Yes

The manufacturer should fill out the risk assessment form

Everyone can report: users, health practitioners, manufacturers, authorized representatives, suppliers or distributors.

1. Import/export of medical radioactive materials facility.
2. Transport of medical radioactive materials facility.
3. Healthcare providers that use radioactive materials.
4. Production of medical radioactive materials facility.

All pesticides used in controlling public health pests.

Through the link below:
https://sfda.gov.sa/ar/saudi_standards_lists?keys=&standards_title_eng=&standards_number=&page=0

Technical regulations and standard specifications can be obtained through the standard web store:

https://mwasfah.sfda.gov.sa/Home

In order the name of the beneficiary appears, the medical facility must register in the electronic system, and  complete all requirements and take the final approval of the application, and It is possible to add radioactive material or manufacturer by sending an E mail to Radiological Health Exicutive Dept. : rh.md@sfda.gov.sa

The local manufactures, the overseas manufactures, Authorized Representative, Importers, Distributors and the health practitioner must report incidents and adverse events to SFDA upon becoming aware it happens