Deconstructing CBER’s Web-Posting Mandates for PMAs and HDEs 

Navigating the regulatory clearance process for high-risk medical devices within the Center for Biologics Evaluation and Research (CBER) extends beyond securing an approval or denial order. Once a decision is rendered, regulatory affairs professionals must oversee the post-action administrative workflows that dictate public transparency. CBER’s Standard Operating Policy and Procedure (SOPP) 8795 establishes the internal mechanisms governing public … Read more

Is Industry Funding Really Poisoning Science? The Overlooked Guardrails of Modern Trials 

Financial conflict of interest in medical research is a topic that instantly draws headlines, skepticism, and heated academic debates. A recent study published in JAMA Network Open reignited this fire by pointing out that nearly 90% of industry-funded trials report conclusions favoring their corporate sponsors. To many observers, that statistic sounds like smoking-gun evidence that commercial money corrupts scientific … Read more