Agency for medicinal products and medical devices

Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and. Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and associated . INTRODUCTION. Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and. Website provides publications, reports and news regarding the safe use of medicinal products, medical devices and homeopathic medicinal products. The Agency for medicinal products and medical devices of Bosnia and Herzegovina was established by the Act of medicinal products and medical devices (“Official Gazette of B-H, no/08”) as an authority in the area of medicinal products and medical devices used in medical practices in B-H. It started with its work on 01 May The Agency for medicinal products and medical devices of Bosnia and Herzegovina was established by the Act of medicinal products and medical devices (“Official Gazette of B-H, no/08”) as an authority in the area of medicinal products and medical devices used in medical practices in B-H. It started with its work on 01 May Contact persons: Alija Uzunović, Tatjana Ponorac + 65 + 61 Main switchboard, from h + 51 + 51 (telefax) Show. Telephones h, only in emergency cases which could cause a recall of medicinal product. Medical Products Agency (Läkemedelsverket, LV) The Medical Products Agency is the responsible for regulation and surveillance of the development, manufacturing and sale of . Agency for Medicinal Products and Medical Devices of the Republic of Slovenia is a regulatory agency of the Republic of Slovenia competent for medicinal products and medical devices. Website provides publications, reports and news regarding the safe use of medicinal products, medical devices and homeopathic medicinal products.

  • The Agency for medicinal products and medical devices of Bosnia and Herzegovina was established by the Act of medicinal products and medical devices (" Official Gazette of B-H, no/08 ") as an authority in the area of medicinal products and medical devices used in medical practices in B-H. It started with its work on 01 May
  • The Agency for medicinal products and medical devices of Bosnia and Herzegovina was established by the Act of medicinal products and medical devices (" Official Gazette of B-H, no/08 ") as an authority in the area of medicinal products and medical devices used in medical practices in B-H. It started with its work on 01 May HALMED - Agency for Medicinal Products and Medical Devices About HALMED Medicinal Products Medical Devices Distribution, Manufacturing and Inspection Pharmacovigilance News and Educations HALMED publishes the report Medicinal Product Utilisation in Croatia from to EMA issued a final guideline on quality documentation for medicinal products that include a medical device in July This clarifies expectations laid down in Directive /83/EC and . The Agency for Medicinal Products and Medical Devices of Bosnia and Herzegovina is devoted to protecting and promoting public health care and to establishing. Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and associated activities in the private and public sector. We follow the basic goal (vision) that JAZMP remains and further consolidate its position as a professional, efficient and internationally recognized agency. INTRODUCTION. Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and associated activities in the private and public sector. We follow the basic goal (vision) that JAZMP remains and further consolidate its position as a professional, efficient and internationally recognized agency. INTRODUCTION. Our primary mission is to protect public health through the regulation and supervision of medicinal products, medical devices, blood, tissues and cells and associated activities in the private and public sector. Oct 13,  · MEDDEV (Medical Devices) /3 Rev3 guideline for “Borderline products, drug-delivery products, and medical devices incorporating, by an integral part, an ancillary . 58/08") as an authority in the area of medicinal products and medical devices used in medical practices in B-H. It started with its work on 01 May Agency structure. Agency for medicinal products and medical devices of Bosnia and Herzegovina. The Agency was established on May the 1st last year, but. 2. The Agency for medicinal products and medical devices of Bosnia and Herzegovina was established by the Act of medicinal products and medical devices (“Official. The course will be held at the HALMED’s premises, Ksaverska cesta 4, and the exact date of the course will be determined when enough interested participants has gathered (the foreseen duration 6 school hours). Mar 24, · The Agency for Medicinal Products and Medical Devices (HALMED) is organising in Zagreb an educational course “Distribution and good practice in medical device distribution”. The course will be held at the HALMED’s premises, Ksaverska cesta 4, and the exact date of the course will be determined when enough interested participants has gathered (the foreseen duration 6 school hours). The Agency for Medicinal Products and Medical Devices (HALMED) is organising in Zagreb an educational course “Distribution and good practice in medical device distribution”. Medical Products Agency (Läkemedelsverket, LV) The Medical Products Agency is the responsible for regulation and surveillance of the development, manufacturing and sale of drugs and other medicinal products. The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel committees of the European Medicines Agency (EMA), among others. Medical Products Agency (Läkemedelsverket, LV) The Medical Products Agency is the responsible for regulation and surveillance of the development, manufacturing and sale of drugs and other medicinal products. EMA issued a final guideline on quality documentation for medicinal products that include a medical device in July This clarifies expectations laid down in Directive /83/EC and addresses obligations in the Medical Devices Regulation, in particular under Article The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) is an independent federal higher authority. Manufacturers must comply with the Regulation when placing new medical devices on the market. It repeals Directive 93/42/EEC on medical devices and the Directive 90//EEC on active implantable medical devices. The Medical Devices Regulation applies since 26 May , following a four-year transition period. What's newBack number Copyright (C) Pharmaceuticals and Medical Devices Agency, All Rights Reserved. The Agency was established on May the 1st last year, but before than Bosnia and Herzegovina had two entites institutions for medicines and medical devices. Regulation of activities. Veterinary medicines. About us. Home. Blood, tissues and cells. Human medicines. Inspection. Medical devices. Agency for Medicinal Products and Medical Devices of the Republic of Slovenia. Index of medicinal products for human use. find medicine. open section. National Database for Medical Devices. National Agency for Medicines and Medical Devices. Sponsorships - Medicines for human use. Direct healthcare professionals communications. SPECIAL SECTIONS. download list in Excel format. It is an independent regulatory body competent for medicinal products and medical devices in the fields of human medicine and veterinary medicine, its purpose. Croatia, Agency for medicinal products and medical devices of. bnw-akademie.de, Bulgarian Drug Agency / Institute for Conrol of Veterinary Medicinal Preparations.
  • JCN Shin-Kasumigaseki Building, Kasumigaseki, Chiyoda-ku, Tokyo Japan.
  • In accordance with the Act of 18 March on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (Journal of Laws , No 82, item , as amended), the statutory activities of the Office include three core areas: carrying out procedures and activities involving medicinal products for human use and. What's newBack number Copyright (C) Pharmaceuticals and Medical Devices Agency, All Rights Reserved. Agency for Medicinal Products and Medical Devices (HALMED), Croatia - FDA, Confidentiality Commitment The United States Food and Drug. In accordance with the Act of 18 March on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (Journal of Laws , No 82, item , as amended), the statutory activities of the Office include three core areas: – carrying out procedures and activities involving medicinal products for human use and. На 7-миот Конгрес на фармацијата со меѓународно учество кој се одржува во Охрид од октомври на свеченото отварање имаше обраќање и директорот на Агенцијата за лекови и медицинкси средства Мр. Important notifications – Medicines for human use Important notifications – Medical devices National Agency for Medicines and Medical Devices. Medical Products Agency (Läkemedelsverket, LV) The Medical Products Agency is the responsible for regulation and surveillance of the development, manufacturing and sale of drugs and other medicinal products. MD, Republica Moldova, Chişinău str. The Medicines and Medical Devices Agency is an administrative authority empowered to regulate and supervise medicines, pharmaceutical and medical devices. Korolenko 2/1 (+) 22 88 43 01 (+) 22 88 43 03; [email protected] Contact information. The BASG monitors - nationally and in concert with the European sister agencies - the medicinal products and medical devices already on the.