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Struggling with test methods and specs? See how cGMP Consulting guides dietary supplement makers to confident compliance with 21 CFR Part 111.

Explore what it takes to move from preclinical to clinical, with a focus on cGMP readiness and key challenges to be aware of for a successful transition.

Key questions to evaluate GMP certification readiness, spot gaps, and build a stronger quality system for FDA-regulated industries.

Learn the top FDA observations in dietary supplement manufacturing, how to avoid these compliance issues, and how cGMP Consulting can help you meet 21 CFR Part 111.

Understand 21 CFR Part 111, the cGMP dietary supplement regulations for safe and compliant supplement manufacturing.

Discover how cGMP compliance helps distributors access regulated industry opportunities by ensuring quality and building trust. Let cGMP Consulting help!

Learn key steps to conduct effective internal audits, ensure FDA compliance, and boost operational efficiency in 2025. Stay ahead with expert tips.

Explore GMP vs. cGMP, their key differences, principles, and benefits, and understand why staying 'current' is essential for regulatory compliance and manufacturing success.

Learn the key differences between GMP and cGMP, why compliance matters, and how to implement cGMP for regulatory success. Stay competitive and compliant with this essential guide.

Get essential insights on FDA and GMP compliance to help your business meet regulatory standards effectively.

This guide covers the fundamentals of Good Manufacturing Practices (GMP), the 10 key elements for compliance, the GMP process, best practices, and FDA inspection insights.

Learn how a food and OTC manufacturer successfully resolved an FDA warning letter and improved their compliance practices.

Discover practical strategies to avoid FDA 483 observations and ensure seamless compliance in your industry.

Prevent FDA 483 issues with expert strategies in compliance, data integrity, and quality systems from cGMP Consulting.

Understand the financial and operational risks of receiving an FDA 483 and how to prevent compliance issues.

Discover immediate actions to take after receiving an FDA 483 and prevent further compliance issues.

Prepare your organization for success with cGMP Consulting's Audit Readiness Training. Our 5-step process equips your team to excel in regulatory inspections.

Prepare for MoCRA GMP compliance with cGMP Consulting. Get expert help with assessments, SOPs, and training for early compliance and reduced risks.

Discover how to seamlessly implement electronic GMP systems with expert consulting from cGMP Consulting and amni.ai. Enhance compliance and operational efficiency in FDA-regulated industries.

Explore the essential elements of cosmetic GMPs and learn how cGMP Consulting can help ensure the safety, efficacy, and quality of your cosmetic products while navigating regulatory compliance.

Your essential guide to MoCRA compliance. Discover the latest regulations and steps to ensure your cosmetics meet FDA standards. Start preparing today!

Master the GMP certification process with cGMP Consulting’s ultimate guide. Learn about our comprehensive evaluation, certification recommendations, and ongoing compliance support.

Facing challenges in GMP certification? Learn about the top obstacles and expert tips to achieve compliance in regulated industries.

Elevate your quality standards with cGMP Consulting's GMP Certification Audits. ISO/IEC 17020:2012 accredited, we offer tailored audits for compliance and quality assurance.

Master GMP compliance with cGMP Consulting's comprehensive auditing services. Explore 8 tailored solutions to enhance product quality, ensure regulatory adherence, and build market trust.