Compliance with the New ICH GCP Revision 2 Addendum
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Website https://www.compliance4all.com/control/w_product/~product_id=502387LIVE?channel=ourglocal_Apr_2019_S |
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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
Overview: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 OversightUnderstand requirements for CROs, quality systemsExplore risk based approaches for clinical trialsConsider changes for the TMFBest practice for Clinical QMSWho Will Benefit:Global Clinical Safety and Pharmacovigilance OfficersCompliance StaffClinical Quality AuditorsQuality Assurance PersonnelDocument managementSpeaker 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 $150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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