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Compliance for Risk Based Approaches for (Clinical Trials 2018)

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Website http://www.compliance4all.com/control/w_product/~product_id=502073LIVE?channel=ourglocal_Sep_2018_SE | Edit Freely

Category Clinical Managers, Project Managers, Lead Clinical Research Associates

Deadline: September 10, 2018 | Date: September 12, 2018

Venue/Country: Online, U.S.A

Updated: 2018-07-04 15:25:14 (GMT+9)

Call For Papers - CFP

Overview:

FDA and EMA have communicated their expectations for trial 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:

This essential webseminar will explain the importance of using risk 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:

Have explained key risk based process/tools and techniques

Review a risk based approach to protocol design

Understand risk based approach to monitoring/data handling

Hear best practice of these new risk requirements

Who Will Benefit:

Clinical Development Managers and Personnel

Clinical Research Archiving and Document Management Personnel

Quality Assurance Managers and Auditors

Consultants

Regulatory Affairs Specialists

Pharmacovigilance /Drug Safety

Study Site Personnel

Speaker Profile:

Dr. Laura Brown , PhD, MBA, Diploma Clinical Sciences, is an 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:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.