GMP Manual Update
GMP Manual Update for Cosmetics Manufacturers in the USA
As the FDA enforces new requirements through the Modernization of Cosmetics Regulation Act (MoCRA), U.S. cosmetic manufacturers must ensure their Good Manufacturing Practices (GMP) are documented, traceable, and up to date.
One essential step in this process is maintaining a compliant, well-structured GMP manual—a critical tool for demonstrating operational quality and regulatory alignment.
At Sobel, we help cosmetic companies revise and update their GMP manuals to meet current U.S. expectations, including those introduced by MoCRA. Our service results in documentation that reflects real practices, supports internal audits, and is structured to meet regulatory expectations.
How we support your GMP Manual Update
Our service is designed to modernize your company’s GMP documentation for cosmetic manufacturing, aligning your manual with MoCRA and FDA requirements while keeping it practical for day-to-day use.
The process includes:
Document gathering: Collection of all previous GMP manual versions and supporting documents;
Structural review: Evaluation of how content is organized, ensuring logical flow and traceability;
Regulatory updates: Revision of regulatory references, adapting content to reflect current MoCRA GMP compliance expectations;
Operational process review: Validation and adjustment of procedures related to production, quality control, hygiene, and storage;
Employee training evaluation: Review of training records and integration of training protocols into the manual where needed;
CAPA review: Assessment of Corrective and Preventive Action (CAPA) procedures to verify they meet best practices;
Final review and approval: Delivery of a complete, ready-to-implement GMP manual reflecting your company’s updated processes.
We don’t just revise documents—we help you align your GMP system with evolving U.S. cosmetic manufacturing compliance standards.
Why do you need this service?
The new law requires manufacturers to follow and document GMP principles.
A well-structured manual supports FDA inspections and internal audits by clearly documenting your processes.
Reviewing and revising your GMP content offers an opportunity to optimize workflows and reinforce best practices.
We specialize in helping companies adapt to changing regulations without disrupting daily operations. Our team works alongside your staff to ensure your GMP manual update is efficient, accurate, and aligned with both MoCRA and FDA expectations.
Whether you need a complete revision or targeted updates, we deliver structured, compliant documentation that reflects your current reality and supports future audits.
Need to update your GMP Manual for MoCRA Compliance?
Let us help your team stay one step ahead. With Sobel’s support, your cosmetic facility’s GMP documentation will be ready to meet today’s standards and tomorrow’s challenges.
Contact us to learn more about our GMP manual update services for the U.S. cosmetics industry.
