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Found 1176 results for any of the keywords spl spm. Time 0.021 seconds.
Structured Product Labeling, Structure Product Monograph SoftwareFreyr SPL/SPM is cloud hosted and On-premise software that supports in electronic drug registration listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
Regulatory Affairs, Operations, Intelligence, Case StudiesFreyr s case studies on Regulatory Affaris and Operations, Regulatory intelligence, Submission and Publishing to FDA
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.
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
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 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.
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.
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
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
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
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