REFERENCES


Safety and Quality Assurance icons 

 

 

ISO 9000 Quality Management, the International Organization for Standardization (Click on icon for more information)

 

ISO 13485 Quality Management Systems for Medical Devices.(Click on icon for more information)

 

The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives for European Community.

(Click on icon for more information)

 

The Food and Drug Administration (FDA) is an agency within the U.S. Department of Health and Human Services. (Click on icon for more information)

 

GMP (Good Manufacturing Practice) provides for systems that assure proper design, monitoring, and control of manufacturing processes and facilities.  Adherence to the cGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations.

(click on icon for more information)

New products

No new products at this time

Newsletter