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6 in total

Review 1. Postmarketing surveillance for "modified-risk" tobacco products.

Authors: Richard J O'Connor
Journal: Nicotine Tob Res Date: 2011-01-20 Impact factor: 4.244

2. Medical device postapproval safety monitoring: where does the United States stand?

Authors: Prashant V Rajan; Daniel B Kramer; Aaron S Kesselheim
Journal: Circ Cardiovasc Qual Outcomes Date: 2015-01-06

3. FDA regulation of cardiovascular devices and opportunities for improvement.

Authors: Sanket S Dhruva; Rita F Redberg
Journal: J Interv Card Electrophysiol Date: 2012-12-21 Impact factor: 1.900

4. Improving medical device regulation: the United States and Europe in perspective.

Authors: Corinna Sorenson; Michael Drummond
Journal: Milbank Q Date: 2014-03 Impact factor: 4.911

Review 5. Post-market surveillance to detect adverse events associated with Melody® valve implantation.

Authors: Kevin D Hill; Bryan H Goldstein; Michael J Angtuaco; Patricia Y Chu; Gregory A Fleming
Journal: Cardiol Young Date: 2016-11-10 Impact factor: 1.093

6. Medical-device recalls in the UK and the device-regulation process: retrospective review of safety notices and alerts.

Authors: C Heneghan; M Thompson; M Billingsley; D Cohen
Journal: BMJ Open Date: 2011-05-15 Impact factor: 2.692

6 in total