Today, the FDA debuted a new page on their website called Upcoming Product-Specific Guidances for Complex Generic Drug Product Development. Its stated purpose is to provide “information related to upcoming new and revised product-specific guidances (PSGs) to support the development and approval of safe and effective complex generic drug products.” This comes after several public […]
Well, our unofficial projections got the full approval actions right (at 55) but we missed one tentative approval action that was posted late (we reported 16) (here) but the official total reported here actually tallied 17 for a total of 72 approval actions for April 2021. 11 of the 55 full approvals were for first-time […]
The FDA will publish a notice in the Federal Register tomorrow (May 13, 2021) that announces a notice of intent to scope out the need to issue an environmental impact statement relative to certain sunscreen active ingredients (namely oxybenzone and octinoxate) and their potential impact on the health of the coral reefs. This notice of […]
Covering a multitude of subjects, the Agency published eight new guidance documents ranging from the ICH M9 BCS classification system to a Q&A document on qualified infectious disease designations. Here is a list of the eight guidance documents. M9 Biopharmaceutics Classification System-Based Biowaivers (here) E9(R1) Statistical Principles for Clinical Trials: Addendum: Estimands and Sensitivity Analysis […]
The Office of Generic Drugs (OGD) provided the final set of metrics to complete the March 2021. While many of the numbers are consistent with other months of this FY, there are a couple of surprise figures which we will cover, and will provide our commentary in an effort to try to explain them. There […]
Just nine (9) days ago, I posted a blog and article (here) on the issue of paper prescribing information – package inserts! The overall takeaway was that FDA is ready to move on this issue. There was a proposed rule sitting dormant, because every year since its proposal, e Congress has included a provision in […]
As the pandemic approaches its latter stages, it has been more than a year since medical device industry leaders and executives have been able to get together in person at conferences and gatherings to share information and experiences. Opportunities to have virtual events of the same nature have been rare as well. One of those […]
While there still may be a few more stragglers that have not yet hit the FDA’s “All Approvals List” as of May 6, 2021 (here), we will catch them when the OGD releases its official numbers for April sometime in the next two weeks. The total for full- and tentative-approval actions reported was 71 which, if […]
The ANDA suitability petition process has been languishing for years. Over the years, we have drafted many posts (here, here, here, here, here, here, here, and here, among others) regarding the FDA’s failing to act on what is a statutorily mandated ninety-day time period for approving or denying an ANDA suitability petition. Today, I read […]
Do you ever wonder why the minutes of the PDUFA and GDUFA user-fee negotiation sessions are so scant? Minutes of one-hour meetings with the drug companies are typically two to five pages at the least, depending on the topics discussed. Transparency for the drug UFA negotiation meetings appears to be somewhat lacking (see previous post […]
