This page shows the latest CMA news and features for those working in and with pharma, biotech and healthcare.
Pfizer and BioNTech’s jointly developed Omicron BA.4/BA.5 bivalent COVID-19 booster, Comirnaty Original/Omicron BA.4/BA.5, has been recommended for conditional marketing authorisation (CMA) by
Previously, Vaxzevria was given a conditional Marketing Authorisation (cMA) due to the critical nature of the COVID-19 pandemic, and as further significant evidence of safety and efficacy benefits of Vaxzevria
marketing authorisation (CMA) in the EU.
Novartis’ Pluvicto (INN: lutetium (177Lu) vipivotide tetraxetan) has been recommended for conditional marketing authorisation (CMA) in the EU for the treatment of adult patients with progressive prostate-specific membrane antigen
CLL accounts for around one-quarter of new leukaemia cases. BeiGene’s Brukinsa (zanubrutinib) has been recommended for conditional marketing authorisation (CMA) by the European Medicines Agency’s (EMA) Committee for
AstraZeneca (AZ) and Sanofi’s Beyfortus (nirsevimab) has been recommended for conditional marketing authorisation (CMA) in the EU for the prevention of respiratory syncytial virus (RSV) lower respiratory tract disease in
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A firm pharma focus. The CMA’s focus on the pharmaceutical industry is not surprising. ... cartel activities and serious abuses of a dominant position, which the CMA categorises.
The Advertising Standards Authority (ASA) and Competitions and Markets Authority (CMA) have been applying stricter guidelines and monitoring the industry more closely. ... Always seek advice from the agency you’re working with or directly from the ASA
The use of real-world evidence (RWE) as a complement to clinical trial data to support reimbursement decisions after Conditional Marketing Authorisation (CMA) is granted.
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Kardex is a global industry partner for intralogistics solutions and a leading supplier of automated storage solutions and material handling...