freyrregintel logo Meet Freya
close

The European Commission has initiated a public consultation regarding the draft implementing act for joint scientific consultations on human medicines under Regulation (EU) 2021/2282 on Health Technology Assessment (HTA). Stakeholders have until October 29th to submit their input on the detailed procedural rules outlined in the draft. This consultation seeks to gather pertinent information for implementing the Regulation on Health Technology Assessment, focusing on the submission of requests by developers, stakeholder selection and consultation, and collaboration with the European Medicines 

Source: https://www.aemps.gob.es/informa/la-ce-lanza-una-consulta-publica-sobre-el-acto-de-ejecucion-de-consultas-cientificas-conjuntas-de-medicamentos-de-uso-humano/

Region: Spain

Related Regulatory News and Updates

blog-thmbnail

Mandatory Requirements for an Effective Over-the-counter Medicines Application

November, 2024
blog-thmbnail

Announcement to Product Registration Holders (PRHs): Pilot Project for Post-Approval Changes (Variation) Using Reliance

November, 2024
blog-thmbnail

Patient-Focused Drug Development: Workshop to Discuss Methodologic and Other Challenges Related to Patient Experience Data; Public Workshop; Request for Comments

November, 2024
blog-thmbnail

Guidance Providing an Overview of Listed Medicines and Listed Assessed Medicines Pathways and Legislative Requirements: Understanding the Legislative Framework for Listed Medicines

November, 2024
pattern
pattern
Got questions? We’ve got answers!

Let's talk Regulatory!

Reach out to us and let’s unravel your Regulatory puzzle together. Unlock regulatory solutions with our global subject matter experts and tap into a wealth of regulatory intelligence.

Speak to an Expert