BEGIN:VCALENDAR VERSION:2.0 PRODID:-//CiviCRM//NONSGML CiviEvent iCal//EN X-WR-TIMEZONE:Europe/London METHOD:PUBLISH BEGIN:VTIMEZONE TZID:Europe/London BEGIN:DAYLIGHT TZOFFSETFROM:+0100 TZOFFSETTO:+0100 TZNAME:BST DTSTART:20260602T140000 END:DAYLIGHT END:VTIMEZONE BEGIN:VEVENT UID:CiviCRM_EventID_95_3b79d502593e3d7f92580130e54fd34a@www.ephmra.org SUMMARY:Webinar: Compliance Made Practical: Reviewing the Legal Bases for Healthcare Market Research X-ALT-DESC;FMTTYPE=text/html:

Healt hcare market research is evolving rapidly. Global studies\, AI-powered platforms\, and new technolog y providers are transforming how research is deliv ered – while privacy regulations across jurisdicti ons continue to create challenges for multi-countr y research.

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This webinar will provide a prac tical review of the legal bases available\, explor e how they are applied differently across jurisdic tions\, and demonstrate why informed consent remains the most practical and ethically robust foundation for healthcare market research.

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The webinar will:

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Provide a clear overview of the legal bases u sed for personal data processing across major glob al privacy frameworks
Exami ne how consent\, legitimate interest\, and other b ases are treated differently across jurisdictions – and what this means for multi-country research

Present why informed consent is recommended as best practice\, supporting tran sparency\, voluntary participation\, and cross-bor der compliance\n
Highlight th e importance of embedding compliance into technolo gy and platform design from the outset
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\n \n Target Audience

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This webinar is d esigned for professionals in:

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Pharmaceutical\, Diagnostics and Medic al Devices companies
Market Research agencies
Technolo gy/Platform providers supporting healthcare market research

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It is particularly releva nt for professionals working in:

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Compliance & Privacy
Research operations
Fieldwork and panel management
Technology development

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Ke y Takeaways for Attendees

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Understand how legal bases differ acro ss global privacy frameworks\, particularly for al l the personal data processed in healthcare market research.
Learn why infor med consent is the practical and ethical "gold sta ndard" – and when alternatives may apply
Recognise the importance of building privacy and compliance into research platforms an d new product solutions from the outset.

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Speakers: Matt eo Cappai\, Director\, Co-Head of Healthcare Compl iance\, Ipsos and Sarah-May Hall\, Managing Direct or\, Zeste Health

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Convenor : Georgina Butcher\, EPHMRA Ethics Consul tant

DESCRIPTION:Healthcare market research is evolving rapidly. Gl obal studies\, AI-powered platforms\, and new tech nology providers are transforming how research is delivered – while privacy regulations across juris dictions continue to create challenges for multi-c ountry research.\n \n \n \n This webinar will prov ide a practical review of the legal bases availabl e\, explore how they are applied differently acros s jurisdictions\, and demonstrate why informed con sent remains the most practical and ethically robu st foundation for healthcare market research.\n \n \n \n \n \n \n \n The webinar will:\n \n \n \n \ n Provide a clear overview of the legal bases use d for personal data processing across major global privacy frameworks\n Examine how consent\, legit imate interest\, and other bases are treated diffe rently across jurisdictions – and what this means for multi-country research\n Present why informed consent is recommended as best practice\, support ing transparency\, voluntary participation\, and c ross-border compliance\n Highlight the importance of embedding compliance into technology and platf orm design from the outset\n \n \n Target Audience \n \n \n \n This webinar is designed for professio nals in:\n \n \n \n \n Pharmaceutical\, Diagnosti cs and Medical Devices companies\n Market Researc h agencies\n Technology/Platform providers suppor ting healthcare market research\n \n \n It is part icularly relevant for professionals working in:\n \n \n \n \n Compliance & Privacy\n Research oper ations\n Fieldwork and panel management\n Techno logy development \n \n \n Key Takeaways for Attend ees\n \n \n \n \n Understand how legal bases diff er across global privacy frameworks\, particularly for all the personal data processed in healthcare market research. \n Learn why informed consent i s the practical and ethical "gold standard" – and when alternatives may apply\n Recognise the impor tance of building privacy and compliance into rese arch platforms and new product solutions from the outset.\n \n \n Speakers: Matteo Cappai\, Director \, Co-Head of Healthcare Compliance\, Ipsos and Sa rah-May Hall\, Managing Director\, Zeste Health \n \n \n \n Convenor: Georgina Butcher\, EPHMRA Et hics Consultant\n \n CATEGORIES:Webinar CALSCALE:GREGORIAN DTSTAMP;TZID=Europe/London:20260602T140000 DTSTART;TZID=Europe/London:20260602T140000 DTEND;TZID=Europe/London:20260602T143000 LOCATION:Online Event\n URL:https://www.ephmra.org/civicrm/event/info?reset=1&id=95 END:VEVENT END:VCALENDAR