Quarterly Bulletin M alaysian M edic al Council 01-2008 KDN:UKP 100-3/3 Jld.2-(29) CONTENTS President’s Foreword Editorial Reflection Mediation Secretary’s Report Highlights…

1. GCP ICH Dr. Ghiath Alahmad 2. Goals and Objectives • To understand: ▫ The affect of Good Clinical Practices on institutions conducting Clinical Research • To discuss:…

1. GCP-COMPLIANTINFORMED CONSENT &OTHER PATIENT’S RIGHTS ATTY. ELIZABETH R. PULUMBARITUniversity of the Philippines Manila© February 2010; May 2011; May 2012 2. HOSPITAL’S…

1. THE TANZANIA FOOD, DRUGS AND COSMETICS ACT, 2003 ARRANGEMENT OF SECTIONSSectionTitle PART I PRELIMINARY PROVISIONS1. Short title and Commencement. 2. Application. 3. Interpretation.…

Slide 1Investigator Responsibilities in Clinical Research Melissa Adde Director, Clinical Trials Office, INCTR www.inctr.org Slide 2 Topics to be Discussed Overview of Clinical…

Slide 11 International Clinical Trials: Current Issues in Clinical Trial Regulation and Future Reforms: EU, US, and Beyond: a European perspective International Pharmaceutical…

Slide 1Zoe Whale / Lynette Lane GCP Facilitators, NISCHR CRC Good Clinical Practice in Research Clinical Trial Regulations Slide 2 At the end of this session, I hope you…

Slide 1Investigational Device Exemptions 21 CFR Part 812 A Review for OCRA US RAC Study Group September 2005 Ginger Clasby, MS Promedica International [email protected]…

Slide 12013 HERDC - Research Income Return Information for Research Income Collection Co-ordinators Presented by: Tania Carrubba Research Management Accountant Swinburne…

Slide 1SAMSI Career Panel Kevin Anstrom May 24, 2005 Slide 2 Educational Background n Cornell University – studied applied statistics with focus on biology and agriculture…