Private label applications
(PDF version, 255 KB, 7 pages)
On this page
- 1 - Regional Administrative
- 5 - Labelling and Promotional Material
- 5.02 - Product/Package Labels
- 5.03 - Package Insert/Instructions for Use
- 5.04 - e-labelling
- 5.05 - Physician Labelling
- 5.06 - Patient Labelling
- 5.07 - Technical/Operators Manual
- 5.08 - Patient File Stickers/Cards and Implant Registration Cards
- 5.09 - Product Brochures
- 5.10 - Other Labelling and Promotional Material
1 - Regional Administrative
Folder name: 1-REG ADMIN
Note: No files or content should be included at this level. Only sub-folders of this folder should contain documents.
1.01 - Cover Letter
Folder name: 1.01-Cover Letter
Health Canada guidance
Generally cover letters are not required. In special circumstances where content is considered important but does not belong elsewhere in the application, it can be included in a cover letter.
Classification
Private label applications:
- Conditionally required - If information needs to be included that does not appear somewhere else in the application
1.04 - Application Form/Administrative Information
Folder name: 1.04-Application Form-Administrative Info
Health Canada guidance
A copy of the relevant Health Canada Application and Fee Forms for the application - refer to www.canada.ca for the most up to date forms.
Classification
Private label applications:
- Required
1.09 - Pre-Submission Correspondence and Previous Regulator Interactions
Folder name: 1.09-Pre-Submission Correspondence-Previous Regulator Interactions
Health Canada guidance
During the product lifecycle, pre-submission correspondence, including teleconferences or meetings, may be held between the regulator and the applicant. Further, the specific subject device may have been subject to previous regulatory submissions to the regulator or correspondence to confirm device risk class. A summary of these interactions and copies of any meeting minutes or emails are to be provided. The contents should be limited to the subject device as similar devices are addressed in other areas of the submission.
Note: The scope of this section is limited to the particular regulator to which the submission is being submitted (i.e. Health Canada does not need pre-submission information relating to interactions with the USFDA).
Classification
Private label applications:
- Conditionally required - If applicable
1.14 - Other Regional Administrative Information
Folder name: 1.14-Other Regional Administrative Info
Health Canada guidance
For Private Label applications (new and amendments), include the Letter of Authorization and Declaration of Compliance.
For all Fax-Backs (Minor Changes), include a copy of the front page of each affected licence.
Classification
Private label applications:
- Required
5 - Labelling and Promotional Material
Folder name: 5-LABELLING
Note: No files or content should be included at this level. Only sub-folders of this folder should contain documents.
5.02 - Product/Package Labels
Folder name: 5.02-Product-Package Labels
Health Canada guidance
Samples of the primary and secondary packaging labels but exclusive of labels for shipping.
Note:
- All labelling must be provided in English or French, both official languages are to be available upon request.
- Labelling for near-patient devices must also be provided in French and English.
Classification
Private label applications:
- Conditionally required - If applicable
5.03 - Package Insert/Instructions for Use
Folder name: 5.03-Package Insert-Instructions for Use
Health Canada guidance
Package Insert/Instructions for Use included in the package, when required or provide support for why this element is not applicable.
Note:
- All labelling must be provided in English or French, both official languages are to be available upon request.
- Labelling for near-patient devices must also be provided in French and English.
Classification
Private label applications:
- Conditionally required - If applicable
5.04 - e-labelling
Folder name: 5.04-e-labelling
Health Canada guidance
- For eligible medical devices and stand-alone software, the applicant needs to identify which form of e-labelling is being used in case of e-labelling (e.g. electronic storage system or built-in system, website).
- Provide details of risk management in relation to e-labelling. If this is part of the overall risk management, refer to it here.
- A description of the procedure and operations on providing IFU's when requested.
- Provide written information for user Information on webpage where IFU and further information can be found in relevant languages.
- Description on how the requirements detailed for the website have been met.
Classification
Private label applications:
- Optional
5.05 - Physician Labelling
Folder name: 5.05-Physician Labelling
Health Canada guidance
Labelling directed at the physician other than the package insert, such as the surgical manual.
Classification
Private label applications:
- Conditionally required - If applicable
5.06 - Patient Labelling
Folder name: 5.06-Patient Labelling
Health Canada guidance
Labelling directed at the patient other than the package insert, such as informational material written to be comprehended by the patient or lay caregiver.
Classification
Private label applications:
- Conditionally required - If applicable
5.07 - Technical/Operators Manual
Folder name: 5.07-Technical-Operator Manual
Health Canada guidance
Labelling directed the technical users and operators of medical devices focusing on the proper use and maintenance of the device.
Classification
Private label applications:
- Conditionally required - If applicable
5.08 - Patient File Stickers/Cards and Implant Registration Cards
Folder name: 5.08-Patient File Stickers-Cards-Implant Registration Cards
Health Canada guidance
- stickers/cards intended to be place in the patient's chart identifying the implant (e.g. serial #, lot#, make, model).
- If applicable, implant registration cards.
- The sponsor/applicant should explicitly address any existing regional regulatory guidance related to labelling the subject device.
Classification
Private label applications:
- Conditionally required - If applicable
5.09 - Product Brochures
Folder name: 5.09-Product Brochures
Health Canada guidance
- Draft product brochures available at the time of application.
- The sponsor/applicant should explicitly address any existing regional regulatory guidance related to labelling the subject device.
Classification
Private label applications:
- Conditionally required - If applicable
5.10 - Other Labelling and Promotional Material
Folder name: 5.10-Other Labelling-Promotional Material
Health Canada guidance
Heading for other information that may be important to the submission but that does not fit in any of the other headings of this chapter.
Classification
Private label applications:
- Conditionally required - If applicable
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