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- https://www.ch-repservices.com/regulation-changesWWW.CH-REPSERVICES.COMSwiss medical device regulations, Swiss AR services, CH-REP, MedDO, ClinDOFreyr provides Swiss Authorized Representative(CH-REP) services for medical device manufacturers outside the Switzerland as per Swissmedic regulations.0 Yorumlar 0 hisse senetleri 236 Views 0 önizleme
- https://www.ukrpservices.com/regulation-changesWWW.UKRPSERVICES.COMUKRP services, MHRA requirements, MHRA medical device registrationFreyr provides United Kingdom Responsible Person(UKRP) services for medical device manufacturers outside the UK as per MHRA regulations.0 Yorumlar 0 hisse senetleri 230 Views 0 önizleme
- https://medicaldevices.freyrsolutions.com/de-novo-registration-of-medical-devicesMEDICALDEVICES.FREYRSOLUTIONS.COMDe Novo Registration, FDA Medical Device ClassificationFreyr provides regulatory support to the medical device manufacturers in De-Novo registration of medical devices in the USA that span across classification, Pre-Submission/Q-Submission meeting request, risk benefit determination, De-Novo submission package compilation, publishing and creation for Pre-Submissions.0 Yorumlar 0 hisse senetleri 346 Views 0 önizleme
- https://www.ch-repservices.com/freyr-ch-rep-servicesWWW.CH-REPSERVICES.COMSwiss Authorized Representative, CH-REP services, Swiss distributorFreyr provides Swiss Authorized Representative(CH-REP) services for foreign medical device manufacturers and acts as Swiss distributor/importer of devices across Switzerland.0 Yorumlar 0 hisse senetleri 229 Views 0 önizleme
- https://www.ch-repservices.com/impact-on-medical-devices-marketWWW.CH-REPSERVICES.COMSwiss Authorized Representative(CH-REP), CE mark medical device labeling requirementsFreyr provides Swiss Authorized Representative(CH-REP) services for medical devices and IVD manufacturers in CE marking and labeling support as per Swissmedic regulations.0 Yorumlar 0 hisse senetleri 237 Views 0 önizleme
- https://www.ukrpservices.com/impact-on-medical-devices-marketWWW.UKRPSERVICES.COMUK responsible person services, UKCA marking, UKNI mark, UK CE markFreyr provides United Kingdom Responsible Person(UKRP) services for medical devices and IVD manufacturers that span across registration, UKCA marking, UK CE marking, UKNI marking and labeling support as per MHRA regulations.0 Yorumlar 0 hisse senetleri 233 Views 0 önizleme
- https://www.ukrpservices.com/freyr-servicesWWW.UKRPSERVICES.COMUK responsible person service, UK Distributor | Freyr UKRP ServicesFreyr provides United Kingdom Responsible Person(UKRP) services for foreign medical device manufacturers with end-to-end regulatory support for registration and market entry in UK.0 Yorumlar 0 hisse senetleri 237 Views 0 önizleme
- https://medicaldevices.freyrsolutions.com/513g-submissionMEDICALDEVICES.FREYRSOLUTIONS.COM513(g) Submission, medical device classification, CDRH, USFDAFreyr provides regulatory support for medical device manufacturers in 513 g submission, which includes medical device classification, preparation & review of 513g application and interaction with agency to comply with CDRH, FDA.0 Yorumlar 0 hisse senetleri 333 Views 0 önizleme
- https://medicaldevices.freyrsolutions.com/510k-premarket-notificationMEDICALDEVICES.FREYRSOLUTIONS.COM510k Premarket Notification, 510 k submission, 510K application, USFDAFreyr provides regulatory support for medical device manufacturers in 510k submission (510 k premarket notification) to USFDA, which include predicate device identification, 510k application compilation, gap analysis, publishing, creation & validation of e-copy, device listing for compliant market entry0 Yorumlar 0 hisse senetleri 326 Views 0 önizleme
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