ABOUT GMP CERTIFICATION IN CANADA

A Good Manufacturing Practices (GMP) certificate verifies and certifies that standards for a successful Hazard Analysis Critical Control Point (HACCP) food safety program are being followed. “Good Manufacturing Practices” is what the “GM” in “GMP” stands for. The FDA uses it to verify that foods are safe for customers and to “improve food safety control at all phases of manufacturing, processing, distribution, and consumption.”

The Difference Between GMP and cGMP

GMP is also known as “cGMP,” with the “c” standing for “current,” according to another source. The letter “c” should be written in small characters since it denotes perpetual change and the ever-evolving technology of excellence. This serves as a reminder to producers that they must use cutting-edge technology.

How to Prepare your Organization for GMP Certification in Canada

The following are helpful tips to prepare your organization for GMP certification in Canada:

  1. Choose the best GMP standard for your product and company.
  2. Recognize what is required to establish, maintain, and demonstrate GMP compliance.
  3. Determine which management systems are required to ensure that your facility, processes, and products comply with GMP certification requirements.
  4. Confirm that all employees are completely aware of and understand their obligations in terms of GMP compliance and the required work processes.
  5. Identify any current GMP non-compliance issues.
  6. Apply, register, and have your business examined by IAS for GMP certification in Canada.

Steps to Obtain GMP Certification in Canada

Once your organization has prepared for GMP certification, follow these steps to get certified:

  1. A GMP-compliant manufacturing facility and personnel with prior expertise are required.
  2. Conduct a risk-based audit of your GMP processes.
  3. Receive answers to your questions about GMPs from the FDA.
  4. Within 90 days following the audit, plan corrective action for all non-compliant areas/aspects.
  5. Within 120 days following the audit, implement the corrective actions.
  6. Ensure that corrective actions are carried out according to plan and that no issues are left ignored at any time.