Regulation

Stay updated on MoCRA compliance deadline news today. Learn the new rules for cosmetic adverse event reporting and how to protect your brand and customers.

Get clear, actionable steps for creating an equipment qualification protocol that meets regulatory standards and keeps your manufacturing process compliant.

Learn how to conduct a regulatory gap assessment, spot every regulatory risk gap, and create a clear action plan to strengthen your compliance program.

Understand MoCRA’s new cosmetic facility requirements for FDA registration. Our guide covers deadlines, exemptions, and how to comply. Get the steps you need.

Wondering if you need a consultant for your PMA submission? This guide breaks down the process, from clinical trials to the final checklist. Make an informed choice.

A solid Validation Master Plan (VMP) is crucial for GMP compliance and passing FDA inspections. Get the key components and strategies you need. Learn more now.

Get clear, actionable iso 22716 cosmetics gmp guidance to help your cosmetic business meet global standards for quality, safety, and regulatory compliance.

Ensure FDA compliance for your single-use medical device with simulated use testing. Our guide covers the process for validation and patient safety. Get the details.

Is your recall plan ready for a real crisis? Use our guide to mock recall planning tools to find gaps, improve response time, and safeguard your brand. Get started!

Build a supplier audit program that works. Learn why supplier audit report turnaround time leading service providers is key for quality and compliance.