Q-27 C Reporting of Adverse Events of Medical Devices
This SOP defines the procedures to follow when reporting Adverse Events of Medical Devices in order to be compliant with the provisions of the Medicines Act as well as the relevant SAHPRA Guidelines.
- SOP branded with your company logo
- SOP supplied in PDF format
Hevan van der Westhuizen ex Chief Medical Control Inspector for the MCC.
Once your purchase has been processed an Alec Cameron representative will contact you for your company details and company logo, once supplied we will send you your copy within 48hrs.