CSA Z314:23, Canadian medical device reprocessing in all health care settings (CSA Z314:23), addresses the safe, effective, and reliable reprocessing of reusable medical devices and supplies.
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The standard CSA Z662 was created to help provide guidance on the safe design, construction, and maintenance of oil and gas pipeline systems.
Medical device manufacturers must consider safety from many perspectives. Learn about the specific regulatory requirements for the North American market.
Unique circumstances could make it challenging, impractical, or even impossible for manufacturers to undergo the typical certification process yet demonstrate commitment to product compliance with applicable standards. This webinar will walk you through the available programs designed to solve these challenges, how to identify the need for these programs, and how to avoid common mistakes.
Safety analysis can be complicated and time exhaustive. Achieving compliance with electrical safety standards for electronics and embedded software for safety monitoring and critical safety controls may not be enough.
Learn why functional safety should be considered early in the design process.
Understand the latest updates to UL 1973 for stationary storage systems covering cells, battery modules, battery pack/rack, and the battery management system.
Comprehending these updates is vital for manufacturers as they plan milestones and time-to-market for their products.
The new Mexican Conformity Assessment Procedure for Telecommunication Products extends the scope of certification, increases alignment with global tre
The new Mexican Conformity Assessment Procedure for Telecommunication Products introduces four new certification schemes and a flexible homologation process.
Regulatory landscape, construction, and testing requirements for EV batteries covered under the scope of UL 2580
Wireless devices have become a key part of our everyday life. They often access our personal information and communication networks.