Bulletin MMC
Gcp 2013
Patient's rights and gcp compliant informed consent #cph may 2012
the tanzania food, drugs and cosmetics act, 2003
Investigator Responsibilities in Clinical Research Melissa Adde Director, Clinical Trials Office, INCTR .
1 International Clinical Trials: Current Issues in Clinical Trial Regulation and Future Reforms: EU, US, and Beyond: a European perspective International.
Zoe Whale / Lynette Lane GCP Facilitators, NISCHR CRC Good Clinical Practice in Research Clinical Trial Regulations.
Investigational Device Exemptions 21 CFR Part 812 A Review for OCRA US RAC Study Group September 2005 Ginger Clasby, MS Promedica International [email protected].
2013 HERDC - Research Income Return Information for Research Income Collection Co-ordinators Presented by: Tania Carrubba Research Management Accountant.
SAMSI Career Panel Kevin Anstrom May 24, 2005. Educational Background n Cornell University – studied applied statistics with focus on biology and agriculture.
1 FDA’s BIMO Inspection Program and IRB Inspections VA IRB Chairs Meeting August 2012 Janet Donnelly RAC, CIP Office of Good Clinical Practice Office of.
Online Proceedings
