https://www.meditrial.net/latest-news/ 2022-07-04T13:32:48+00:00 https://www.meditrial.net/2026/05/fda-breakthrough-device-acceleration/ 2026-06-16T12:50:41+00:00 https://www.meditrial.net/2020/03/zhejiang-university-handbook-of-covid-19-prevention-and-treatment/ 2024-02-29T17:19:53+00:00 https://www.meditrial.net/2020/06/usa-fda-updates-its-guidance-on-conduct-of-clinical-trials-of-medical-products-during-covid-19-emergency/ 2024-02-29T17:18:32+00:00 https://www.meditrial.net/2022/02/us-the-fda-has-finalized-guidance-on-the-use-of-premarket-pathways-for-combination-products-2/ 2024-02-29T17:17:22+00:00 https://www.meditrial.net/2020/06/usa-fda-issued-guidance-for-remote-patient-monitoring-devices-used-during-covid-19/ 2024-02-29T17:13:19+00:00 https://www.meditrial.net/2020/08/us-the-fda-answers-devices-importers-questions-during-covid-19/ 2024-02-29T17:10:45+00:00 https://www.meditrial.net/2020/09/us-fda-updates-the-guidance-on-the-conduct-of-clinical-trials-during-covid-19-pandemic/ 2024-02-29T17:09:11+00:00 https://www.meditrial.net/2021/01/us-fda-releases-artificial-intelligence-machine-learning-action-plan/ 2024-02-29T17:06:58+00:00 https://www.meditrial.net/2020/08/us-fda-publishes-user-fee-amounts-for-medical-device-manufacturers-in-2021/ 2024-02-29T17:06:35+00:00 https://www.meditrial.net/2020/06/us-fda-published-qa-guidance-on-the-effects-of-the-covid-19-emergency-on-formal-meetings-and-user-fee-applications-for-medical-devices/ 2024-02-29T17:05:07+00:00 https://www.meditrial.net/2020/06/us-fda-published-finalized-guidance-on-inspections-of-medical-device-establishments/ 2024-02-29T17:02:19+00:00 https://www.meditrial.net/2020/08/us-fda-issues-provides-specific-perfomance-criteria-for-cutaneous-electrodes-and-some-catheters/ 2024-02-29T16:58:13+00:00 https://www.meditrial.net/2021/03/us-fda-provides-examples-on-real-world-evidence-to-support-marketing-applications-for-medical-devices/ 2024-02-29T16:54:30+00:00 https://www.meditrial.net/2020/07/us-fda-plans-to-resume-on-site-domestic-inspections-as-of-20-july-2020/ 2024-02-29T16:53:39+00:00 https://www.meditrial.net/2020/10/us-fda-launches-the-digital-health-center-of-excellence/ 2024-02-29T16:51:55+00:00 https://www.meditrial.net/2020/09/us-fda-issues-guidance-on-iso-10993-1-for-the-biological-evaluation-of-medical-devices/ 2024-02-29T16:50:47+00:00 https://www.meditrial.net/2020/07/us-fda-issues-final-guidance-on-multiple-function-device-products/ 2024-02-29T16:48:12+00:00 https://www.meditrial.net/2020/10/us-fda-introduces-new-medical-device-development-tools-for-sponsors/ 2024-02-29T16:45:09+00:00 https://www.meditrial.net/2022/03/us-fda-guidance-on-center-for-devices-and-radiological-health-cdrh-appeals-processes/ 2024-02-29T16:44:37+00:00 https://www.meditrial.net/2020/07/us-fda-exempts-additional-class-ii-devices-from-510k-requirements/ 2024-02-29T16:40:22+00:00 https://www.meditrial.net/2020/09/us-fda-green-lights-the-path-for-epro-through-regulation/ 2024-02-29T16:38:59+00:00 https://www.meditrial.net/2020/03/us-fda-reactions-to-mitigate-pandemic-impact-on-industry-and-the-public/ 2024-02-29T16:35:19+00:00 https://www.meditrial.net/2021/05/mayday-mayday-upgrade-your-trials-for-mdr-by-may-26-2021/ 2024-02-29T16:33:44+00:00 https://www.meditrial.net/2020/06/uk-the-mhra-provides-regulatory-flexibilities-resulting-from-covid-19/ 2024-02-29T16:31:53+00:00 https://www.meditrial.net/2020/05/uk-mhra-update-regulatory-status-of-equipment-being-used-to-help-prevent-coronavirus-covid-19/ 2024-02-29T16:29:24+00:00 https://www.meditrial.net/2021/02/uk-mhra-updates-guidance-on-virtual-manufacturing-of-medical-devices/ 2024-02-29T16:27:55+00:00 https://www.meditrial.net/2020/11/uk-mhra-supports-generating-rwe-in-clinical-trials-through-digital-solutions/ 2024-02-29T16:25:13+00:00 https://www.meditrial.net/2022/02/uk-mhra-published-guidance-on-clinical-trial-risk-assessment-oversight-and-monitoring-activities/ 2024-02-29T16:24:13+00:00 https://www.meditrial.net/2020/06/uk-mhra-provides-regulatory-guidance-on-software-used-in-the-diagnosis-treatment-and-management-of-covid-19-patients/ 2024-02-29T16:23:25+00:00 https://www.meditrial.net/2020/04/uk-mhra-pragmatic-and-flexible-approach-allows-special-measures-for-clinical-research-under-covid-19/ 2024-02-29T16:18:52+00:00 https://www.meditrial.net/2020/08/uk-mhra-plans-to-restart-on-site-inspections-as-of-september-2020/ 2024-02-29T16:01:48+00:00 https://www.meditrial.net/2020/06/uk-mhra-launched-yellow-card-website-for-reporting-covid-19-related-issues/ 2024-02-29T15:25:55+00:00 https://www.meditrial.net/2020/06/uk-mhra-issued-a-guidance-on-the-3d-printing-of-medical-devices-or-component-parts-during-covid-19/ 2024-02-29T15:21:59+00:00 https://www.meditrial.net/2020/05/uk-mhra-advice-for-investigators-and-sponsors-of-ongoing-clinical-trials-and-new-applications/ 2024-02-29T15:19:51+00:00 https://www.meditrial.net/2020/05/uk-managing-clinical-trials-during-covid-19/ 2024-02-29T15:17:32+00:00 https://www.meditrial.net/2020/07/uk-changes-to-amendment-submission-to-hra-mrec/ 2024-02-29T15:14:45+00:00 https://www.meditrial.net/2020/11/uk-information-session-for-swiss-medtech-companies/ 2024-02-29T15:06:23+00:00 https://www.meditrial.net/2021/06/turkey-new-mdr-and-ivdr-are-applicable/ 2024-02-29T15:05:43+00:00 https://www.meditrial.net/2020/03/guideline/ 2024-02-29T15:05:31+00:00 https://www.meditrial.net/2020/07/the-usa-fda-is-holding-back-the-enforcement-of-certain-udi-requirements/ 2024-02-29T14:46:51+00:00 https://www.meditrial.net/2022/02/the-mdcg-updates-the-ivdr-implementation-and-preparation-plan-eu-2017-746-2/ 2024-02-29T14:43:15+00:00 https://www.meditrial.net/2020/10/the-international-medical-device-regulators-forum-imdrf-issued-an-update-on-pmcf-studies/ 2024-02-29T14:41:05+00:00 https://www.meditrial.net/2020/07/the-european-commission-updates-on-mdr-implementation/ 2024-02-29T14:40:29+00:00 https://www.meditrial.net/2020/05/the-european-commission-simplifies-the-process-for-renewing-notified-body-designations/ 2024-02-29T14:38:43+00:00 https://www.meditrial.net/2020/05/the-european-commission-answers-questions-about-covid-19-tracing-apps-across-the-eu/ 2024-02-29T14:36:51+00:00 https://www.meditrial.net/2022/04/the-eudamed-udi-devices-module-updated-technical-documentation-is-available/ 2024-02-29T14:33:14+00:00 https://www.meditrial.net/2021/03/switzerland-new-requirements-and-changes-to-authorization-practice-as-of-may-2021/ 2024-02-29T14:31:01+00:00 https://www.meditrial.net/2021/05/switzerland-new-regulations-applicable-to-medical-devices-as-of-26-may-2021/ 2024-02-29T14:30:34+00:00 https://www.meditrial.net/2020/03/switerland-new-ordinance-for-clinical-trials-during-covid-19-emergency/ 2024-02-29T14:29:45+00:00 https://www.meditrial.net/2020/04/switzerland-introduction-of-duty-free-import-for-medical-goods/ 2024-02-29T14:28:12+00:00 https://www.meditrial.net/2020/04/switzerland-exception-for-marketing-of-medical-devices-under-covid-19/ 2024-02-29T14:26:41+00:00 https://www.meditrial.net/2022/03/swiss-single-registration-number-chrn/ 2024-02-29T14:19:54+00:00 https://www.meditrial.net/2022/03/swiss-medical-device-database-is-under-construction/ 2024-02-29T14:19:37+00:00 https://www.meditrial.net/2020/06/spain-monitoring-visits-in-hospitals-allowed-again/ 2024-02-29T14:18:56+00:00 https://www.meditrial.net/2020/05/spain-exceptional-measures-for-clinical-trials-to-manage-problems-due-to-covid-19/ 2024-02-29T14:17:04+00:00 https://www.meditrial.net/2020/05/spain-gives-medtech-companies-another-11-months-to-adapt-to-brexit/ 2024-02-29T14:13:21+00:00 https://www.meditrial.net/2020/03/slovenia-jazmp-operates-smoothly-under-the-current-emergency/ 2024-02-29T14:12:25+00:00 https://www.meditrial.net/2020/03/slovakia-sukl-issues-guidance-on-patients-risk-assessment-during-covid-19-emergency/ 2024-02-29T14:11:03+00:00 https://www.meditrial.net/2020/03/romania-important-announcement-of-anmdmr-to-the-attention-of-companies-conducting-clinical-trials/ 2024-02-29T14:10:08+00:00 https://www.meditrial.net/2020/04/respirators-and-ventilators-supply-during-pandemic-guidance-for-us-versus-europe/ 2024-02-29T14:08:24+00:00 https://www.meditrial.net/2021/01/post-brexit-eu-relations-with-the-united-kingdom-and-impact-on-medical-devices/ 2024-02-29T14:05:00+00:00 https://www.meditrial.net/2020/03/portugal-ethics-committee-ceic-guidance-on-how-to-act-towards-covid-19-in-clinical-trials/ 2024-02-29T14:03:18+00:00 https://www.meditrial.net/2020/03/poland-authorities-suspend-inspection-of-clinical-trials-till-the-end-of-april-2020-due-to-covid-19/ 2024-02-29T14:01:20+00:00 https://www.meditrial.net/2020/05/one-million-have-recovered-but-fully-healed/ 2024-02-29T13:59:58+00:00 https://www.meditrial.net/2020/03/norway-noma-allows-changes-and-safety-measures-in-clinical-research-prior-to-approval-during-covid-19-emergency/ 2024-02-29T13:58:34+00:00 https://www.meditrial.net/2020/10/netherlands-notifications-of-clinical-investigations-with-medical-devices-to-ccmo-as-of-the-1st-of-october/ 2024-02-29T13:56:00+00:00 https://www.meditrial.net/2020/03/netherlands-central-research-committee-announces-approval-fastrack-for-trials-to-develop-covid-19-vaccines/ 2024-02-29T13:55:20+00:00 https://www.meditrial.net/2020/05/netherland-ccmo-announces-conditions-for-restarting-a-clinical-trials-in-clinical-research-units/ 2024-02-29T13:53:58+00:00 https://www.meditrial.net/2020/06/mpg-basic-course-for-investigators-deputies-and-members-of-the-clinical-study-group-new-at-the-meditrial-academy-berlin/ 2024-02-29T13:51:45+00:00 https://www.meditrial.net/2020/04/mhra-updates-specification-for-ventilators-to-be-used-in-uk-hospitals-during-covid-19-emergency/ 2024-02-29T13:50:15+00:00 https://www.meditrial.net/2020/05/mhra-regulatory-flexibilities-resulting-from-the-covid-19/ 2024-02-29T13:49:11+00:00 https://www.meditrial.net/2020/05/meditrial-swiss-office-reopens-after-covid-19-lock-down/ 2024-02-29T13:47:50+00:00 https://www.meditrial.net/2020/03/meditrial-provides-rapid-workflows-to-rescue-clinical-trials-during-pandemic/ 2024-02-29T13:46:29+00:00 https://www.meditrial.net/2020/03/nyc-squad/ 2024-02-29T13:43:37+00:00 https://www.meditrial.net/2020/05/meditrial-italian-team-is-back-at-work/ 2024-02-29T10:35:34+00:00 https://www.meditrial.net/2020/05/meditrial-italian-office-reopens-after-covid-19-lockdown/ 2024-02-29T10:32:34+00:00 https://www.meditrial.net/2020/03/meditrial-announces-free-helpline-to-support-clinical-research-during-covid-19-emergency/ 2024-02-29T10:24:48+00:00 https://www.meditrial.net/2020/06/meditrial-cmo-dr-monica-tocchi-joins-the-venturelab-expert-panel/ 2024-02-29T10:16:35+00:00 https://www.meditrial.net/2020/05/meditrial-berlin-office-reopens-after-covid-19-lockdown/ 2024-02-29T09:53:15+00:00 https://www.meditrial.net/2020/04/mdcg-publishes-new-guidances-on-equivalence-legacy-devices-pmcf-and-ventilators/ 2024-02-29T09:43:48+00:00 https://www.meditrial.net/2020/04/mdr-deferral-proposal-spot-the-difference/ 2024-02-26T17:00:11+00:00 https://www.meditrial.net/2020/03/proposal-to-postpone-mdr-for-one-year/ 2024-02-26T16:58:31+00:00 https://www.meditrial.net/2020/04/mdcg-possibility-to-postpone-or-undergo-remote-audit-for-medical-device-manufacturers-during-covid-19/ 2024-02-26T16:52:20+00:00 https://www.meditrial.net/2021/07/mdcg-outlines-rules-on-eudamed-registration-for-custom-made-and-legacy-devices/ 2024-02-26T16:46:14+00:00 https://www.meditrial.net/2020/05/mdcg-issues-guidance-on-safety-reporting-for-device-studies-under-mdr/ 2024-02-26T16:45:36+00:00 https://www.meditrial.net/2020/06/mdcg-issued-guidance-on-transitioning-devices-with-ancillary-substances-to-mdr/ 2024-02-26T16:44:18+00:00 https://www.meditrial.net/2020/03/lithuania-lithuanian-bioethics-committee-issues-guidelines-on-clinical-research-under-covid-19/ 2024-02-26T16:10:55+00:00 https://www.meditrial.net/2020/03/latvia-sam-recommendations-to-ensure-continuity-of-clinical-trials-during-pandemic/ 2024-02-26T16:07:57+00:00 https://www.meditrial.net/2020/03/italy-covid-19-infection-reaches-59-138-with-5-476-deaths-slowing-trends-of-new-cases-and-deaths-recorded-today-for-the-first-time/ 2024-02-26T15:59:57+00:00 https://www.meditrial.net/2020/03/italy-activates-procedures-safeguard-trials-during-pandemic/ 2024-02-26T12:32:21+00:00 https://www.meditrial.net/2020/05/isreael-monitoring-visits-in-hospitals-allowed-again/ 2024-02-26T12:26:55+00:00 https://www.meditrial.net/2020/03/israel-ministry-of-health-facilitates-clinical-trials-and-allows-study-products-delivery-to-patient-homes-during-the-coronavirus-outbreak/ 2024-02-26T12:22:48+00:00 https://www.meditrial.net/2020/03/ireland-hpra-provides-recommendations-for-clinical-research-management-under-covid-19/ 2024-02-26T12:16:42+00:00 https://www.meditrial.net/2020/04/international-regulators-pledge-collective-support-to-combat-covid-19-pandemic/ 2024-02-26T12:08:56+00:00 https://www.meditrial.net/2020/04/international-regulators-emphasize-the-need-for-reliable-evidence-on-covid-19-treatment/ 2024-02-26T11:53:42+00:00 https://www.meditrial.net/2020/04/imdrf-issues-guidances-on-cybersecurity-personalized-devices-conformity-assessment-bodies-and-terminologies-for-categorized-adverse-event-reporting-aer/ 2024-02-26T11:42:11+00:00 https://www.meditrial.net/2020/03/hungary-exceptional-measures-for-clinical-studies-under-covid-19/ 2024-02-26T11:39:00+00:00 https://www.meditrial.net/2020/03/greece-aeo-changes-opening-hours-during-covid-19-emergency/ 2024-02-26T11:19:29+00:00 https://www.meditrial.net/2020/05/germany-dimdi-merges-into-bfarm/ 2024-02-26T11:15:21+00:00 https://www.meditrial.net/2020/03/germany-bfarm-recommendations-for-clinical-trials-with-medical-devices-during-the-covid-19-pandemic/ 2024-02-26T11:12:52+00:00 https://www.meditrial.net/2020/03/germany-bfarm-provides-support-for-ongoing-clinical-trials/ 2024-02-26T11:10:55+00:00 https://www.meditrial.net/2020/05/germany-bfarm-and-pei-issued-supplementary-recommendations-on-management-of-clinical-trials-during-covid-19-pandemic/ 2024-02-26T11:08:52+00:00 https://www.meditrial.net/2020/05/free-webinar-covid-19-and-mental-health-phase-3-get-ready-to-win-in-the-new-normality/ 2024-02-26T11:05:15+00:00 https://www.meditrial.net/2020/03/france-ansm-offers-practical-solution-to-manage-clinical-trials-amid-the-crisis/ 2024-02-26T11:01:22+00:00 https://www.meditrial.net/2020/03/finland-fimea-requires-on-site-monitoring-reduction-during-covid-19-emergency/ 2024-02-26T10:58:42+00:00 https://www.meditrial.net/2020/04/fda-update-for-medical-device-manufacturers-in-cares-act/ 2024-02-26T10:57:19+00:00 https://www.meditrial.net/2020/06/fda-mystudies-app-offers-platform-for-electronic-informed-consent/ 2024-02-26T10:55:19+00:00 https://www.meditrial.net/2020/05/fda-updates-on-surveillance-inspections-during-covid-19/ 2024-02-26T09:44:34+00:00 https://www.meditrial.net/2020/05/fda-updates-guidance-on-conduct-of-clinical-trials-during-covid-19/ 2024-02-26T09:43:11+00:00 https://www.meditrial.net/2020/05/fda-released-recommendations-for-sponsors-requesting-euas-for-decontamination-and-bioburden-reduction-systems-for-surgical-masks-and-respirators-during-the-covid-19-emergency/ 2024-02-26T09:34:50+00:00 https://www.meditrial.net/2020/06/fda-provides-statistical-guidance-for-trials-during-covid-19/ 2024-02-26T09:26:25+00:00 https://www.meditrial.net/2020/05/fda-issues-guidance-on-premarket-approval-pma-and-humanitarian-device-exemption-hde-supplements-during-covid-19/ 2024-02-26T09:10:23+00:00 https://www.meditrial.net/2020/04/fda-issued-a-guidance-on-remote-digital-pathology-and-non-invasive-fetal-and-maternal-monitoring-devices/ 2024-02-23T16:59:16+00:00 https://www.meditrial.net/2020/08/eu-medical-device-single-audit-program-guidance-by-the-eu-commissions-medical-device-coordination-group/ 2024-02-23T16:35:16+00:00 https://www.meditrial.net/2020/05/fda-issued-a-guidance-on-conduct-of-clinical-trials-of-medical-products-during-covid-19/ 2024-02-07T16:16:06+00:00 https://www.meditrial.net/2020/03/meditrial-rapid-workflows-to-rescue-clinical-trials-during-covid-emergency-as-recommended-by-us-fda/ 2024-02-07T16:14:45+00:00 https://www.meditrial.net/2020/05/fda-cdrh-issues-guidance-on-notifications-of-medical-device-shortages-during-covid-19/ 2024-02-07T16:13:06+00:00 https://www.meditrial.net/2020/04/fda-announces-activities-against-covid-19-in-a-new-at-a-glance-summary/ 2024-02-07T16:10:56+00:00 https://www.meditrial.net/2020/04/fda-and-cdc-fact-sheet-on-use-of-cloth-face-coverings-against-covid-19/ 2024-02-07T16:09:22+00:00 https://www.meditrial.net/2020/04/european-council-modifies-the-ec-proposal-for-mdr-delay/ 2024-02-07T16:07:23+00:00 https://www.meditrial.net/2020/03/european-commission-ema-and-hta-issue-harmonized-guidance-for-clinical-trials-during-the-covid-19-pandemic/ 2024-02-07T15:54:29+00:00 https://www.meditrial.net/2020/04/european-commission-welcomes-the-mdr-delay-adoption-by-the-european-parliament-and-the-council/ 2024-02-07T15:52:28+00:00 https://www.meditrial.net/2020/06/european-commission-updates-on-mdr-and-ivdr-implementation-timeline/ 2024-02-07T15:50:33+00:00 https://www.meditrial.net/2020/07/eu-availability-and-capacity-of-notified-bodies-to-carry-out-conformity-assessments-for-covid-19-related-medical-devices-and-in-vitro-diagnostic-medical-devices/ 2024-02-02T12:24:26+00:00 https://www.meditrial.net/2020/04/eu-members-states-and-european-commission-introduce-mobile-apps-to-gradually-loosen-confinement/ 2024-02-02T12:16:25+00:00 https://www.meditrial.net/2020/07/eu-agencies-commends-sponsors-to-ensure-post-brexit-compliance-with-clinical-trial-rules/ 2024-02-02T11:58:44+00:00 https://www.meditrial.net/2020/03/estonia-regulatory-clarification-for-all-concerned-parties-in-clinical-trials/ 2024-02-02T11:56:18+00:00 https://www.meditrial.net/2020/07/ema-points-to-consider-on-implications-of-covid-19-on-methodological-aspects-of-ongoing-clinical-trials/ 2024-02-02T11:53:30+00:00 https://www.meditrial.net/2020/05/ema-global-regulators-work-towards-alignment-on-policy-approaches-and-regulatory-flexibility-during-covid-19/ 2024-02-02T11:50:42+00:00 https://www.meditrial.net/2020/05/ema-updates-its-governance-during-covid-19-pandemic/ 2024-02-02T11:48:58+00:00 https://www.meditrial.net/2020/04/ema-updated-the-guidance-on-the-management-of-clinical-trials-during-covid-19-pandemic/ 2024-02-02T11:41:53+00:00 https://www.meditrial.net/2020/03/ema-implications-of-coronavirus-disease-covid-19-on-methodological-aspects-of-ongoing-clinical-trials/ 2024-02-02T11:39:10+00:00 https://www.meditrial.net/2020/04/ema-guidance-on-the-management-of-clinical-trials-during-the-covid-19-pandemic/ 2024-02-02T11:24:14+00:00 https://www.meditrial.net/2020/05/ema-calls-for-high-quality-observational-research-in-context-of-covid-19/ 2024-02-02T10:53:33+00:00 https://www.meditrial.net/2021/09/electronic-submission-template-for-medical-device-510k-submissions/ 2024-02-02T10:49:34+00:00 https://www.meditrial.net/2020/07/meditrial-present-dr-tocchi-lecture-for-weill-cornell-medicine/ 2024-02-02T10:42:51+00:00 https://www.meditrial.net/2020/03/denmark-extraordinary-measures-for-clinical-trials-due-to-covid-19/ 2024-02-02T10:35:12+00:00 https://www.meditrial.net/2020/06/czech-republic-opinion-of-the-sukl-department-of-clinical-trials-on-ongoing-clinical-trials-and-on-clinical-trials-not-yet-initiated-in-relation-to-covid-19/ 2024-02-02T10:24:34+00:00 https://www.meditrial.net/2020/03/czech-republic-authority-sukl-issues-clinical-trial-instructions-for-subject-safety-and-data-validity-during-covid-19-emergency/ 2024-02-02T10:16:28+00:00 https://www.meditrial.net/2020/06/covid-19-the-challenge-of-the-italian-industry-during-the-conversion-the-production-how-to-start-again-and-succeed/ 2024-02-01T16:59:23+00:00 https://www.meditrial.net/2020/04/imperial-college-london-covid-19-webinar-april-2/ 2024-02-01T16:57:35+00:00 https://www.meditrial.net/2020/03/columbia-updates-on-clinical-trials-submission-during-covid-19/ 2024-02-01T16:54:53+00:00 https://www.meditrial.net/2020/04/columbia-procedures-not-related-to-the-covid-19-emergency/ 2024-02-01T16:43:42+00:00 https://www.meditrial.net/2020/09/canada-health-canada-releases-guidance-on-the-conduct-of-clinical-trials-during-covid-19-pandemic/ 2024-02-01T16:41:27+00:00 https://www.meditrial.net/2020/03/belgium-famhp-recommends-electronic-submission-during-covid-19-emergency/ 2024-02-01T16:16:31+00:00 https://www.meditrial.net/2020/05/austria-basg-issues-information-on-the-withdrawal-of-measures-for-clinical-trials-at-the-end-of-the-pandemic/ 2024-02-01T15:08:04+00:00 https://www.meditrial.net/2020/03/austria-basg-on-safety-measures-for-clinical-research-during-covid-19-emergency/ 2024-02-01T15:07:37+00:00 https://www.meditrial.net/2020/05/win-kols-and-work-with-partners-virtual-training-by-dr-monica-tocchi-for-venturelab/ 2024-02-01T14:12:57+00:00 https://www.meditrial.net/2021/01/iso-issues-standard-revision-iso10993-232021-biological-evaluation-of-medical-devices-part-23-tests-for-irritation/ 2023-04-21T11:02:51+00:00 https://www.meditrial.net/2021/01/us-cdrh-plans-full-launch-of-asca-pilot-program-in-2021/ 2023-04-21T10:48:30+00:00 https://www.meditrial.net/2021/03/eu-eudamed-udi-device-registration-and-certificates-and-notified-bodies-modules-available-by-september-2021/ 2023-04-21T09:20:12+00:00 https://www.meditrial.net/2021/03/eu-mdcg-issues-qa-on-custom-made-devices/ 2023-04-21T09:14:17+00:00 https://www.meditrial.net/2020/12/uk-get-ready-for-uk-market-access-and-the-new-ukca-requirements/ 2023-03-31T16:32:08+00:00 https://www.meditrial.net/2020/11/eu-mdcg-releases-ivd-classification-guidance/ 2023-03-31T16:17:03+00:00 https://www.meditrial.net/2021/03/eu-european-union-and-commission-launch-eu4health-funding-program-to-boost-healthcare-digitalization-and-make-devices-more-accessible/ 2023-03-31T13:23:04+00:00 https://www.meditrial.net/2021/03/eu-mdcg-issues-guidance-on-harmonised-administrative-practices-and-alternative-technical-solutions-until-eudamed-is-fully-functional/ 2023-03-31T13:15:38+00:00 https://www.meditrial.net/2021/02/eu-the-european-commission-issues-a-guidance-on-management-of-legacy-devices-in-eudamed/ 2023-03-31T13:14:00+00:00 https://www.meditrial.net/2021/02/eu-ema-expands-the-use-of-remote-source-data-verification-in-clinical-trials/ 2023-03-31T13:12:41+00:00 https://www.meditrial.net/2021/03/international-council-for-harmonisation-ich-to-issue-revision-of-e6-r2-good-clinical-practice-in-fall-2021/ 2023-03-31T12:43:00+00:00 https://www.meditrial.net/2021/04/eu-commission-drives-digital-health-by-establishing-new-european-health-and-digital-executive-agency/ 2023-03-31T11:05:13+00:00 https://www.meditrial.net/2021/04/eu-the-mdcg-informs-on-how-to-handle-class-d-ivds-during-transition-to-new-regulation-ivdr/ 2023-03-31T09:46:24+00:00 https://www.meditrial.net/2021/04/eu-mdcg-issued-a-guidance-on-standardization-for-medical-devices/ 2023-03-31T09:37:46+00:00 https://www.meditrial.net/2021/04/austria-medical-device-and-ivd-clinical-trials-submission-process-changes-during-transition-to-mdr/ 2023-03-31T09:12:27+00:00 https://www.meditrial.net/2021/05/meditrial-mdr-diversity-germany-clinical-trials/ 2023-03-31T09:04:26+00:00 https://www.meditrial.net/2021/07/mhra-announces-combined-review-of-clinical-trials-for-medicinal-products/ 2023-03-29T15:54:25+00:00 https://www.meditrial.net/2021/07/france-ansm-updates-guidelines-and-forms-for-a-scientific-opinion-for-a-medical-device-incorporating-a-medicinal-substance/ 2023-03-29T15:54:00+00:00 https://www.meditrial.net/2021/09/fda-ema-parallel-scientific-advice-pilot-program-for-complex-generic-hybrid-products/ 2023-03-29T15:53:12+00:00 https://www.meditrial.net/2021/10/prefer-patient-input-to-decision-making-under-evaluation/ 2023-03-29T15:51:23+00:00 https://www.meditrial.net/2021/11/content-of-premarket-submission-for-device-software-functions/ 2023-03-29T15:49:17+00:00 https://www.meditrial.net/2021/12/mdcg-2021-28-substantial-modification-of-clinical-investigation-under-medical-device-regulation/ 2023-03-29T15:49:01+00:00 https://www.meditrial.net/2022/01/eudamed-actor-module-faqs-update/ 2023-03-29T15:48:06+00:00 https://www.meditrial.net/2022/01/guideline-for-the-notification-of-serious-breaches-of-regulation-eu-no-536-2014-or-the-clinical-trial-protocol/ 2023-03-29T14:47:59+00:00 https://www.meditrial.net/2022/01/mdcg-2022-1-notice-to-third-country-manufacturers-of-sars-cov-2-in-vitro-diagnostic-medical-devices/ 2023-03-29T14:47:07+00:00 https://www.meditrial.net/2022/01/mdcg-2022-2-guidance-on-general-principles-of-clinical-evidence-for-in-vitro-diagnostic-medical-devices-ivds/ 2023-03-29T14:46:55+00:00 https://www.meditrial.net/2022/02/new-fda-guidance-good-anda-submission-practices/ 2023-03-29T14:26:12+00:00 https://www.meditrial.net/2022/02/pic-s-revises-gmp-guide-to-reflect-new-eu-clinical-trials-regulation/ 2023-03-29T14:25:58+00:00 https://www.meditrial.net/2022/02/the-mdcg-updates-the-ivdr-implementation-and-preparation-plan-eu-2017-746/ 2023-03-29T14:15:44+00:00 https://www.meditrial.net/2022/02/us-the-fda-has-finalized-guidance-on-the-use-of-premarket-pathways-for-combination-products/ 2023-03-29T14:06:37+00:00 https://www.meditrial.net/2022/02/new-guidance-mdcg-2022-3-verification-of-manufactured-class-d-ivds-by-notified-bodies/ 2023-03-29T14:06:17+00:00 https://www.meditrial.net/2022/02/new-mdcg-guidance-2022-4/ 2023-03-29T14:05:32+00:00 https://www.meditrial.net/2022/03/handover-of-expert-panels-on-medical-devices-and-in-vitro-diagnostics-to-ema/ 2023-03-29T14:04:04+00:00 https://www.meditrial.net/2022/03/spanish-data-protection-authority-approves-the-first-industry-code-of-conduct-to-enable-compliance-of-clinical-research-and-pharmacovigilance-with-the-gdpr/ 2023-03-29T14:02:09+00:00 https://www.meditrial.net/2022/03/bvmed-and-snitem-overcoming-the-mdr-implementation-bottleneck/ 2023-03-29T14:01:53+00:00 https://www.meditrial.net/2022/04/ema-has-published-an-updated-version-of-its-good-clinical-practice-qa/ 2023-03-29T14:01:51+00:00 https://www.meditrial.net/2022/04/ema-advice-for-ukraine-clinical-trials/ 2023-03-29T14:01:43+00:00 https://www.meditrial.net/2022/04/eudamed-udi-devices-updated-technical-documentation-module/ 2023-03-29T14:01:39+00:00 https://www.meditrial.net/2022/04/prac-strategy-on-pharmacovigilance/ 2023-03-29T13:55:52+00:00 https://www.meditrial.net/2022/09/the-contribution-of-patient-associations-in-clinical-trials/ 2022-10-05T11:20:42+00:00 https://www.meditrial.net/2022/09/il-contributo-delle-associazioni-pazienti-negli-studi-clinici/ 2022-09-28T16:04:24+00:00 https://www.meditrial.net/2022/09/limportanza-del-data-monitoring-committee-nei-trial-di-oggi-e-domani/ 2022-09-28T11:03:04+00:00 https://www.meditrial.net/2022/09/the-importance-of-the-data-monitoring-committee-in-the-trials-of-today-and-tomorrow/ 2022-09-28T11:02:03+00:00 https://www.meditrial.net/2022/09/early-feasibility-studies-on-devices-doing-it-sooner-to-avoid-trial-failure/ 2022-09-28T10:21:58+00:00 https://www.meditrial.net/2022/09/studi-di-fattibilita-precoce-sui-devices-fare-prima-per-evitare-il-fallimento-dei-trial/ 2022-09-28T10:10:51+00:00 https://www.meditrial.net/2022/09/samd-intelligenza-artificiale-e-machine-learning-i-primi-passi-degli-enti-regolatori/ 2022-09-16T19:54:37+00:00 https://www.meditrial.net/2022/08/studi-clinici-cosi-i-biomarker-aiutano-la-ricerca/ 2022-09-16T19:54:06+00:00 https://www.meditrial.net/2022/09/samd-artificial-intelligence-and-machine-learning-regulators-first-steps/ 2022-09-16T16:01:49+00:00 https://www.meditrial.net/2022/09/clinical-trials-how-biomarkers-help-research/ 2022-09-16T15:54:02+00:00 https://www.meditrial.net/2022/06/the-new-good-clinical-practices-for-in-vitro-diagnostic-devices/ 2022-08-04T14:21:10+00:00 https://www.meditrial.net/2022/06/le-nuove-good-clinical-practice-per-i-dispositivi-diagnostici-in-vitro/ 2022-08-04T14:11:33+00:00 https://www.meditrial.net/2022/07/disegno-degli-studi-clinici-la-rivoluzione-deinuovi-principi-statistici/ 2022-08-04T14:07:45+00:00