510K
AA
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ITA
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JP
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Premarket Notification (US)
Atomic Absorption
Alberta Blue Cross
Atlantic Pharmacare Review Committee
Adverse Reaction
American Society for Quality
Access to Information
Batch Certificate
Biologics and Genetic Therapies Directorate
British Herbal Pharmacopeia
British Pharmacopeia
Canadian Agency for Drugs and Technologies in Health
Certified Biomedical Auditor
Certified Calibration Technician
Comparative Drug Index 
Common Drug Review
Common Drug Review
Controlled Drugs and Substances Act
Canadian Expert Drug Advisory Committee
Canadian Environmental Protection Act
Canadian Formulary
Canadian Food Inspection Agency
Certified HACCP Auditor	
Council for International Organizations of Medical Sciences
Chemistry, Manufacturing and Controls
Canadian Medical Device Conformity Assessment System
Cosmetic Notification
Certificate of Analysis
Certificate of Manufacturer
Certified Product Information Document
Certificate of Pharmaceutical Product
Compendium of Pharmaceuticals and Specialties 
Certified Quality Auditor
Canadian Reference Product
Canadian Standards Association
Clinical Trial Application
Clinical Trial Application Amendment
Common Technical Document
Drug Identification Number
Drug Identification Number 
Drug Identification Number Biologics
Drug Identification Number Disinfectants
Drug Identification Number (Category IV)
Dealer’s License (Dealer’s Licence)
Drug Master File
Drug Notification Form
Drug Product Database
Drug Quality Assessment Committee
Drug Quality and Therapeutics Committee
Domestic Substances List
Economic Council of Canada
Electronic Common Technical Document
Establishment License (Establishment Licence)
Food and Drugs Act
US Food and Drug Administration
Food and Drug Regulations
Failure Mode and Effect Analysis
Gap Analysis
Gas Chromatography
Good Clinical Practices
Good Laboratory Practices
Good Manufacturing Practices
Hazard Analysis and Critical Control Points
Health Canada
Healthy Environments and Consumer Safety
Health Protection Branch
Health Products and Food Branch 
Health Products and Food Branch Inspectorate
High Performance Liquid Chromatography
Investigator’s Brochure
International Conference on Harmonisation
International Nomenclature of Cosmetic Ingredients
Investigational New Drug Submission
International Organization for Standardization
Investigational Testing Application
In Vitro Diagnostic Device
Japanese Pharmacopeia
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NHPD
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NIDPF
NMI
NOC
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NOD
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NPN
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SI
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SL
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TPD
USP
VDD
vNHP
WHO

Market Access
Medical Device
Medical Devices Bureau
Medical Device Establishment Licence
Medical Device Regulations
Manitoba Drug Standards and Therapeutic Committee
Marketed Health Products Directorate
Medicinal Ingredient
Mandatory Problem Report
Material Safety Data Sheet
National Association of Pharmaceutical Regulatory Affairs
New Brunswick Prescription Drug Program Formulary
New Brunswick Product Selection Committee 
Notifiable Change
National Coordination Centre
New Drug Submission
National Drug Scheduling Advisory Committee
National Formulary
Natural Health Product
Natural Health Products Directorate
Natural Health Product Regulations
Newfoundland and Labrador Interchangeable Drug Products Formulary
Non-Medicinal Ingredient
Notice of Compliance
Notice of Compliance with Conditions
Notice of Deficiency
No Object Letter
Notice of Noncompliance – Withdrawn
Natural Product Number
Not Satisfactory Notice
New Substances Notification Regulations
Office of Controlled Substances
Ontario Drug Benefit Formulary
Over the Counter
Pharmaceutical Advertising Advisory Board
Process Failure Mode and Effect Analysis
European Pharmacopeia
Pharmaceutical Inspection Cooperation Scheme
Product Licence Application
Product Monograph
Patented Medicines Prices Review Board
Pest Management Regulatory Agency
Product Safety Update Report
Quality Assurance
Quality Assurance Person
Quality Assurance Report
Quality Control
Quality Information Summary – Biologics
Quality Information Summary – Pharmaceuticals
Quality Management System
Quality Overall Summary – Chemical Entity
Quality Overall Summary
Quality Overall Summary – Bioequivalence Study
Qualified Person in Charge
Quality System Inspection Technique
Quality System Regulations
Regulatory Affairs
Regulatory Affairs Certification
Regulatory Affairs Certification (Canada)
La Régie de l’assurance maladie 
Reference Drug Program
Research Ethics Board
Prescription
Supplemental Abbreviated New Drug Submission
Special Access Program
Special Access Request
Standards Council of Canada
Self-Inspection	
Submission Information Policy Devision
Site Licence
Supplemental New Drug Submission
Standard Operating Procedure
Site Reference Files
Standard Sanitation Operating Procedures
Therapeutic Products Directorate
United States Pharmacopeia
Veterinary Drugs Directorate
Veterinary Natural Health Product
World Health Organization

Abbreviated New Drug Submissions
Access to Information Requests or Responses
Adverse Drug Reporting
Adverse Reaction Reporting
Analytical method validation
Annual Product Reviews
Assessments of Change Control
Audits
Batch Document Review
Biologics
Calibration Programs
Carrier qualification
Category IV Submissions
Cleaning Validation
Clinical Trial Applications
Cold Chain
Computer Validation
Controlled Drugs
Controlled Substances
Cooler Mapping
Cooler Validation
Cosmetic Notifications
Cosmetic Registrations
Cosmetic Regulations
Dealer’s License/Permit
Devices
Disinfectants
Documentation Review
Domestic Substances List
Drug Identification Number
Drug Submissions
DSL Registration
Due Diligence Assessments
Equipment Qualification
Equipment Validation
Establishment Licences (Licenses)
Establishment Licensing
Facility Qualification
Food and Drug Regulations
Food and Drugs Act
Formulary Listing Submissions
Freeze thaw Studies
Freezer Mapping
Freezer Validation
GAP Analysis
GCP Audits
GCP Training
GLP Audits

GLP Training
GMP Audits
GMP Training
Good Manufacturing Practices
Guide 0069
HAACP Audits
HACCP Training
Health Canada
Herbal Medicines
Herbal Remedies
HPFBI Inspection Preparedness
ICH Guidelines
Import Permits
Importer of Record
INCI Labelling Review
Incubator mapping
Incubator validation
Investigational New Drug Submission
Labelling Review
Labelling Standard 
Legal Agent
Submissions
Laboratory Audits
Mandatory Problem Reports
Manufacturing Site Audits
Mapping
Market Access
Medical Device Regulations
Narcotic Dealer’s licence
Narcotic Dealer’s license
Narcotics
Natural Health Product Regulations
Natural Health Products
Natural Product Number
NC Submission
New Drug Submissions
NHP Submissions
Notifiable Change Submissions
Packaging qualification
Packaging Validation
Pest Control Products
PMRA Submissions
Precursor A Submissions
Precursor B Submissions
Private Payer Plans
Process Validation
Product Assessment
Product Licence Applications

Product License Applications
Product Registrations
Product Releases
QC Release of Products
Quality Assurance
Quality Assurance Reports
Quality Control
Reduced Testing Programs
Regulation Interpretation
Regulatory Affairs
Reimbursement
Review of Stability Protocols or Data
Review of Validation Protocols or  Data
Risk Management
Rx to OTC
Sanitation Programs
Self-Inspections
Shipping Container Mapping
Shipping Container Validation
Shipping Route Qualification
Shipping Route Verification
Simulated HPFBI Inspections
Site Licences
Site Licencing
Site Licenses
Site Licensing
Site Reference Files
Six Sigma
Specification Reviews
Stability Data Summaries
Stability Programs
Standard Operating Procedures
Statistical Analysis
Statistical Process Control
Storage area mapping
Submission Preparation
Supplemental Abbreviated New Drug Submissions
Supplemental New Drug Submission
Temperature Mapping
Test Methods
Third Party Audits
Training Programs
Transportation vehicle mapping
Transportation vehicle 
Validation Programs
Warehouse Audits
Warehouse Mapping
WHO Export Certificates
… and many more

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