Medical Cannabis

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Medical cannabis products require the same rigorous approach to quality, manufacturing, and regulatory compliance as any other healthcare product. GSAP supports companies across cultivation, manufacturing, quality systems, validation, and regulatory activities, helping them operate with confidence in a rapidly evolving market.

Canabis

How We Support Medical Cannabis Companies

 

  • Regulatory Strategy & Global Market Requirements
    Development of regulatory strategies, submission pathways, and regulatory documentation for cannabis-derived products, including support for market-specific requirements and regulatory authority interactions
  • Medical Cannabis Quality Systems
    Implementation and maintenance of Quality Management Systems (QMS) supporting medical cannabis activities in accordance with applicable GMP, GDP, and industry-specific quality requirements
  • Facility Compliance & Manufacturing Readiness
    Support for cultivation, processing, post-harvest, manufacturing facilities and wholesalers through facility compliance assessments, GMP readiness activities, and operational quality frameworks
  • Audits, Inspection Readiness & Data Integrity
    Mock inspections, compliance audits, data integrity assessments, supplier audits, subcontractor qualification, and inspection readiness programs
  • Product Quality & Specifications
    Support for product specifications, analytical requirements, quality documentation, and consistency programs supporting medical cannabis products
  • Clinical Development & Regulatory Support
    Strategic support for clinical development activities, clinical trial preparation, regulatory submissions, and interactions with health authorities related to cannabis-based products
  • Cannabis Qualified Person (CQP) Services
    Support for Cannabis Qualified Person (CQP) certification, batch release activities, and related quality oversight programs