Manufacturing

Effective cleaning and disinfection along with contamination controls are imperative when operating and utilizing a cleanroom.

Symbiosis announced the successful completion of UK Research and Innovation project to enhance the manufacturing supply chain for ATMPs within the UK.

Thermo Fisher Scientific’s new Gibco CTS Xenon Electroporation System aims to provide easier scale up for cell therapies, from clinical development to commercial manufacturing.

KeyPlants has shipped a first-of-its-kind vaccine manufacturing facility to Senegal in West Africa.

New report released by USP offers a look into API supply-chain vulnerabilities.

Catalent has announced the completion of a $30 million project at its facility in Limoges, France focused on biopharmaceutical development and drug product manufacturing.

Why critical thinking must be applied before technology to ensure regulatory compliance.

CAR-T cell therapy development is a complex process that requires standardization.

Flow Eighteeen38 is receiving a €5 million (US$5.58 million) investment from its parent company, FairJourney Biologics.

Curia and the US government have entered into a cooperative agreement to expand fill/finish capability for injectable medicines.

UCB has announced it will build a new innovative gene therapy facility in Belgium.

Spectrum Chemical has further expanded its bioCERTIFIED product portfolio to support the growing global demand for new vaccines and therapeutics.

Amgen has announced the groundbreaking of its newest biomanufacturing facility in North Carolina.

G-CON’s signature standardPOD cleanrooms will now be available in Europe.

Moderna has announced that it has entered a Memorandum of Understanding with the government of the Republic of Kenya to establish its first mRNA manufacturing facility in Africa.

The Luna Probe One-Step RT-qPCR Mix with UDG is designed to enable sensitive, linear, real-time detection of target RNA sequences.

A consortium of nine development partners will support Biovac's expansion of its existing vaccine manufacturing plant capacity, while Biovac itself aims to raise funds to boost increased vaccine manufacturing capacity across Africa.

Under a collaboration, IDT Biologika and Exothera will conduct feasibility studies on scaling up the manufacturing process for viral vector-based vaccines.

Flexible and efficient methods are needed for biopharmaceutical manufacturing.

The use of bioengineering offers practical tools for the evolution of host cells.

The authors review some of the monoclonal antibody candidates that reached Phase III clinical trials but were discontinued at later stages.

CGTs offer hope for the future of treatments, but the costly manufacturing, slow turnaround time, and need for supplies hinder progress.

The continuous, aseptic fill/finish process is finding use in vaccines and biologic drugs.

Capacity concerns and regulatory compliance considerations will drive the decision about outsourcing the manufacture of clinical trial materials.

Reducing US dependency on overseas pharma manufacturing may prove critical in navigating supply chain disruptions.