Tag Archives: investigator-sponsor

GDPR: DOES IT IMPACT YOUR CLINICAL STUDY?

It is hard to miss, but as of May 25, 2018, the GDPR becomes effective. Although collection and review of personal data and clinical studies have gone hand-in-hand for decades and therefore I do not expect major changes, the devil … Continue reading

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INVESTIGATOR CLINICAL STUDIES: FOUR KEY THINGS TO DO

Last week some-one asked me what it is that industry can and can not do in investigator initiated trials (IITs). The challenge in answering this question goes back to the question who the sponsor – and therefore the one being … Continue reading

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