GMP Compliance.

As a professional consulting firm, we specialize in providing Good Manufacturing Practices (GMP) compliance services for companies seeking Health Canada approvals. Our mission is to guide businesses through the intricate regulatory landscape, ensuring their products meet the highest quality standards.

What Are Good Manufacturing Practices (GMP)?

Good Manufacturing Practices (GMP) are essential guidelines that ensure drugs and health products are manufactured, packaged, and labelled in compliance with quality standards before they are sold. Health Canada inspects establishments involved in drug fabrication, packaging, labelling, testing, distribution, import, and wholesale to verify GMP compliance1.

Why Choose Us?

  1. Regulatory Mastery: We understand Health Canada’s evolving requirements, ensuring your compliance.
  2. Efficiency: We streamline the application process, minimizing delays.
  3. Client-Centric Approach: Your success is our priority. Let’s collaborate to achieve Health Canada approvals.


Our Expertise

  • Pharmaceuticals: We have in-depth knowledge of Health Canada, the U.S. Food and Drug Administration (FDA), and European Medicines Agency (EMA) regulations. Our team assists with GMP compliance for pharmaceuticals intended for sale in Canada.
  • Natural Health Products (NHPs): Whether it’s over-the-counter (OTC) drugs or NHPs, we ensure GMP compliance throughout the product lifecycle.
  • Active Pharmaceutical Ingredients (APIs): Our expertise extends to APIs, ensuring they meet GMP requirements.
  • Quality Assurance: We provide strategic guidance on ISO 13485 for medical devices and pharmacovigilance GMPs.

Get Started Today:

Ready to take the next step in bringing your natural health product to the market? Contact Bridge Compliance today. We’re here to provide you with the guidance, expertise, and support at Canada. Let’s bridge the gap together and make your product a success!