Date: | September 12, 2018 - 10:00am - 11:00am |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | 161 Mission Falls Lane, Suite 216,, Fremont, CA, 94539, United States |
Website for Event: | http://www.compliance4all.com/control/w_product/~product_id=502073LIVE?channel=s... |
Topic: | Health Coach and Health Coaching |
Description: | Overview: oversight/ monitoring, monitoring systems, and investigative site oversight. These are described in the FDA Guidance Oversight of Clinical Investigations: A Risk- Based Approach to Monitoring and the EMA Reflection Paper on risk-based quality management in clinical trials both of which will be reviewed in this web seminar. Why should you Attend: management techniques in clinical research to comply with the latest focus on GCP inspection in this area. It will show you how risk management can improve the quality of your clinical trials and demonstrate the importance of using risk analysis and risk management techniques in clinical trials. Areas Covered in the Session: Who Will Benefit: Speaker Profile: independent QA and training consultant in the pharmaceutical industry. She is a managing director with LB Training and Development Ltd., course director for the M.Sc. in Clinical Research, School of Pharmacy at the University of Cardiff, and course director for M.Sc. Regulatory Affairs, TOPRA. Event Fee: One Dial-in One Attendee Price: US$150.00 Contact Detail: |
Contact Name: | Event Manager |
Contact Email: | support@compliance4All.com |
Contact Phone: | 8004479407 |