The FDA has posted a Request for Comments to better understand how to regulate software developed by drug sponsors for use with their prescription drugs (Docket No. FDA-2018-N-3017). The request notes that sponsors who have been developing software apps to market with...
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Source Code and Technical Documents for a Clinical Trials App
In early November, the FDA announced they were releasing the open source code and technical information for their MyStudies app. This app was developed and piloted by the FDA as a way for patients enrolled in a clinical trial to enter their own health data which would...
Next Generation Sequencing – will it work for MRD?
In an earlier post I noted that pathology experts believe next generation sequencing will be required to bring minimal residual disease (MRD) into focus as a more valuable endpoint for clinical trials of leukemia treatments. I’ve reviewed the technique, which starts...
Katrina’s Reading List
Understanding How We Make Decisions Many people ask me for professional advice on making a decision, to which question there is seldom a short answer. To prepare for such questions, I recommend reading widely about the science behind our decision-making processes....
The Orange Book is Available as an App
The Orange Book is the common name for the FDA publication “Approved Drug Products with Therapeutic Equivalence Evaluations”. This reference work contains lists of drug products approved by the FDA, and its purpose is to enable providers and patients find substitute...
CDRH Guidance Schedule for FY2019
CDRH has published a list of guidance documents that the division intends to publish or review in FY2019. There are 3 separate parts to the list:The “A list”, guidance documents that the division intends to publish,The “B list”, guidance that will be published as...
Genetic Testing to Predict Medication Response
– what has and hasn’t been reviewed and approved Genetic testing to enhance patient outcomes is a hot topic in the news this year, and the FDA plays a role in reviewing and approving such tests for use. Some of the claims made by providers have not been reviewed by...
MRD as a Biomarker in Clinical Trials for Leukemia
– draft guidance comment period ends 15DEC2018Interested parties have about a month to comment on the draft guidance for those planning to use minimal residual disease (MRD) as a biomarker in oncology clinical trials for treatment of blood diseases. Released in...