MarketWatch

2 Day Virtual Drug and Biotech Products FDA Regulatory Compliance Training Course: Practical Applications of the Graded Approach in Manufacturing, Testing, and Quality Control ...

The "FDA Regulatory Compliance for Drug and Biotech Products (Nov 12th - Nov 13th, 2025)" training has been added to ResearchAndMarkets.com's offering. Regulatory Compliance is the level of activity ...
C&EN

March 13 Policy Watch: FDA streamlines its process for approving biosimilar drugs

In another development, 25 states have petitioned to join a lawsuit and defend the EPA’s decision to rescind the climate endangerment finding ...
Healthline

The FDA Development and Approval Process for Medications and Medical Devices

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...
Opinion
BioSpaceOpinion

Opinion: Navigating the FDA After the Storm To Advance Drug Candidates

Here’s how drug developers can best approach interactions with the agency following last year’s seismic changes to its leadership, workforce and policies.
National Academies of Sciences%2c Engineering%2c and Medicine

Medical Devices and the Public's Health: The FDA 510(k) Clearance Process at 35 Years

As noted in Chapter 1, the committee was charged by the Food and Drug Administration (FDA) to review the 510(k) clearance process and answer two principal questions: Does the current 510(k) clearance ...