Danish product register
WebWho/what is the Product Register? The Product Register contains information on around 38,000 products on the market in Denmark and provides an overview which the Danish … WebJul 1, 2011 · The Danish National Prescription Registry contains data on all filled prescriptions at community pharmacies from 1995 and onwards (including dose, volume, …
Danish product register
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WebFeb 1, 2024 · The product can obtain CE marking after that. Incident reporting Manufacturers are obliged to notify the authorities of any serious incidents and field safety corrective actions of a medical device. Serious incidents occurring in Denmark must be reported to the Danish Medicines Agency. WebDec 13, 2024 · Product numbers; Central Reimbursement Register; Reimbursable nutritional products; Publications
WebRegister your product ; Authorized service providers ; Check repair status ; Training & certification ; Fraud alert ; Security Center WebInformation on the composition of about 30,000 chemical products was computerized. The possibilities and limitations of the use of a national data base on chemical products are …
WebOct 19, 2024 · The following entities must register with the DKMA if they are headquartered in Denmark: Manufacturers of medical devices in classes I, IIa, IIb and III, active implantable medical devices, custom made devices, and system and medical treatment packages (and Danish representatives of non-EU manufacturers), WebSep 9, 2024 · Act No. 3 of 3 January 2024 – The Danish Product Safety Act Executive Orders and EU Commission Regulations The Ministry of Health's Executive Order No. 1263 of 15 December 2008 concerning medical devices The Ministry of the Interior and Health's Executive Order No. 1269 of 12 December 2005 concerning in vitro diagnostic medical …
WebNational health registers. The Danish Health Data Authority is responsible for the national health registers that contain data related to the health of the entire Danish population …
WebMar 5, 2024 · The Danish product liability rules are well developed, well established and complicated. Denmark has a two-branch system where liability for damage or injury caused by a defective product may... indiana medical history museumhttp://danish.com/ indiana medicare phone numberWebIntroduction: Individual-level data on all prescription drugs sold in Danish community pharmacies has since 1994 been recorded in the Register of Medicinal Products Statistics of the Danish Medicines Agency. Content: The register subset, termed the Danish National Prescription Registry (DNPR), contains information on dispensed … indiana med lic lookupWebIn Denmark the Danish Environmental Protection Agency (EPA) is the Competent Authority Introduction to the new aspects of BPR Authorisation of biocidal products (including information on fees) Approval of active … indiana medical waste servicesWebProduct registration. Find the product you want to register * required. Country/Region * I primarily read in * I primarily use HP products and services for * Product Name or … indiana medicare part b fee scheduleWebJul 13, 2015 · Updated 03 March 2016 Companies can apply for authorisation to market medicines in Denmark and the EU/EEA in four different ways. The centralised procedure The centralised procedure in which new and high-technology medicines are authorised in the entire EU simultaneously. The European Medicines Agency (EMA) is responsible for … indiana medicare prior authorization formsWebThe Product Registry must be notified of a chemical product when it: is hazardous, typically when labelled with a hazard symbol. will be used professionally in Denmark. is … indiana medicare official website