Apologies to Luke Bryan (or maybe Luke Bryan should apologize to us?), but after you read this you’ll be less likely to think that “Most People Are Good.” Accenture recently released survey results from 912 employees of provider and payer organizations in the US and Canada. They found 18% of respondents would be willing to sell confidential data to unauthorized parties for as little as $500 to $1,000. What the…? Remember, these are employees of provider and payer organizations. 21% said they keep their user name and password written down next to their computer. C’mon Man. It gets worse when we move from hypothetical to reality where “24% of respondents said they know of someone in their organization who has sold their credentials or access to an unauthorized outsider.” To the 18% – “you’re just a bad person, all the way through to your core.”
Would you consent to your physician audio recording your visits?
Apparently, pharma companies, CROs, and universities will have new EU privacy rules to contend with in about eight months. Great. The EU’s General Data Protection Regulation (GDPR) applies to all types of data, but it will have a special impact on clinical trials. According to Debra Diener, an attorney and Certified Information Privacy Professional. “Sensitive data now includes, under this regulation, genetic data, biometric data, that is a broader set of data than is covered by HIPAA.” InsightCity has to ask, if you’re a US-based pharma company or CRO, why conduct trials in Europe, why risk it? That said, the informed consent process definitely needs an overhaul. The GDPR indicates the IC must be unambiguous, with affirmative action by the individual. Hard to argue with that. So, sharpen your regulatory pencils and get ready.