The ISO 14155: 2011 Clinical Investigation of Medical Devices for Human Subjects — Good Clinical Practice has been well received as a global standard for medical device GCP, including sponsor monitoring. This training course focuses on the application of the standard specific to the sponsor monitoring responsibilities & activities. This interactive session can be used as a foundation for training of sponsor study teams and monitors.
Attend this interactive live session and you will:
Who Should Attend:
This course will be of benefit to anyone that has a foundation in GCP, and is looking to apply that knowledge to medical device trials using the ISO 14155:2011 standard (global and domestic). Also, those involved in establishing standard operating procedures (SOPs) for investigational sites, auditing investigative sites, or training sites on global medical device clinical quality standards will find this course particularly useful. Finally, those who need to be conversant in the relationship between traditional GCP mandates for site monitoring vs. the ISO standard will find this course beneficial.
Sandra “SAM” Sather is an industry-leading consultant whose mission is to promote clinical quality systems for Sponsors/CROs and Investigators/Research Institutions. She has over 25 years of clinical experience, with a Bachelor of Science in Nursing and a Master of Science in Education with a Specialization in Training and Performance Improvement. SAM is the vice-president of Clinical Pathways, a consulting firm located in the Research Triangle Park area in North Carolina, USA. SAM is dual certified by the Association for Clinical Research Professionals (ACRP) for over 10 years (CCRA and CCRC) and a current member of the ACRP Academy Board of Trustees and Regulatory Affairs Committee (RAC). She is a frequent speaker for industry conferences and has authored dozens of courses for clinical research in various functional areas (e.g., monitoring, safety, HIPAA, and vendor management).