Posts by Becca DuBose

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FDA to host Pediatric Medical Devices Workshop

FDA’s Office of Orphan Products Development recently announced a public educational workshop to be held September 24, 2012 in Silver Spring, MD. The workshop, which[…]

House subcommittee votes to cut DHHS budget, defund AHRQ

The US Department of Health and Human Services budget would be cut by $1.3B, and funding for the Agency for Healthcare Research and Quality would[…]

AEs, SAEs, and UPIRTSOs…Oh My!

Numerous terms, all with subtle differences in meaning, are used to refer to the undesirable occurrences commonly referred to as adverse events. An article in[…]

AEs, SAEs, and UPIRTSOs…Oh My!

Numerous terms, all with subtle differences in meaning, are used to refer to the undesirable occurrences commonly referred to as adverse events. An article in[…]

Unnecessary Procedures Add Costs and Complexity to Clinical Trial Protocols

A study by Medidata Solutions suggests that up to 20% of clinical trial budgets go to pay for procedures that are not directly related to[…]

Regulatory Updates from FDA and OHRP

FDA is currently seeking public comments regarding its Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens that are Not Individually[…]

NIH Considers Educational Video Game

According to a notice in today’s Federal Register, the National Institutes of Health (NIH) is seeking public comments on a proposed video game to educate adolescents[…]

DSMBs: Are They Working As Intended?

An article by Matthew Herper of Forbes.com raises questions about the independence of data safety monitoring boards (DSMBs), and the potential for trials of promising[…]

Do All Patients Really Have Equal Access to Clinical Trials?

According to research presented earlier this week at the annual meeting of the American Society of Clinical Oncology, an annual income of less than $50,000[…]

Pharma Companies Make Recommendations to Enhance Credibility of Clinical Trial Publications

A group of pharmaceutical companies has issued a list of recommendations for improving the transparency and credibility of industry-supported clinical research. The recommendations include: Making all[…]