• 09.10.2019

  Jurisdictional Update from Australia, 17.09.2019 (Tracey Duffy, Medical Devices and Product Quality Division Department of Health, Australia)

• 09.10.2019

  Regulatory and Policy Updates. ANVISA, 17.09.2019 (Leandro Rodrigues Pereira, General Manager Medical Devices Office, Brazil)

• 09.10.2019

  Regulatory and Policy Updates. Therapeutic Products Directorate. Health Canada, 17.09.2019 (David Boudreau, Health Canada)

• 09.10.2019

  Regulatory update on China Medical Device, 17.09.2019 (Yuan Peng, NMPA, China)

• 09.10.2019

  Update on EU regulatory developments, 19.07.2019 (Erik Hansson, European Commission)

• 09.10.2019

  Japan Regulatory Update, 17.09.2019 (Fumihito Takanashi, MHLW, Japan)

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• 09.10.2019

  New Aspects in Medical Devices Regulation in Russian Federation, 17.09.2019 (Ph.D., Elena Astapenko, Roszdravnadzor, Russia)

• 09.10.2019

  Regulatory Updates. Health Sciences Authority. Singapore, 17.09.2019 (Wong Woei Jiuang, Health Sciences Authority, Singapore)

• 09.10.2019

  Regulatory Updates on Medical Devices in Korea, 17.09.2019 (Jin-young Yang, Ministry of Food and Drug Safety, Korea)

• 09.10.2019

  U.S. FDA Jurisdictional Update, 17.09.2019 (Jeff Shuren, U.S. Food and Drug Administration)

• 09.10.2019

  Regulated Products Submission (RPS). WG Update, 17.09.2019 (Daniel Yoon, Health Canada)

• 09.10.2019

  Adverse Event Terminology and Coding Working Group. Working Group Update, 17.09.2019 (H. Ishikawa, Pharmaceuticals and Medical Devices Agency, Japan)

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• 09.10.2019

  Good Regulatory Review Practices. Working Group Update, 17.09.2019 (Lakshmidevi Balakrishnan, HSA - Singapore, Melissa Torres, US Food and Drug Administration)

• 09.10.2019

  Standards Working Group. Management Committee Update, 17.09.2019 (CAPT Scott Colburn, USPHS)

• 09.10.2019

  Personalized Medical Devices. Working Group Update, 17.09.2019 (Dr Elizabeth McGrath, Department of Health, Australia)

• 09.10.2019

  Medical Device Clinical Evaluation (MDCE). Working Group Update (National Medical Product Administration, China)

• 09.10.2019

  Medical Device Cybersecurity. Working Group Update, 17.09.2019 (Dr. Suzanne Schwartz, US Food and Drug Administration, Marc Lamoureux, Health Canada)

• 09.10.2019

  Principles of In Vitro Diagnostic (IVD) Medical Devices Classification. Working group update, 17.09.2019 (Tatyana Buryakina, Roszdravnadzor)

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• 09.10.2019

  Medical device manufacturing in Russian Federation and harmonization with international practices, 17.09.2019 (Минпромторг России)

• 09.10.2019

  WHO Regulatory Update, 17.09.2019 (Joey Gouws, Group Lead: Inspections)

• 09.10.2019

  Update on Medical Device PWA of RHSC, 17.09.2019 (APEC)

• 09.10.2019

  The Road to Regulatory Harmonization. AHWP Update, 17.09.2019 (Ali Al dalaan, AHWP)

• 09.10.2019

  PAHO Update, 17.09.2019 (Alexandre Lemgruber, PAHO)

• 09.10.2019

  IMDRF Open Stakeholder Forum, 17.09.2019 (Nicole Denjoy, DITTA Chair)

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• 09.10.2019

  Advancing Global Convergence of Medical Technology Regulation, 17.09.2019 (Philippe Auclair, GMTA)

• 09.10.2019

  International certification of medical products: a view of a Russian manufacturer, 17.09.2019 (IAMT)

• 09.10.2019

  Digital Oncology: The role of IT-solutions in early cancer diagnostics, 17.09.2019 (Igor Philippov, Roche Diagnostics Ru)

• 09.10.2019

  Recent Registration Experiences with International Authorities - IVD Perspective, 17.09.2019 (Abbott Laboratories)

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