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EUCROF Code of Conduct for Service Providers in Clinical Research
Please complete this form to receive the documents of the Code by email
Name *
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Position in the Company
Purpose of your interest in the EUCROF GDPR Code of Conduct *
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CRO / Service Provider for clinical research
Healthcare Professional involved in clinical research
Patient participating in a clinical study
Patients advocacy group
Company / organization sponsoring clinical studies
Private data privacy specialist - DPO - Legal consultant
Public organization / Institution
Other
Are you a CRO candidate for adherence to the EUCROF GDPR Code of Conduct?
Are you:
a health care professional
involved in clinical research
working as data protection officer
a consultant on regulatory issues
More details about your request/interest (as needed)
By submitting this request, you authorize EUCROF to use your email address for further communications and updates on Code of Conduct news and other EUCROF events (webinars, annual conference on clinical research). You can cancel receiving such information at any time by sending a request at
info@eucrof.eu
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