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Product Registration

Product evaluation mechanism


The necessary requirements are as follows:

An official letter addressed to the Director of product standardization and evaluation in the Department of Logistics and Contracts indicating your desire to evaluate the items, provided with a simple explanation of the uses of the item, in addition to any useful information in 5 to 7 lines and prepare a detailed table of the product including:

- Stock number (if the item is used by the health affairs of Ministry of National Guard).


- The factory name.


- Scientific description of the item.


- Trade Name.


- Catalog number.


- Country of Origin.


- Product validity.


- Price.


  • Attach all documents related to the product, such as, brochures, CDs, etc...
  • Attach approval of Saudi Food and Drug Administration (SFDA), and US Food and Drug Administration (FDA) or European Accreditation.
  • Attach product safety data-sheet.
  • Attach technical data-sheet.
  • Samples: Samples shall be submitted for each item, and to be in its original form and quantity shall be sufficient.

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Last Modified

5/22/2023 11:16 AM