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Site language : English - Français
Ref : 29031
Event :Compliance with the New ICH GCP Revision 2 Addendum

Date :Monday April 01st, 2019

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


Further information

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 directorfor M.Sc.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407

Further information

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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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Compliance with the New ICH GCP Revision 2 Addendum Medicine - Bio-Technologies - Toxicology - Public Health
education training, online training, medical conference, education & training
Everyone, QA Professionals Regulatory Affairs Pharmacovigilance
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For more information on Compliance with the New ICH GCP Revision 2 Addendum, plsase contactr Compliance4All

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