
CDMO’s future greater Boston facility to expand cGMP manufacturing capacity, accelerate commercial drug supply

CDMO’s future greater Boston facility to expand cGMP manufacturing capacity, accelerate commercial drug supply

Manufacturing center expected to integrate data analytics, machine learning into production process

Marks the fifth shot to receive emergency approval by Indian health authorities

Sets the scene for a messenger RNA production facility in Canada

Michigan site adds 110,000 square feet to its production footprint as company aims to meet additional demand

Acquisition boosts C> portfolio by 622,000 square feet, as CDMO eyes global expansion

CDMO's North Carolina development adds over 3,700 square feet worth of manufacturing space, equipment

Among focal points, New Jersey location will support clinical research, pharmacovigilance

Supply will start to become available in Q4 of this year, pending approval by EMA

CDMO says BFS capacity can now reach over 2 billion units yearly

Sector is expected to be driven by a rise in drug development and regulatory approvals for advanced therapies

Acquisition of US partner establishes Sanofi's plan to advance messenger RNA technology for vaccines, therapeutics

Guidance supports cross-industry collaboration for improved interoperability

Partnership to focus on gains for clinical development and commercialization through patient data curation and real-world data

June report reveals an 8% boost to air cargo market

Baltimore facility production was stopped after FDA flagged millions of contaminated doses

Private equity companies see the sector as having a valuable ROI, according to study

Pharmacy discount card company and e-commerce specialist team up on new Rx-med procedures channel

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German drugmaker also plans to set up manufacturing facilities in Africa

Deal for antibody developer expected to be largest ever for scientific instrument maker

In-house center eliminates the need for a contract manufacturer, company says

Acquisition is centered on market access and patient advocacy

European Commission to determine if Spikevax will receive emergency approval for children aged 12 to 17

Report notes that companies particularly look to vendor support for technologies such as 5G, IoT, and blockchain

3PL company's QuickSTAT site manages cell and gene therapies, vaccine storage, among other roles

Per agreement, facility will be producing over 100 million doses annually for use in African Union

Robotic filling and capping equipment to be installed in NIBRT’s global bioprocessing training and research center

Plans a multi-phase, $100 million expansion, adding biologics drug substance manufacturing capabilities