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  • Testing Confusion to Compliance Confidence | 21 CFR Part 111

    From Testing Confusion to Compliance Confidence: How Our Experts Help Supplement Manufacturers Meet cGMP Standards

    June 3rd, 2025Dietary Supplements, Industry Expertise, Regulatory Response

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

    Read More
  • Trends and How They Impact Supplement Manufacturing

    Six Emerging Trends and Their Influence on Dietary Supplement Manufacturing Practices

    April 7th, 2025Dietary Supplements, Industry Expertise, Regulatory Response

    Learn how six key trends are reshaping dietary supplement manufacturing and 21 CFR Part 111 compliance across the industry.

    Read More
  • Top FDA Observations in Dietary Supplement Manufacturing

    Top Two FDA Observations in Dietary Supplement Manufacturing: How to Avoid Them

    March 10th, 2025Dietary Supplements, Industry Expertise, Regulatory Response

    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.

    Read More
  • FDA GMP Compliance

    FDA and GMP Compliance: What You Need to Know

    November 26th, 2024Industry Expertise, Regulatory Response

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

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  • Resolving an FDA Warning Letter

    Success Story: Resolving an FDA Warning Letter for a Food & OTC Manufacturer

    November 18th, 2024Industry Expertise, Regulatory Response

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

    Read More
  • FDA 483 Observations

    Avoiding Common FDA 483 Observations: An Industry-Specific Compliance Guide

    November 6th, 2024Industry Expertise, Regulatory Response

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

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  • Driving Continuous Improvement in FDA-Regulated Industries: Strategies to Prevent FDA 483 Issues

    Driving Continuous Improvement in FDA-Regulated Industries: Strategies to Prevent FDA 483 Issues

    October 21st, 2024Industry Expertise, Regulatory Response

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

    Read More
  • Cost of FDA 483

    The True Cost of Receiving an FDA 483: A Breakdown of Financial and Operational Risks

    October 14th, 2024Industry Expertise, Regulatory Response

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

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  • Immediate Steps to Take After Receiving an FDA 483: Don’t Risk a Warning Letter

    Immediate Steps to Take After Receiving an FDA 483: Don’t Risk a Warning Letter

    October 7th, 2024Industry Expertise, Regulatory Response

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

    Read More

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Logo cGMP Consulting Inc.

cGMP Consulting has helped clients stay compliant with the current Good Manufacturing Practices (cGMP) and implement new technologies since 2001.

We are ISO accredited and perform GMP Certification Audits.
cGMP Consulting Inc.

580 N Bank Lane

Lake Forest, IL 60045

Phone:1 (312) 420-7682

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