Site Audit

A site inspection should be conducted periodically to ensure that your manufacturing, packaging, labeling, importing, or distribution center complies with Health Canada regulations.

A site audit is a standardized process utilized by experts to determine whether you are complying with Health Canada and FDA standards in manufacturing, packaging, labeling, and distributing products. A site audit or site inspection brings a pristine faction of eyes to assess your logs and procedures and discover where there are deficiencies. With a site inspection checklist, our site audit specialists will have a look at your site and compile a site audit report to outline deficiencies, areas of improvement and recommendations. 

A site audit helps to ensure that your manufacturing, packaging, labeling, importing, or distribution facility properly documents all activities consistently, practices due diligence in all areas, and meets the regulations set by the regulatory body. We will work as your site audit specialist to provide a personalized, walk-through inspection of your facility.

1. Standard Operating Procedures (SOPs)
2. Good Manufacturing Practices (GMP) Records
3. Data logs
4. Certificates of Analysis and Batch Production Records