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    Regulatory Essentials in Health Tech: Compliance as a Business Advantage

    REGULATORY ESSENTIALS

    This session introduces the global regulatory landscape for medical devices and presents the areas health tech developers should focus on when bringing innovations to the markets. Basic terminology, classification rules, and the importance of a regulatory strategy and regulatory due diligence are presented.

    The Regulatory Essentials in Health Tech training series consists of 14 1,5-2 h on-demand webinar sessions.
    Read more on the complete course page here.

    Inhalt

    • Global medical device regulations as your competitive advantage
    • Early focus of the health tech developer
      • Intended Purpose as the heart of your product
      • Is my product a medical device, and what is the risk class? Software, hardware, borderlines
      • What does the risk class tell me about my path to market?
      • How to save resources and time? Avoid re-inventing regulatory compliance
      • Your Regulatory Strategy for market entry
    • Align compliance with your business, marketing, and sales needs
      • General Safety and Performance Requirements at the heart of the regulation
      • Regulatory compliance in your Business Model and Value Proposition
      • The level of regulatory know-how in your business
      • Responsibilities and authorities within the business
      • Regulatory due diligence in investments, mergers & acquisitions – lessons learned
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    Trainer

    Heikki Pitkänen
    Heikki Pitkänen
    CEO & Founder, Lean Entries - Senior Expert, Regulations & Quality
    heikki.pitkanen@aurevia.com
    ”I have more than 20 years of experience in the health tech field including responsibilities in product development as well as regulatory and quality-related positions. I have worked previously at SGS as a site manager providing Medical Device manufacturers with Notified Body, accredited test lab and training services for worldwide market access. I have participated in international standardization and in the CEN-CENELEC Advisory Board for Healthcare Standards."

    Zielgruppe

    All health tech developers and stakeholders interested in gaining crucial knowledge on how to save months in time-to-market of health tech innovations and to avoid typical dead-ends due to non-compliance to the medical device or in vitro diagnostic regulations. Particular focus on start-up founders and staff, university innovator teams, young health tech professionals, business advisors, and investors from early seed development to international scaling.

    Nach diesem Training

    • Have the know-how to apply the correct regulations and standards to your innovation.
    • Understand the most crucial regulatory bottlenecks and typical pitfalls in the health tech business and time-to-market.
    • Recognize the value of understanding the regulatory essentials from early on.
    • Manage the basic terminology of the medical device regulations and standards.

    Hinweis

    Combining this on-demand session with the Regulatory Essentials sessions 2, 3, and 4 is recommended.

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    RECHNUNGS- UND STORNIERUNGSBEDINGUNGEN

    Lesen Sie hier die Abrechnungs- und Stornierungsbedingungen für Online-Schulungen.

    Die Teilnahme an der Schulung kann zwei Wochen (14 Tage) vor der Veranstaltung kostenfrei storniert werden. Bei Stornierungen, die danach erfolgen, berechnen wir 50 % der Teilnahmegebühr, bei Stornierungen, die eine Woche vor der Veranstaltung erfolgen, berechnen wir 100 % der Teilnahmegebühr.

    Stornierungen erfolgen immer schriftlich an: koulutus@aurevia.com.  
    Die teilnehmende Organisation kann den Teilnehmer auf Wunsch kostenlos wechseln, indem sie dies vor der Veranstaltung schriftlich an:  koulutus@aurevia.com meldet. Die Teilnahmegebühr wird unmittelbar nach der Veranstaltung in Rechnung gestellt. Die Trainingseinheit wird dem Teilnehmer ca. eine Woche vor der Veranstaltung per E-Mail bestätigt. Labquality behält sich das Recht vor, die Schulung aufgrund einer zu geringen Teilnehmerzahl abzusagen.