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BioPharma

Key Steps For Biopharma Startups Getting Ready For EU HTA

What is the Joint European HTA? Navigating pricing and reimbursement in the European Union (EU) can be a complex task for emerging biopharmaceutical companies (EBPs),...

Elevating Biopharmaceutical Projects With The Right CDMO

In the biopharma industry, selecting the right contract development and manufacturing organization (CDMO) is pivotal to a successful pharmaceutical development journey. This decision hinges...

Overcoming Challenges In Biopharma Novel Drug Manufacturing

The biopharmaceutical sector is undergoing a significant transformation in treating complex diseases, especially in oncology, driven by innovative drug approaches. This shift entails personalized...

Enhanced Biopharmaceutical Release: Autonomous PAT Power

Speeding up biomanufacturing using automated Process Analytical Technology (PAT) systems A2P2 and Micro Sequential Injection (SI), two cutting-edge process analysers, have been cited as autonomous...

Overcoming Treatment Challenges With Cell And Gene Therapies

Gene and cell therapies have the potential to revolutionize healthcare by reprogramming the immune system to treat diseases that are difficult to address with...

Boosting Innovation And Value In UK Biopharma And Medtech

New recommendations from Imperial College London aim to boost competitiveness in the UK's biopharma and Medtech sectors. It assesses the value-added per capita in...

Cell And Gene Therapy CDMO Services Market Is On The Rise

The global cell and gene therapy Contract Development and Manufacturing Organization (CDMO) services market, which was valued at USD 5,193.7 million in 2022, is...

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