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Found 17 results for the keyword ukrp. Time 0.005 seconds.
UK Responsible Person Services for Medical Device ManufacturersFreyr provides UK Responsible Person (UKRP) services to foreign medical device manufacturers for product registration and market entry in the UK.
What is Medical Device Ordinance (MedDO)?The Medical Device Ordinance (MedDO) is a set of regulations applicable for the medical devices to be marketed in Switzerland align with the EU Medical Device Regulation (EU) 2017/745.
Obligations for Economic Operators EOs | Freyr - Global Regulatory SolIn June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
Regulatory Labeling | Freyr - Global Regulatory Solutions and ServicesIn June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
Regulatory Affairs, Operations, Intelligence, Case StudiesFreyr s case studies on Regulatory Affaris and Operations, Regulatory intelligence, Submission and Publishing to FDA
Swixit and Its Impact on the MedTech IndustryThis article talks about the Swixit and its impact on the MedTech Industry and transitional timelines for various device categories.
Terms of UseIn June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
Fryer’s Cookie Policy | Freyr - Global Regulatory Solutions and ServicIntroduction: At Freyr Solutions, we are dedicated to delivering an exceptional user experience on our website. To accomplish this, we rely on the use of cookies, which are tiny text files that are stored on your device
Swixit - Regulatory Impact for Medical Devices Med Tech IndustryWe are delighted to see your interest in Freyr’s Webinar Series (FWS). The webinar on “Swixit - Regulatory Impact for Medical Devices Med Tech Industry” was successfully concluded on March 23, 2022. Here is an archived
Swissmedic s New Medical Device RegulationsThis article talks about the Swissmedic’s new medical device regulations for manufacturers to successfully market their products in Switzerland.
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