmacy—unique direct—to-consumer for brands and cash pay for generics—and what members of industry think about them.

Leading experts in the sector explore the value of third-party logistics providers when it comes to fortifying pharmaceutical supply chains.