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Medical Device News April 2024 Regulatory Update
MP3•Maison d'episode
Manage episode 410535770 series 2591977
Contenu fourni par Monir El Azzouzi. Tout le contenu du podcast, y compris les épisodes, les graphiques et les descriptions de podcast, est téléchargé et fourni directement par Monir El Azzouzi ou son partenaire de plateforme de podcast. Si vous pensez que quelqu'un utilise votre œuvre protégée sans votre autorisation, vous pouvez suivre le processus décrit ici https://fr.player.fm/legal.
Sponsor:
Medboard: https://www.medboard.com/
EU
- MDR and IVDR national languages update – France accepts English
- Which devices for Expert Panel – Active Implantable Device on Top: https://health.ec.europa.eu/document/download/4c43abea-b989-434b-9ac1-94134bf1a538_en?filename=md_annual-overview-cecp-2022-2023_en.pdf
- 94.4% for Class III implantable and 5.6% for Class Iib Administer or remove medicinal products
- On Class III implantable – Top is with Active Implantable Devices
- Exempt devices are mainly within 3 categories (Main reason: Modification of a device already marketed):
- Vascular and cardiac prostheses
- Orthopaedic prostheses, osteosynthesis devices, devices for tendon and ligaments synthesis
- Implantable prosthetic and osteosynthesis devices
- Annex XVI: Is Brain Stimulation device risk? – SCHEER should evaluate by End 2025: https://health.ec.europa.eu/document/download/e6de1e88-2821-48f6-98f9-a56ea61cbfad_en?filename=scheer_q_031.pdf
- SCHEER = Scientific Committee on Health, Environmental and Emerging Risks
- SCHEER on Phtalate – Update of the guidelines: https://health.ec.europa.eu/consultations/scheer-public-consultation-preliminary-update-scheer-guidelines-benefit-risk-assessment-presence_en
- Consultation until April 28th, 2024
- MDCG subgroup Agenda – What is coming?: https://health.ec.europa.eu/document/download/f588a5c8-57af-48aa-808f-1d9c02f4925a_en?filename=mdcg_ongoing-guidance_0.pdf
- MDCG 2024-3 on CIP – Clinical Investigation: https://health.ec.europa.eu/document/download/690de85a-ac17-45ea-bb32-7839540c25c4_en?filename=mdcg_2024-3_en.pdf
- New Notified Body RISE Sweden – Welcome to the team 3033: https://api.tech.ec.europa.eu/nando-prod/files?repo=nando&id=d37c034bc695d2e143b5145b4cb7cd73caf8983c&group=NOTIFICATION&download=true
- 44 MDR NB
- 12 IVDR NB
UK
- MHRA: Electrical Devices in Clinical Trials – Advice on application with separate document: https://assets.publishing.service.gov.uk/media/65fb0d66aa9b76001dfbdc28/MHRA_Electrical_Guidance_for_Clinical_Investigations_Modified_12_Feb.pdf
Ireland
- HPRA Newsletter- IVD, Eudamed, Custom-made, Clinical trials: https://www.hpra.ie/docs/default-source/publications-forms/newsletters/hpra-medical-devices-newsletter-issue-57-february-2024.pdf
Turkey
- Reminder on MDR transition period – May 26th, 2024: https://titck.gov.tr/storage/Archive/2024/announcement/duyurumetni_67231ed0-2553-4708-8231-7951c767e066.pdf
- Turkey strongly inform the different parties regarding MDR transition
Events
- RAPS Euro Convergence – May 6-8 in Berlin-Germany: https://www.raps.org/europe-2024/home
- Medtech Conf Map: https://medtechconf.com/event/connect-with-european-andinternational-regulatoryaffairs-peers-in-berlin-2/
Services
- Packaging for Medical and Pharmaceutical – Design, Manufacturing and delivery: https://easymedicaldevice.com/packaging-for-medical-devices/
ROW
USA
- Ban devices – Electrical Stimulation Devices for Self-injurious or Aggressive Behavior: https://www.fda.gov/medical-devices/medical-device-safety/medical-device-bans
- CNN article: https://edition.cnn.com/2024/03/25/health/fda-ban-electrical-stimulation-devices/index.html
- Comments open until May 28, 2024: https://www.fda.gov/medical-devices/medical-devices-news-and-events/fda-proposes-new-ban-electrical-stimulation-devices-self-injurious-or-aggressive-behavior
- Bans
- Prosthetic Hair Fibers since 1983
- Powdered Surgeon’s Gloves since 2017
- Electrical Stimulation Devices for Self-injurious or Aggressive Behavior since March 2024
- Animal Studie for Dental Bone Grafting devices – Choose the right animal Model: https://www.fda.gov/media/177340/download
- Minimum of 3 animals
- Animal Model: Canine and Porcine model instead of rodents
- FDA: Deviations on Neuralink lab – Animal Study good practices: https://www.reuters.com/business/healthcare-pharmaceuticals/fda-finds-problems-animal-lab-run-by-musks-brain-implant-company-2024-02-29/
- Calibration of equipment’s are not done
- Quality officials not signing documents
Australia
- Vigilance Reporting in Australia – For Recall and non-Recall: https://www.tga.gov.au/sites/default/files/2024-03/uniform-recall-procedure-therapeutic-goods-urptg.pdf
- Recall action Template: https://www.tga.gov.au/resources/resource/forms/recall-action-templates
Saudi Arabia
- Guidance on Surgical Sutures – This contains some cheat code: https://www.sfda.gov.sa/sites/default/files/2024-03/%28MDS-G021%29En.pdf
- Endpoints that should be addressed
- Laboratories should be ISO/IEC 17025
- Shelf life should follow ASTM F1980
Brazil
- MOU between Brazil and Paraguay – Memorandum of Understanding: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-e-agencia-reguladora-do-paraguai-assinam-primeiro-memorando-de-entendimento
- Bilateral cooperation on health surveillance
- Strenghtening regulatory capacity
- GMP validity from two to four years – If certified through MDSAP: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-amplia-para-quatro-anos-prazo-de-validade-do-certificado-de-boas-praticas-de-fabricacao
- Prioritize registration of Dengue Diagnosis Devices – Submit Now: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-prioriza-registro-de-dispositivos-para-diagnostico-da-dengue
- Combat dengue epidemic as a matter of urgency
India
- CDSCO: PSUR through online portal – From April 1st, 2024: https://cdsco.gov.in/opencms/opencms/system/modules/CDSCO.WEB/elements/download_file_division.jsp?num_id=MTEwMTI=
- Online portal: https://www.cdscomdonline.gov.in/NewMedDev/Homepage
Malaysia
- Malaysia Faster approval – Establishment license application: https://www.mda.gov.my/index.php/announcement/1377-faster-approval-for-establishment-license-application-complete-applications-processed-within-14-21-working-days
- 14 to 21 Working days from date of application
- List of documents within the link
China
- China Guidelines on registration – Specific products: https://www.cmde.org.cn/xwdt/zxyw/20240318133300123.html
- Corneal Topograph
- Laparoscopic surgery system
- Optical Radiation Safety device
- Monkeypox virus nucleid acid detections agent: https://www.cmde.org.cn/xwdt/zxyw/20240318111545184.html
Podcast
- Podcast Nostalgia
- Episode 275 – FDA aligns QMSR with ISO 13485 (Naveen Agarwal): https://podcast.easymedicaldevice.com/275-2/
- Episode 276 – How to do Postmarketing Surveillance to right way? (Steve Curran): https://podcast.easymedicaldevice.com/276-2/
- Episode 277 – How to benefit from Survey to build Clinical Evidence? (Cesare Magri): https://podcast.easymedicaldevice.com/277-2/
Easy Medical Device
- info@easymedicaldevice.com
Social Media to follow
- Monir El Azzouzi Linkedin: https://linkedin.com/in/melazzouzi
- Twitter: https://twitter.com/elazzouzim
- Pinterest: https://www.pinterest.com/easymedicaldevice
- Instagram: https://www.instagram.com/easymedicaldevice
The post Medical Device News April 2024 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
292 episodes
MP3•Maison d'episode
Manage episode 410535770 series 2591977
Contenu fourni par Monir El Azzouzi. Tout le contenu du podcast, y compris les épisodes, les graphiques et les descriptions de podcast, est téléchargé et fourni directement par Monir El Azzouzi ou son partenaire de plateforme de podcast. Si vous pensez que quelqu'un utilise votre œuvre protégée sans votre autorisation, vous pouvez suivre le processus décrit ici https://fr.player.fm/legal.
Sponsor:
Medboard: https://www.medboard.com/
EU
- MDR and IVDR national languages update – France accepts English
- Which devices for Expert Panel – Active Implantable Device on Top: https://health.ec.europa.eu/document/download/4c43abea-b989-434b-9ac1-94134bf1a538_en?filename=md_annual-overview-cecp-2022-2023_en.pdf
- 94.4% for Class III implantable and 5.6% for Class Iib Administer or remove medicinal products
- On Class III implantable – Top is with Active Implantable Devices
- Exempt devices are mainly within 3 categories (Main reason: Modification of a device already marketed):
- Vascular and cardiac prostheses
- Orthopaedic prostheses, osteosynthesis devices, devices for tendon and ligaments synthesis
- Implantable prosthetic and osteosynthesis devices
- Annex XVI: Is Brain Stimulation device risk? – SCHEER should evaluate by End 2025: https://health.ec.europa.eu/document/download/e6de1e88-2821-48f6-98f9-a56ea61cbfad_en?filename=scheer_q_031.pdf
- SCHEER = Scientific Committee on Health, Environmental and Emerging Risks
- SCHEER on Phtalate – Update of the guidelines: https://health.ec.europa.eu/consultations/scheer-public-consultation-preliminary-update-scheer-guidelines-benefit-risk-assessment-presence_en
- Consultation until April 28th, 2024
- MDCG subgroup Agenda – What is coming?: https://health.ec.europa.eu/document/download/f588a5c8-57af-48aa-808f-1d9c02f4925a_en?filename=mdcg_ongoing-guidance_0.pdf
- MDCG 2024-3 on CIP – Clinical Investigation: https://health.ec.europa.eu/document/download/690de85a-ac17-45ea-bb32-7839540c25c4_en?filename=mdcg_2024-3_en.pdf
- New Notified Body RISE Sweden – Welcome to the team 3033: https://api.tech.ec.europa.eu/nando-prod/files?repo=nando&id=d37c034bc695d2e143b5145b4cb7cd73caf8983c&group=NOTIFICATION&download=true
- 44 MDR NB
- 12 IVDR NB
UK
- MHRA: Electrical Devices in Clinical Trials – Advice on application with separate document: https://assets.publishing.service.gov.uk/media/65fb0d66aa9b76001dfbdc28/MHRA_Electrical_Guidance_for_Clinical_Investigations_Modified_12_Feb.pdf
Ireland
- HPRA Newsletter- IVD, Eudamed, Custom-made, Clinical trials: https://www.hpra.ie/docs/default-source/publications-forms/newsletters/hpra-medical-devices-newsletter-issue-57-february-2024.pdf
Turkey
- Reminder on MDR transition period – May 26th, 2024: https://titck.gov.tr/storage/Archive/2024/announcement/duyurumetni_67231ed0-2553-4708-8231-7951c767e066.pdf
- Turkey strongly inform the different parties regarding MDR transition
Events
- RAPS Euro Convergence – May 6-8 in Berlin-Germany: https://www.raps.org/europe-2024/home
- Medtech Conf Map: https://medtechconf.com/event/connect-with-european-andinternational-regulatoryaffairs-peers-in-berlin-2/
Services
- Packaging for Medical and Pharmaceutical – Design, Manufacturing and delivery: https://easymedicaldevice.com/packaging-for-medical-devices/
ROW
USA
- Ban devices – Electrical Stimulation Devices for Self-injurious or Aggressive Behavior: https://www.fda.gov/medical-devices/medical-device-safety/medical-device-bans
- CNN article: https://edition.cnn.com/2024/03/25/health/fda-ban-electrical-stimulation-devices/index.html
- Comments open until May 28, 2024: https://www.fda.gov/medical-devices/medical-devices-news-and-events/fda-proposes-new-ban-electrical-stimulation-devices-self-injurious-or-aggressive-behavior
- Bans
- Prosthetic Hair Fibers since 1983
- Powdered Surgeon’s Gloves since 2017
- Electrical Stimulation Devices for Self-injurious or Aggressive Behavior since March 2024
- Animal Studie for Dental Bone Grafting devices – Choose the right animal Model: https://www.fda.gov/media/177340/download
- Minimum of 3 animals
- Animal Model: Canine and Porcine model instead of rodents
- FDA: Deviations on Neuralink lab – Animal Study good practices: https://www.reuters.com/business/healthcare-pharmaceuticals/fda-finds-problems-animal-lab-run-by-musks-brain-implant-company-2024-02-29/
- Calibration of equipment’s are not done
- Quality officials not signing documents
Australia
- Vigilance Reporting in Australia – For Recall and non-Recall: https://www.tga.gov.au/sites/default/files/2024-03/uniform-recall-procedure-therapeutic-goods-urptg.pdf
- Recall action Template: https://www.tga.gov.au/resources/resource/forms/recall-action-templates
Saudi Arabia
- Guidance on Surgical Sutures – This contains some cheat code: https://www.sfda.gov.sa/sites/default/files/2024-03/%28MDS-G021%29En.pdf
- Endpoints that should be addressed
- Laboratories should be ISO/IEC 17025
- Shelf life should follow ASTM F1980
Brazil
- MOU between Brazil and Paraguay – Memorandum of Understanding: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-e-agencia-reguladora-do-paraguai-assinam-primeiro-memorando-de-entendimento
- Bilateral cooperation on health surveillance
- Strenghtening regulatory capacity
- GMP validity from two to four years – If certified through MDSAP: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-amplia-para-quatro-anos-prazo-de-validade-do-certificado-de-boas-praticas-de-fabricacao
- Prioritize registration of Dengue Diagnosis Devices – Submit Now: https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2024/anvisa-prioriza-registro-de-dispositivos-para-diagnostico-da-dengue
- Combat dengue epidemic as a matter of urgency
India
- CDSCO: PSUR through online portal – From April 1st, 2024: https://cdsco.gov.in/opencms/opencms/system/modules/CDSCO.WEB/elements/download_file_division.jsp?num_id=MTEwMTI=
- Online portal: https://www.cdscomdonline.gov.in/NewMedDev/Homepage
Malaysia
- Malaysia Faster approval – Establishment license application: https://www.mda.gov.my/index.php/announcement/1377-faster-approval-for-establishment-license-application-complete-applications-processed-within-14-21-working-days
- 14 to 21 Working days from date of application
- List of documents within the link
China
- China Guidelines on registration – Specific products: https://www.cmde.org.cn/xwdt/zxyw/20240318133300123.html
- Corneal Topograph
- Laparoscopic surgery system
- Optical Radiation Safety device
- Monkeypox virus nucleid acid detections agent: https://www.cmde.org.cn/xwdt/zxyw/20240318111545184.html
Podcast
- Podcast Nostalgia
- Episode 275 – FDA aligns QMSR with ISO 13485 (Naveen Agarwal): https://podcast.easymedicaldevice.com/275-2/
- Episode 276 – How to do Postmarketing Surveillance to right way? (Steve Curran): https://podcast.easymedicaldevice.com/276-2/
- Episode 277 – How to benefit from Survey to build Clinical Evidence? (Cesare Magri): https://podcast.easymedicaldevice.com/277-2/
Easy Medical Device
- info@easymedicaldevice.com
Social Media to follow
- Monir El Azzouzi Linkedin: https://linkedin.com/in/melazzouzi
- Twitter: https://twitter.com/elazzouzim
- Pinterest: https://www.pinterest.com/easymedicaldevice
- Instagram: https://www.instagram.com/easymedicaldevice
The post Medical Device News April 2024 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir
292 episodes
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