The various regulations all over the world have established requirements for applications to market new medical devices. Also included is the necessity to demonstrate the product safety and to evaluate the biocompatibility.

SA-FORD addresses the following issues…

• the need to examine the potential toxicity of medical device materials,
  
• to appreciate the unique problems associated with medical device safety evaluation,
  
• to present novel testing methodologies.
  

SA-FORD conducts the biological evaluation of medical devices by strictly adhering to ISO 10993 guidelines