Wed, 07/12/2017 - 12:03
With ISO 13485:2016—“Medical devices—Quality management systems—Requirements for regulatory purposes” published and being implemented, many medical device customers are experiencing some uncertainty about the effect that one of the standard’s key…Claire McCluskie
Claire McCluskie has worked within Ideagen’s Life Sciences team for over three years. During that time she has built a deep understanding of the industry demands and requirements, particularly in the topics of validation and data integrity. Aligning her knowledge of the industry and Ideagen’s products and services to the business needs of the industry is a key objective of her role.