Use of big data to improve human and animal health
Together with the heads of the national competent authorities in the European Economic Area (EEA), known as Heads of Medicines Agencies (HMA), the European Medicines Agency (EMA) has established a new task force to explore how medicines regulators in the EEA can use big data to support research, innovation and robust medicines development in order to benefit human and animal health.
New portal “Information System for the Assessment of the Health Technologies – SIATS”
As from today, 23rd March, the new SIATS (Information System for the Assessment of the Health Technologies) portal is available, which will allow the MA holders and their representatives to manage the medicinal products accessibility.
Annex 16 QP Certification: important Questions and Answers
What can a Supply Chain Diagram look like? How to rely on vendor-supplied samples? These are just two examples of questions being frequently asked in connection with the new Annex 16 of the EU-GMP Guidelines (Certification by a Qualified Person and Batch Release).
Agenda - CHMP agenda of the 20-23 March 2017
Draft agenda for the meeting on 20-23 March 2017