Netzealous LLC DBA - Compliance4All, Online
2019-04-01
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 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
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: compliance4all14@gmail.com
|