This article discusses the legal and practical issues around the duty to warn and instruct and where to place safety information on the product and/or in the manual.
The pandemic has brought many changes in the way we do business. For equipment manufacturers, that may equate to big picture shifts related to your supply chain, vendors, and production. Here, let’s explore key considerations to keep in mind for your product safety strategy, warnings, and instructions.
This article explains the development process of a proficiency testing programme that is suitable for electrical and mechanical safety tests. The process for testing the homogeneity and stability of specimens is also discussed.
The way you market your product can turn an otherwise safely designed product into an unsafe product that causes injury and creates liability for the manufacturer and product seller.
This article discusses additional requirements that designers and safety professionals may want to consider beyond the base standard for their product based on the environment and user exposure.
This article provides an overview of lifecycle issues for interoperable medical products that are not sufficiently addressed in existing medical device standards and identifies lifecycle concepts from other domains that may be adapted for interoperable medical systems.
Product markings and labels provide information about the product, installation, and use. The markings and labels can also provide warnings to avoid hazardous energy transfer to a body part. The product safety aspects of markings for identification, ratings, functions, connections, and warnings are described.