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Itted to this office must be complete and include all fees, documents/ attachments. A preliminary review for correct fees will occur upon submission. No further review will occur if the fees are incorrect. Any incomplete application will not be accepted for processing and will be returned in its entirety. The processing time is contingent upon the complexity of the application. GENERAL INSTRUCTIONS 1. Indicate the type of license being requested in the space provided. 2. Type or print clearly a.

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SUMMARY. Health Canada is the federal body that regulates the drug approval process under the Food and Drugs Act (FDA) and its regulations (FDR), its related policies and guidance.

The Pharmaceutical Drugs Directorate (formerly the Therapeutic Products Directorate (TPD)) is Canada's regulator of prescription pharmaceutical drugs for human use.

Determining your device classification in Canada There are four device classifications — Class I, II, III and IV — using a set of 16 rules found in Canadian Medical Devices Regulations. In vitro diagnostic (IVD) devices are also classified as Class I through IV using a set of nine rules.

The Bureau of Consumer Health Product Modernization is responsible for modernizing the regulation of self-care products, including natural health products, cosmetics and over-the-counter drugs in Canada.

Contacts for Natural Health Products For general enquiries relating to licensing natural health products, please contact the Natural and Non-prescription Health Products Directorate (NNHPD), by email at nnhpd-dpsnso@hc-sc.gc.ca.

This Bureau is responsible for reviewing applications for new and amended medical device licences for: digital health devices (for example, diagnostic imaging devices, therapeutic lasers, software devices)

Health Canada plays an active role in ensuring that you have access to safe and effective drugs and health products. The Department strives to maintain a balance between the potential health benefits and risks posed by all drugs and health products. Our highest priority in determining the balance is public safety.

Over the counter, non prescription drugs are regulated by Health Canada to address product safety and to reduce health risks to consumers. When a product label contains a DIN, consumers can be confident that it meets the requirements for safety, quality and effectiveness set out by Health Canada.

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© Copyright 1997-2025
airSlate Legal Forms, Inc.
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Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232