Rezultati pretraživanja
  1. 31. sij

    Down in London today - Order of the day: Lean Compliance

  2. prije 17 sati

    The EU Medical Device Regulation: What’s Next?

  3. prije 3 sata

    Time is running out to complete our survey on MDR and compliance. Complete it before 9 Feb for a chance to win a 2-day MedTech Summit pass

  4. prije 2 sata

    Turussa oli kevät, kun virkamies vieraili Tyks:ssa keskustelemassa laitetutkimuksista.

  5. 4. velj

    Brexit information for Medical Devices:

    1 proslijeđeni tweet
  6. 3. velj

    Calling all and ! We are working in conjunction with the team at to deliver efficient advisory and support services to help you ensure compliance with your obligations under & . Don't hesitate to call us.

    We are helping , & ensure they are compliant with their obligations under and . If you need any advice or support in your organisation, please reach out to us at mdr@thecompliance.team and we will be happy to help.
  7. 3. velj

    We are helping , & ensure they are compliant with their obligations under and . If you need any advice or support in your organisation, please reach out to us at mdr@thecompliance.team and we will be happy to help.

    1 korisnik označava da mu se sviđa
  8. 3. velj

    Today we're with our member company Thermo Fisher to discuss IVDs, the , and .

  9. 3. velj

    Know execs’ top 10 questions about Europe’s . Register today for the free Feb. 10 webinar presented by ’s Sue Spencer.

    2 korisnika označavaju da im se sviđa
  10. 3. velj

    SFL’s CEO is presenting on “Regulating tomorrow's : promoting and while maintaining consumer and ” at the Swiss HLG2020 Conference.

  11. 3. velj

    ¿Sabía que la nueva Regulación de en el Mercado para e se aplica además de las y ? Este articulo en el Journal of Medical Device Regulation analiza el impacto para la industria de dispositivos médicos.

  12. 3. velj

    Wussten Sie, dass die neue zusätzlich zu und gilt? Jetzt in der Februar-Ausgabe des Journal of Medical Device Regulation: Analyse der Auswirkungen der Marktüberwachungsverordnung auf die -Branche.

  13. 1. velj

    Preparation for MDR and is ramping up, but how close to compliance is the device industry? We are asking insiders in one of the biggest surveys of its kind. Complete it here for a chance to win a 2-day MedTech Summit pass

  14. 31. sij

    is an integral part of technical documentation. As it demonstrates the complete picture of , author it as per the standards. For assistance, consult

    1 proslijeđeni tweet 3 korisnika označavaju da im se sviđa
  15. 31. sij

    Get up to speed on the EU’s . Register for the free Feb. 10 webinar presented by ’s Sue Spencer.

  16. 30. sij

    The European Commission has provided updated information on the and designation status of Notified Bodies. Read more-->

    1 proslijeđeni tweet 2 korisnika označavaju da im se sviđa
  17. 30. sij

    Myös ohjelmistot voivat aiheuttaa vakavaa haittaa potilaille. Siksi mm. huolellinen riskianalyysi ja kattava kliininen arviointi ovat välttämättömiä. Potilas kuoli, kun uuden Apotti-järjestelmän sekavuus haittasi hoitoa.

    2 korisnika označavaju da im se sviđa
  18. 29. sij

    have a new podcast - . First up? Director, Oliver Bisazza, explains upcoming changes to the CE marking for . And how and raise the game.

    1 proslijeđeni tweet 1 korisnik označava da mu se sviđa
  19. 29. sij

    This February, any device manufacturers needing help preparing for the new and can attend Medical Design & Manufacturing West's 2020 paid conference in Anaheim, CA. Click below for more information.

  20. 29. sij

    Join NAMSA on Feb. 19 for our latest webinar to gain a better understanding of IVDR QMS requirements, ISO 14971 and other critical components to achieve IVDR conformity.

    1 proslijeđeni tweet 2 korisnika označavaju da im se sviđa

Nema rezultata.

Čini se da učitavanje traje već neko vrijeme.

Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.