Johnson & Johnson announced the submission of regulatory applications to the U.S. FDA and European Medicines Agency seeking approval of a ...

The global periodontal disease treatment market is projected to reach USD 3.63 billion by 2030 from USD 2.58 billion in 2024, ...

Rolling Submission of NDA for Aficamten Completed and Submitted to FDA in Q3COMET-HF, Confirmatory Phase 3 Clinical Trial of Omecamtiv ...

Directive Might Cause Massive Medicine Shortages Affecting Millions Of Patients Across Europe ...

FDA regulations categorize medical devices into three classes, with varying levels of control to manage risks and ensure the safety of medical technologies.

Francis Ford Coppola‘s Megalopolis has landed its latest international deal with Studiocanal taking European TV and streaming rights. The deal runs for seven years and excludes Spain ...

The world is facing two immediate health crises concerning drugs and vaccines: affordable and reliable access to life-sparing medicines and the safety and reliability of those medicines.

Medicines may be processed, packaged, sold, and resold multiple times before reaching consumers. For regulators, it can be difficult to ensure the safety of drugs before they hit pharmacy shelves.

The Eu­ro­pean Com­mis­sion said Fri­day that it has of­fi­cial­ly adopt­ed a new reg­u­la­tion ex­plain­ing how it will co­op­er­ate more close­ly with the Eu­ro­pean Med­i ...

Astellas Pharma Ltd. today announced that the Medicines and Healthcare products Regulatory Agency (MHRA ... Results were presented at the 2023 European Society for Medical Oncology (ESMO) Congress ...

Bayer BAYRY announced that it has submitted a marketing authorization application (MAA) to the European Medicines Agency ...