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Good Clinical Practice (GCP)
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Computerized System Validation (CSV)
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ICH GCP E6(R3)
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"Beyond the Signature: What ICH GCP R3 Really Means for Site and Sponsor Oversight"
Webinar Registration Form
3-Minute Participant Survey
Required for participation in:
Webinar "Beyond the Signature: What ICH GCP R3 Really Means for Site and Sponsor Oversight"
May 30, 2025 | 18:00 CEST | Live session with Q&A
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Your role:
Sponsor or Sponsor Representative
CRO or Service Provider
Investigator or Site Staff
Other (Regulatory, EC, Consultant, etc.)
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Have you already started preparing for E6(R3)?
Yes
Not yet
Not applicable
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How is GCP or regulatory training usually organized in your team?
We purchase external courses individually
We train internally using our own materials
We buy external training only for key staff (e.g., QA, PMs)
We don’t have a structured approach — decisions are ad hoc
Not applicable
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What is the main challenge you face when choosing a training on ICH GCP E6(R3)? (Select up to 2)
Lack of time to complete long programs
Unclear value or return on investment
Not sure which provider to trust
Lack of budget or internal approval
Already have internal training
Still waiting for implementation / not urgent
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