medical drugs protection device Germany

  • Q A pharma medical device regulation in GermanyLexology

    Dec 10 2019  A Q A guide to pharma medical device regulation in Germany covering the healthcare bodies and competent authorities marketing authorisation defective and

  • Healthcare Resource Guide GermanyExport.govHome

    The German market for medical devices is regulated by German and EU directives standards and safety regulations. The EU Medical Device Regulation MDR will take effect on May 26 2020 with increased testing certification and compliance requirements. The complementary IVD Regulation will come into effect in May 2022.

  • Your Medical Device Consulting GroupMDR Competence

    The new Medical Devices Regulation MDR On April 5. 2017 the EU Parliament adopted the new Medical Devices Regulation MDR . The scheme entered into force on May 25. 2017. The Federal Association of Medical Technology Companies in Germany BVMed immediately called for a german „national support program for MedTech SMEs .

  • Drug and Medical Device Reimbursement Consultants

    What makes us better We’ve successfully guided hundreds of life science clients from around the world in commercializing their medical devices drugs and apps. We cover 15 countries see below with our team of local experts assembled according to each clients’ selected target markets and phase within the reimbursement process.

  • BfArMAbout us

    About us. The Federal Institute for Drugs and Medical Devices Bundesinstitut für Arzneimittel und Medizinprodukte BfArM is an independent federal higher authority within the portfolio of the Federal Ministry of Health. At the BfArM roughly 1 250 employees physicians pharmacists chemists biologists lawyers engineers technical assistants administrative staff etc. are involved in

  • HomeMeds Disposal

    The different disposal routes for drugs and medicines in Germany are environmentally conscious and safe. As general waste is incinerated in most parts of Germany >80 disposal of unused or expired medicine through general waste is in most areas the safest and recommended route.

  • Federal Institute for Drugs and Medical Devices BfArM

    May 26 2020  The Federal Institute for Drugs and Medical Devices BfArM office Cologne emerged from the German Institute of Medical Documentation and Information DIMDI which was incorporated into BfArM on 26 May 2020.The institute provides high quality information for all areas of the health system via Internet.


    These clients benefit from our experience that we gained from supporting hundreds of different molecules in preclinical development. Our experience includes food additives small molecules and biotechnology derived drugs vaccines medical devices and drug device combinations all developed in a broad range of clinical indications.

  • Guide to Health Insurance and Healthcare System in Germany

    Aug 20 2020  Germany’s healthcare contribution costs are 14.6 to 15.6 half of which the worker pays and half the employer. There may also be a small supplemental rate on top of this at an average of 0.9 which is paid solely by the employee. This supplement is a contribution rate charged by the state German health insurer.

  • Medical Röchling EN

    Röchling Medical The Medical division offers customers a wide range of high quality customized components and assemblies right through to end to end OEM products. The product portfolio also includes standard plastic products with special expertise in the fields of diagnostics fluid management pharma surgery and interventional and much more.

  • Global Regulatory Authority Websites

    Germany Ministry of Health Germany Federal Institute for Drugs and Medical Devices Germany Robert Koch Institute in German Germany Paul Ehrlich Institute in German Germany Federal Institute for Risk Assessment in German Germany Ministry of Consumer Protection Food and Agriculture in German

  • Federal Institute for Drugs and Medical DevicesWikipedia

    The Federal Institute for Drugs and Medical Devices in German Bundesinstitut für Arzneimittel und MedizinprodukteBfArM is the medical regulatory body in Germany operates under the Federal Ministry of Health BMG . It is headquartered in Bonn Germany. Its president is Prof. Dr. Karl Broich.

  • Clinical trials in GermanyLexology

    Dec 19 2018  The applicant or its legal representative with a permanent place of business in the European Economic Area submits a formal application to Federal Institute for Drugs and Medical Devices BfArM

  • About the German Medical Association

    The German Medical Association Bundesärztekammer is the central organisation in the system of medical self administration in Germany. As the joint association of the State Chambers of Physicians Landesärztekammer it represents the interests of 506 014 physicians status 31/12/2017 in matters relating to professional policy and plays an active role in opinion forming processes with

  • People taking anti inflammatory drug mount Medical News

    Jun 02 2021  People taking anti inflammatory drug mount a weaker immune response to COVID 19 vaccine. One quarter of people who take the drug methotrexate for common immune system disorders from rheumatoid

  • List of Foreign Countries or Regions and Their Regulatory

    State Institute for Drug Control Federal Republic of Germany Federal Ministry of Health Central Authority of the Länder for Health Protection regarding Medicinal Products and Medical Devices Hellenic Republic Greece Greek National Organisation for Medicines

  • The Reimbursement Environment for Medical Devices in France

    Jun 13 2018  USA IDR Medical North America 225 Franklin Street 26th Floor Boston Massachusetts 02110 USA T 1 0 617.275.4465

  • Customs onlineMedicinal products and narcotics

    Medicinal products and narcotics. To protect the public from health risks and to combat illegal drug trafficking in Germany the trade in medicinal products and narcotics is strictly regulated. Here you can find out what to bear in mind if you are in the possession of medicines when travelling.

  • Want to See the Future of Digital Health Tools Look to

    Dec 02 2020  The Fast Track Process is run by the Federal Institute for Drugs and Medical Devices Bundesinstitut für Arzneimittel und Medizinprodukte or BfArM which plays many of the same roles in Germany

  • COVID 19Legal Implications for Pharmaceutical and

    Apr 10 2020  The impact of Coronavirus COVID 19 on pharmaceutical and medical device companies has been unique as not only have these businesses had to set up emergency management systems practically overnight in order to maintain normal their business operations the population also expects the sector to make significant contributions to the fight against COVID 19.

  • Pharmaceutical medical device advertising regulation in

    In Germany the rules on advertising for medicines and medical devices are primarily enforced by civil courts. If a company allegedly violates a provision of the HWG such violation is at the same time an act of unfair competition.

  • MEDICA Trade FairMEDICA 2021– Top in all medical areas

    Delve into the world of medical technology The whole industry will meet at MEDICA in Düsseldorf from 1518 November 2021.Experience high tech products meet world market leaders hidden champions and start ups or visit the top class forums and conferences.

  • Medical Device Price Differentials In The U.S. And Europe

    Dec 07 2018  In this post we discuss reasons for medical device price differentials that might arise from countries’ diverging regulatory frameworks focusing especially on the case of drug eluting stents.

  • The Reimbursement Environment for Medical Devices in Germany

    May 02 2018  The reimbursement process in this environment is more complex. Medical practices receive funds from their Regional Association of Statutory Health Insurance Physicians GKV SV per quarter. There are 17 regional KVs Office physician association Kassenärztliche Vereinigung in Germany that are responsible for ensuring a sufficient level of care.

  • Welcome to Dräger USLeading Medical Safety Technology

    Alcohol And Drug Testing frequent questions and to show you product and application information about the usage and the reprocessing of Dräger medical devices and safety protection equipment. substances can’t be completely controlled respiratory protective equipment must be used. Dräger designs respiratory protection devices in

  • European Medical Devices MarketGlobal Forecast to 2025

    8 medical devices market by end user page no.78 8.1 introduction 8.2 hospitals and clinical care settings 8.3 home care settings . 9 medical devices market by region page no.81 9.1 introduction 9.2 germany 9.2.1 germany is the largest market for medical devices in europe 9.3 uk

  • The Top 15 Medical Device Companies in the World in 2020

    Johnson Johnson operates three distinct divisionsmedical devices pharmaceuticals and consumer health. Both their medical device and pharmaceutical divisions have manufacturing sites in Ireland. Johnson Johnson products are marketed in 57 countries via almost 250 operating companiesglobal personnel is approximately 132 200.

  • MedicalHenkel Adhesives

    For the medical electronic device industry Henkel offers high reliability proven assembly solutions like electrically conductive inks adhesives encapsulation underfill solder and film materials. Such solutions are used in the assembly of cardio neuro stimulation devices moisture detecting sensors ECG and TENS electrodes.

  • Germany bans export of medical protection gear due to

    Mar 04 2020  Germany has banned the export of medical protection gear to avoid supply shortages of masks gloves and suits as doctors and authorities are racing to

  • Preclinical and Clinical Trial Requirements Germany

    Jun 28 2019  Prepared in association with Heuking Kühn Lüer Wojtek a leading global law firm this is an extract from The Pharma Legal Handbook Germany available to purchase here for USD 99. 1. What is the authorization process for the marketing of new drugs biologics medical devices over the counter medications and other medicinal products 1.

  • List of national authorities for Medical Devices EU MDR

    Bulgarian Drug Agency Department Control of Medicinal Products and Medical devices 8 Damyan Gruev Str. 1303 Sofia Bulgaria. Tel 359 2 890 34 83Fax 359 2 890 34 34. e mail bda Website

  • ServiceDIMDI

    MedTech Europe represents manufacturers and associations in the field of medical devices troughout Europe. U.S. Food and Drug Administration FDA The FDA is an U.S. American organisation of public health working for consumer protection in the field of foods cosmetics drugs medical devices etc. Medical Device Reporting and Recall Reports are

  • Compression Devices Solutions Cardinal Health

    Compression Devices and Solutions. Smart Compression is the next evolution of IPC. It’s designed to move more blood 1 to help prevent stasis 1 track compliance 2 and educate patients and clinicians about the risk of VTE. All while thinking about the impact on the environment.

  • Safety informationInternational Medical Device

    United Kingdom. National Patient Safety Alerts. Alerts and recalls for drugs and medical devices. Alerts and recalls for drugs and medical devices153 alerts for Field safety notice. Medical devices regulation and safetyLatest documents. 5. Japan. Safety Information regarding Medical Devices. .

  • Medical devices European Medicines Agency

    A medical device may contain an ancillary medicinal substance to support the proper functioning of the device. These products fall under the medical devices legislation and must be CE marked. Examples of medical devices with an ancillary medicinal substance include drug eluting stents bone cement containing an antibiotic catheters coated with heparin or an antibiotic agent and condoms coated

  • BfSRadiation Protection Act

    May 12 2017  X ray mammography image Source Dr. med. H. Junkermann. In Germany mammography examination for the early diagnosis of breast cancer in women between age 50 and age 69 is currently the only screening examination for early diagnosis using X radiation. According to the new Radiation Protection Act it is also possible to approve individual early diagnosis measures in future.