What does EMEA mean in PRESCRIPTION
The European Medicines Evaluation Agency (EMEA) is a regulatory agency that evaluates and monitors the efficacy, safety, and quality of medicines for human use in Europe. It acts as an interface between the European Union (EU) and its Member States, pharmaceutical industry, health professionals, patients and general public.
EMEA meaning in Prescription in Medical
EMEA mostly used in an acronym Prescription in Category Medical that means European Medicines Evaluation Agency
Shorthand: EMEA,
Full Form: European Medicines Evaluation Agency
For more information of "European Medicines Evaluation Agency", see the section below.
» Medical » Prescription
Essential Questions and Answers on European Medicines Evaluation Agency in "MEDICAL»PRESCRIPTION"
What is EMEA?
The European Medicines Evaluation Agency (EMEA) is a regulatory agency that evaluates and monitors the efficacy, safety, and quality of medicines for human use in Europe.
What does EMEA do?
EMEA's primary function is to provide scientific advice to pharmaceutical companies seeking authorization to market their medicinal products in Europe. It also undertakes pharmacovigilance activities to monitor the safety of medicinal products during their life cycle; provides opinions on studies and clinical trials; reviews veterinary medicines; coordinates the development of common guidelines among EU member states; assesses orphan drugs; investigates counterfeit medicines; provides educational resources for healthcare professionals and consumers; and advocates good practices.
Who does EMEA serve?
EMEA serves as an interface between the European Union (EU) and its Member States, pharmaceutical industry, health professionals, patients and general public.
How does EMEA evaluate medicines?
As part of its review process for new medicinal products, EMEA experts evaluate data from clinical trials conducted in humans with respect to efficacy, safety and quality of medicinal products before they can be authorised. The experts also assess non-clinical data such as pharmacology or toxicology data related to each medicine.
Does EMEA also evaluate veterinary medicines?
Yes, as part of its mandate to actively promote animal health in Europe, EMEA also coordinates the authorisation procedure for certain veterinary medicinal products within the EU
Final Words:
Established in 1995 after two decades of research into how best to regulate medicinal products at a regional level in Europe, the European Medicines Evaluation Agency has become one of the most important organisations when it comes to regulating new medications throughout the continent. Its decisive role in ensuring only effective therapies are made available has helped millions of Europeans access reliable prescriptions safely over more than two decades since its inception.
EMEA also stands for: |
|
| All stands for EMEA |