Refine by
Locations
- USA
- Alabama
- Alaska
- Arizona
- Arkansas
- California
- Colorado
- Connecticut
- Delaware
- District Of Columbia
- Florida
- Georgia (Us)
- Hawaii
- Idaho
- Illinois
- Indiana
- Iowa
- Kansas
- Kentucky
- Louisiana
- Maine
- Maryland
- Massachusetts
- Michigan
- Minnesota
- Mississippi
- Missouri
- Montana
- Nebraska
- Nevada
- New Hampshire
- New Jersey
- New Mexico
- New York
- North Carolina
- North Dakota
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Vermont
- Virginia
- Washington
- West Virginia
- Wisconsin
- Wyoming
Medical Device Standards Services In Usa
5 services found
by:in2being, LLC based inSaline, MICHIGAN (USA)
Medical devices are powerful and essential tools in the healthcare industry. Because they come in direct contact with patients and can have an effect on them, ensuring they meet safety standards is a critical part of the development and manufacturing ...
Manufactured by:Nanosonics, Inc. based inSydney, AUSTRALIA
Appropriate storage is required to prevent recontamination of reprocessed medical devices. Standard storage conditions such as being clean, dry, away from extreme heat and UV light should be ...
Manufactured by:Syncro Medical based inLanghorne, PENNSYLVANIA (USA)
In many cases, the Requirements phase is the most difficult stage of new product development. Progress is stymied as companies struggle to define the requirements for an innovative new product. MIT’s Sloane Management Review refers to the “fuzzy front end” as the “area of greatest weakness in new product ...
by:BSI Consulting based inHerndon, VIRGINIA (USA)
BSI Compliance Navigator is the smart, simple way to manage your regulatory information for Medical Device and In Vitro Diagnostic products with EU, UK and US requirements – helping you to get to market faster and maximize your ...
by:Product Safety Consulting, Inc. based inBensenville, ILLINOIS (USA)
Careful attention to product compliance and certification are an integral part of the process of developing and marketing medical devices. Certifiers, regulators,and standards-writing bodies such as Underwriters Laboratories (UL), the Canadian Standards Authority, the IEC and the FDA have been working hard to keep up with the ...
