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European Medicines Agency Company Profile

02:08 EDT 18th June 2018 | BioPortfolio

European Medicines Agency (EMEA) is a decentralised body of the European Union with headquarters in London.ts main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. The EMEA coordinates the evaluation and supervision of medicinal products throughout the European Union. The Agency brings together the scientific resources of the 25 EU Member States in a network of 42 national competent authorities. It cooperates closely with international partners, reinforcing the EU contribution to global harmonisation.

Location

7 Westferry Circus | Canary Wharf
London
London
E14 4HB
United Kingdom

Contact

Phone: 44-20) 74 18 84 00
Fax: 44-20) 74 18 84 16
Email: info@emea.eu.int


News Articles [2377 Associated News Articles listed on BioPortfolio]

European Medicines Agency Accepts Filing For Amgen's EVENITY

NewsAmgen and UCB announced that the European Medicines Agency (EMA) has accepted the Marketing Authorization Application for EVENITY (romosozumab) for the treatment of osteoporosis in postmenopausal ...

News and press releases: European Medicines Agency welcomes new Head of Veterinary Medicines

Ivo Claassen joins the Agency as of 1 March

European Medicines Agency Validates Type II Variation for Merck's KEYTRUDA (pembrolizumab) in Combination with Pemetrexed (ALIMTA) and Platinum Chemotherapy as First-Line Therapy in Metastatic Nonsquamous NSCLC, Based on Phase 3 KEYNOTE-189 Trial

Merck (NYSE: MRK), known as MSD outside the United States and Canada, today announced that following validation by the European Medicines Agency (EMA), the centralized review process has begun for...

Six new therapies backed for EU approval

Six medicines have taken a big step towards European approval having been recommended by the European Medicines Agency’s Committee for Medicinal Products for Human Use.

Sanofi and partner seek European Medicines Agency review for sleep sickness product

PARIS (Reuters) - French healthcare group Sanofi, along with its business partner, has asked the European Medicines Agency (EMA) to review the fexinidazole product for the treatment of sleeping sickne...

Enpr─EMA workshop on 'holistic approach to paediatric research'.on June 7 & 8, 2018

The European Network of Paediatric Research at the European Medicines Agency (Enpr─EMA) will hold its tenth annual workshop on 7–8 June 2018 at the European Medicines Agency (EMA).

European drug agency wins victory over drug companies that wanted to withhold data

The European Medicines Agency (EMA) has won an important court ruling backing its policy of open data.In an eagerly awaited judgment, the European Court of Justice backed data transparency and...

European Medicines Agency to review Sanofi-Regeneron's Dupixent, Cemiplimab

PARIS (Reuters) - The European Medicines Agency (EMA) will review the Dupixent (dupilumab) and Cemiplimab products being developed by drugmakers Sanofi and Regeneron, the companies said on Tuesday. ...

Drugs and Medications [169 Associated Drugs and Medications listed on BioPortfolio]

Terbinafine hydrochloride [Aurobindo Pharma Limited]

These highlights do not include all the information needed to use terbinafine hydrochloride safely and effectively. See full prescribing information for terbinafine hydrochloride tablets.Terbinafine H...

Cimetidine [Walgreen Company]

Walgreen Co. Cimetidine 200 Drug Facts

Dg health heartburn relief [Dolgencorp, LLC]

Dolgencorp, LLC Heartburn Relief Drug Facts

Acid reducer [Rite Aid Corporation]

Rite Aid Corporation Acid Reducer Drug Facts

Smart sense acid reducer [Kmart Corporation]

Kmart Corporation Acid Reducer Drug Facts

PubMed Articles [2124 Associated PubMed Articles listed on BioPortfolio]

Re: Availability of Evidence of Benefits on Overall Survival and Quality of Life of Cancer Drugs Approved by European Medicines Agency: Retrospective Cohort Study of Drug Approvals 2009-2013.

Effect of European Medicines Agency's regulatory measures on nimesulide utilization in Portugal.

What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU: A Brief Comparison of New Medicines Approved in Japan and the EU in 2016.

The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan and the European Medicines Agency (EMA) have a long-standing experience of reviews of new medicines, and they meet their target pre-marke...

Quantitative evaluation of the matrix effect in bioanalytical methods based on LC-MS: A comparison of two approaches.

Liquid chromatography coupled to mass spectrometry (LC-MS) is a powerful tool for studying pharmacokinetics and toxicokinetics. Reliable bioanalysis requires the characterization of the matrix effect,...

Postmarketing studies for novel drugs approved by both the FDA and EMA between 2005 and 2010: a cross-sectional study.

To characterise postmarketing studies for drugs that were newly approved by the US Food and Drug Administration and the European Medicines Agency.

Clinical Trials [1134 Associated Clinical Trials listed on BioPortfolio]

PENTA Fosamprenavir Study

Twice daily fosamprenavir, in combination with low dose ritonavir (FPV/RTV BID), is indicated for the treatment of HIV-infected adults, adolescents and children of 6 years of age and above...

Study of Talimogene Laherparepvec in Pancreatic Cancer

The purpose of this study is to find out which doses of talimogene laherparepvec (T-Vec) can be given safely to participants with pancreatic cancer that is either too big to be taken out b...

A Randomized Acceptability and Safety Study of the Transfer From Subutex to Suboxone in Opioid- Dependent Subjects (Study P04843)(COMPLETED)

Post-marketing commitment to the European Medicines Agency to conduct a prospective, controlled study of the transfer from Subutex to Suboxone.

A Non-interventional Study to Identify the Patients With Severe Luteinizing Hormone Deficiency in the Daily Practice

This non-interventional study is planned to identify the subjects with severe luteinizing hormone (LH) deficiency in the daily practice. The results will be used for the "Periodic Safety U...

Study of GSK Biologicals' Pandemic Influenza (H1N1) Candidate Vaccine in Children Aged 10 to Less Than 18 Years

The purpose of this study is to show that vaccination with a single dose of GSK Biologicals' pandemic H1N1 vaccine results in an immune response that meets or exceeds European Medicines Ag...

Companies [1572 Associated Companies listed on BioPortfolio]

European Medicines Agency

European Medicines Agency (EMEA) is a decentralised body of the European Union with headquarters in London.ts main responsibility is the protection and promotion of public and animal health, through t...

European Medicines Evaluation Agency (EMEA)

European Medicines Evaluation Agency (EMEA)

European Generic medicines Association

The EGA is the official representative body of the European generic pharmaceutical industry, which is at the forefront of providing high-quality affordable medicines to millions of Europeans and stimu...

European Directorate for the Quality of Medicines

The EDQM was created in 1996 and is a Directorate of the Council of Europe. Its premises have been especially designed for its various activities. Today the EDQM is organised into nine administrative...

Australia New ZealandTherapeutic ProductsAuthority

The trans Tasman therapeutic products agency project has involved New Zealand and Australia giving consideration to establishing a joint agency to regulate therapeutic products (medicines, medical dev...

More Information about "European Medicines Agency" on BioPortfolio

We have published hundreds of European Medicines Agency news stories on BioPortfolio along with dozens of European Medicines Agency Clinical Trials and PubMed Articles about European Medicines Agency for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of European Medicines Agency Companies in our database. You can also find out about relevant European Medicines Agency Drugs and Medications on this site too.

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