Services

Canna Consulting 420 is a professional cannabis and cannabinoid consulting firm offering high-level regulatory experience for guiding businesses in manufacturing compliance. We provide expertise in key areas such as good manufacturing practices, product development, quality management, documentation, packaging, labeling, holding operations, analytical and laboratory testing, employee training, extractions, infusions and sustainability.

INITIAL CONSULTATION:
EVALUATION & DISCOVERY
  • Current Operations Review

  • Discuss Business Plans & Systems Control Goals

  • Identify Short-term & Long-term Quality Management Goals

  • Meet With Quality Team & Define Individual Roles

  • Identify Problem Areas & Concerns

  • Prioritize Compliance Needs

  • Establish Timeline to Inspection Readiness

  • Discuss Corporate Culture

QUALITY MANAGEMENT
  • Quality Systems Planning & Guidance

  • Further Review of Current Operations & Problem Areas

  • Define Quality Management QA/QC/QU Responsibilities

  • Determine Staffing, Education & Training Needs

  • Employee Training Manual Review & Development

  • Create a Corporate Culture for Quality & Compliance

  • Identify & Implement Regulatory Policies

  • Evaluate Inventory Systems & Management

  • Process Control Management

  • Safety Management

  • Security Requirements

MANUFACTURING & DISTRIBUTION
  • Good Manufacturing Practices Overview

  • Operations & Manufacturing Appraisal

  • Evaluate Compliance and Regulatory Needs

  • Review Policies, Procedures & Best Practices

  • Quality Assurance Systems Review

  • Analyze Manufacturing Safety Controls

  • Processing & Workflow Procedures

  • Labeling & Packaging Requirements

  • Supplier Qualification & Supply Chain Management

  • Quality Control Testing System (Internal & External Lab)

  • Materials Management (Storage, Holding & Transport)

DOCUMENTATION SYSTEMS:
ESTABLISH, REVIEW & REVISE
  • Policies and Procedures

  • Standard Operating Procedures (SOP)

  • Master Manufacturing Records (MMR)

  • Specifications (SP)

  • Forms, Logs & Worksheets

  • Change Control Systems (CC)

  • Out of Specification (OOS) Investigations, Documentation & Resolution

  • Product Complaints & Adverse Event Reporting (AER)

  • Record Keeping Requirements

  • Organization & Access Control of Documents

  • Employee Training on SOP/MMR/BR/SP/CC/Forms

INSPECTION READINESS
  • Develop & Refine Audit Process

  • Site Inspection & Preparation Checklist

  • Mock Recall Program

  • Internal Audit Procedures

  • Facility Design (Limited Access Areas/Signage/Security)

  • Pest Management Controls

  • Independent 3rd Party Auditing

  • Procedures for Audits by Governing Regulatory Agencies

CONTINUOUS IMPROVEMENT
  • Quality Program Review

  • Future Planning & Guidance

  • Self-Auditing

  • Systems Review

  • Document Revision

  • Mock Recalls

  • Ongoing Staff Trainings

  • Strengthening Quality Culture

  • Positioning for Growth