Canada's MDEL (Medical Device Establishment License) is a license for medical device business premises, not a license for specific medical device products. The annual audit is usually conducted on a regular basis each year to ensure that the medical device premises are still in compliance with Health Canada regulations and standards.
The exact timing of the annual review may vary depending on the location and circumstances of the equipment, so you will need to check Health Canada's regulations for details. Typically, MDEL holders are required to submit an annual review within a specific period of time each year so that the Ministry of Health can review and renew their license.
In order to ensure that the annual review is carried out in a timely manner, MDEL holders should pay close attention to the notices and requirements of the Ministry of Health and submit the required annual review documents within the stipulated timeframe. Failure to conduct the annual review on time may lead to the invalidation of the MDEL, which will affect the legality of the operation of medical devices and equipment.
In conclusion, the annual review time of MDEL is usually carried out regularly every year, and the specific time will vary depending on the situation, MDEL holders should pay close attention to the notice of the Ministry of Health and submit the annual review documents on time to maintain their legitimacy.