Compliance with the New ICH GCP Revision 2 Addendum

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Category ICH GCP R2 Addendum, Pharmacovigilance Guidelines, Compliance Trainings, ich gcp guidelines, ich gcp guidelines pdf, ich gcp e6 revision 2 essential documents, Online Clinical Courses

Deadline: March 31, 2019 | Date: April 01, 2019

Venue/Country: Online, U.S.A

Updated: 2019-02-18 15:27:02 (GMT+9)

Call For Papers - CFP

This will enable you to meet the new international GCP standard to ensure regulatory compliance and the acceptance of clinical trial data by the regulatory authorities internationally.

Why should you Attend:

With the new ICH GCP E6 Revision 2 Addendum now finalised the changes should have been implemented for organisations running clinical trials.

Areas Covered in the Session:

Review the new requirements for Sponsor and Investigator Oversight

Understand requirements for CROs, quality systems

Explore risk based approaches for clinical trials

Consider changes for the TMF

Best practice for Clinical QMS

Who Will Benefit:

Global Clinical Safety and Pharmacovigilance Officers

Compliance Staff

Clinical Quality Auditors

Quality Assurance Personnel

Document management

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.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: compliance4all14gmail.com