Germany Regulatory Health Authority

Listing Websites about Germany Regulatory Health Authority

Federal Institute for Drugs and Medical Devices - Wikipedia

(5 days ago) People also askWas ist GHA - German Health Alliance?Die GHA - German Health Alliance ist Partner der Geschäftsanbahnungsreise. Grateful for the insightful discussions and enriching exchanges at the 16th Health in Eastern Europe & Central Asia Meeting Ost-Ausschuss der Deutschen Wirtschaft / GHA - German Health Alliance held on Thursday, March 21, 2024.GHA – German Health Alliancegha.healthWho are the stakeholders in Germany's healthcare system?The report captures the broad spectrum of the German healthcare system’s stakeholders: hospitals, outpatient physicians, telemedicine providers, pharmacies, health insurers, patients, and insured citizens.Germany’s e-health transformation makes uneven progressmckinsey.comWhat is GHA - German Health Alliance / Alexander Boxler doing?GHA - German Health Alliance / Alexander Boxler provided an overview of the healthcare market in #Germany and highlighted the international presence of German companies. 2) Technical Visit to the London Institute for Healthcare Engineering. Intensive B2B Sessions. Technical Visit to the Kadans London Innovation Centre.GHA – German Health Alliancegha.healthWhat is regulatory and start-up guideline for clinical trials Germany?Regulatory and Start-up Guideline for Clinical Trials Germany v1.0_Okt 2019 1 Regulatory and Start-up Guideline for Clinical Trials Germany 1. Definitions 2. The Application 2a. National Competent Authorities 2b. Ethics Committee assessment 3. Time to get the approval 4. Costs to get the approval 5. General notification requirement 6.Regulatory and Start-up Guideline for Clinical Trialsgermannetpaet.deFeedbackBfArM - Bundesinstitut für Arzneimittel und Medizinproduktehttps://www.bfarm.de/ENBfArM - HomepageWEBThe Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) is an independent federal higher authority within the portfolio …

https://en.wikipedia.org/wiki/Federal_Institute_for_Drugs_and_Medical_Devices#:~:text=The%20Federal%20Institute%20for%20Drugs%20and%20Medical%20Devices,in%20Bonn%2C%20Germany.%20Its%20president%20is%20Karl%20Broich.

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Federal Institute for Drugs and Medical Devices - Wikipedia

(7 days ago) The Federal Institute for Drugs and Medical Devices (in German: Bundesinstitut für Arzneimittel und Medizinprodukte – BfArM) is the medical regulatory body in Germany. It operates under the Federal Ministry of Health (BMG). It is headquartered in Bonn, Germany. Its president is Karl Broich.

https://en.wikipedia.org/wiki/Federal_Institute_for_Drugs_and_Medical_Devices

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Federal Institute for Drugs and Medical Devices - GHPP: Global …

(3 days ago) WEBThe Federal Institute for Drugs and Medical Devices (BfArM) is an independent federal higher authority within the portfolio of the Federal Ministry of …

https://ghpp.de/en/institutes/bundesinstitut-fuer-arzneimittel-und-medizinprodukte/

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Homepage [www.zlg.de]

(2 days ago) WEBCentral Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices. Bodies. Notified Bodies. Contact. Do you have questions? Heinrich …

https://www.zlg.de/en/

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Federal Institute for Drugs and Medical Devices (BfArM)

(7 days ago) WEBThe Federal Institute for Drugs and Medical Devices is an independent specialised federal higher authority within the portfolio of the Federal Ministry of Health. Roughly 1,000 …

https://www.bundesgesundheitsministerium.de/en/en/ministry/authorities-within-the-remit/federal-institute-for-drugs-and-medical-devices-b

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The Federal Ministry of Health - Bundesgesundheitsministerium …

(7 days ago) WEBThe Federal Ministry of Health is responsible for a variety of policy areas, whereby its activities focus predominantly on the drafting of bills, ordinances and …

https://www.bundesgesundheitsministerium.de/en/ministry/the-federal-ministry-of-health/

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Federal Ministry of Health

(7 days ago) WEBVaccinations are among the most important and effective means of preventing disease. Overview of all recommended vaccinations and more. If we achieve a breakthrough in digitalisation, it will change practical …

https://www.bundesgesundheitsministerium.de/en/index.html

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Regulation - Paul-Ehrlich-Institut - PEI

(3 days ago) WEBRegulation. Regulation. Navigation. Advice; Clinical Trials; Marketing Authorisation (Human) Marketing Authorisation (Veterinary) Approvals; The Paul-Ehrlich-Institut is an Agency of the German Federal Ministry of …

https://www.pei.de/EN/regulation/regulation-node.html

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Homepage European Medicines Agency

(7 days ago) WEBThe European Medicines Agency's (EMA) office is closed from 18:00 on Tuesday 30 April 2024 to 07:30 on Thursday 2 May 2024. Outside of working hours and on public …

https://www.ema.europa.eu/en/homepage

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Homepage - Paul-Ehrlich-Institut - PEI

(1 days ago) WEBCurrent regulatory highlights on vaccines and biomedicines including recommendations for marketing authorisation and indication extensions – April 2024. Pagination. Global …

https://www.pei.de/EN/home/home-node.html

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Germany’s e-health transformation makes uneven progress

(5 days ago) WEBDiGA, a new regulatory and reimbursement pathway for digital health applications. From June 2020 to November 2021, 104 DiGAs have been submitted for …

https://www.mckinsey.com/industries/life-sciences/our-insights/germanys-ehealth-transformation-makes-good-but-uneven-progress

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Institute - Paul-Ehrlich-Institut - PEI

(1 days ago) WEBWelcome. The Paul-Ehrlich-Institut (PEI), the Federal Institute for Vaccines and Biomedicines, in Langen near Frankfurt/Main is a senior federal authority reporting …

https://www.pei.de/EN/institute/institute-node.html

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RKI - Standing Committee on Vaccination

(4 days ago) WEBSTIKO. ) In Germany, the Standing Committee on Vaccination (STIKO) develops national recommendations for the use of licensed vaccines. The STIKO …

https://www.rki.de/EN/Content/infections/Vaccination/Vaccination_node.html

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Regulatory and Start-up Guideline for Clinical Trials Germany

(9 days ago) WEBRegulatory and Start-up Guideline for Clinical Trials Germany v1.0_Okt 2019 14. 13.1.2.2.2 For submission of an integrated study protocol with additional sub-studies in accordance …

https://www.germannetpaet.de/fileadmin/Media/06_Material/Regulatory_and_Start-up_Guideline_Clinical_Trials_Germany_final_2019.pdf

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BfArM - Medical devices

(Just Now) WEBThe tasks of BfArM in the field of medical devices result in particular from the Medical Device Regulation ( MDR) ( EU) 2017/745, the Medical Device Law Implementation …

https://www.bfarm.de/EN/Medical-devices/_node.html

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GHA – German Health Alliance

(2 days ago) WEBGHA – German Health Alliance – successful trade fair presence at MEDICA 2023 October 24, 2023 6th German – Eastern European & Central Asian Health Forum: Investments …

https://gha.health/en/

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BfArM - Medicinal products information

(7 days ago) WEBThe BfArM provides information on medicinal products for healthcare professionals and consumers. The Public Assessement Reports state the background for scientific …

https://www.bfarm.de/EN/Medicinal-products/Information-on-medicinal-products/_node.html

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About Escherichia coli Infection E. coli infection CDC

(2 days ago) WEBOverview. E. coli are germs called bacteria.They are found in many places, including in the environment, foods, water, and the intestines of people and animals. …

https://www.cdc.gov/ecoli/about/index.html

Category: Food Show Health

BfArM - Clinical trials

(9 days ago) WEBClinical Trials Information System - CTIS Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for …

https://www.bfarm.de/EN/Medicinal-products/Clinical-trials/_node.html

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