On June 16, 2016, the Food and Drug Administration (FDA) released a draft guidance entitled Factors to Consider Regarding Benefit-Risk in Medical Device Product Availability, Compliance, and Enforcement Decisions[2]. The...more
Large or small, every life science or medical technology company will eventually have to deal with a products liability claim or event. A lack of adequate planning for such an occurrence can result in damage to the brand,...more
6/11/2015
/ Best Management Practices ,
Life Sciences ,
Manufacturers ,
Medical Devices ,
Product Defects ,
Product Labels ,
Product Packaging ,
Product Recalls ,
Product Safety Labels ,
Safety Precautions ,
Safety Training ,
Technology
As technology continues to evolve, so do the ways in which patients and healthcare providers obtain information pertaining to medical products regulated by the Food and Drug Administration (FDA). Thomas Abrams, Director of...more
7/23/2014
/ Draft Guidance ,
Food and Drug Administration (FDA) ,
Health Care Providers ,
Internet ,
Manufacturers ,
Marketing ,
Medical Devices ,
Pharmaceutical Industry ,
Prescription Drugs ,
Social Networks ,
Twitter