Pharmacovigilance

• Pharmacovigilance and Risk Management Strategies 2012
  Emne: Pharmacovigilance, Post Marketing, Risk Management, EU regulation, International regulation, Clinical trials, Risk Management, EU regulation, International regulation
  Udbyder: DIA
  Sted: Arlington, VA, USA
  Dato: 23-25 January 2012
  
• EMA Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing Training Course
  Emne: Pharmacovigilance, Clinical trials, Safety data, Post Marketing, Patient safety, Safety data
  Udbyder: DIA
  Sted: London, England
  Dato: 13-17 February 2012
  
• Training course on Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
  Emne: Pharmacovigilance, Clinical trials, Safety data, Post Marketing, Safety data, Patient safety
  Udbyder: DIA
  Sted: London, England
  Dato: 13-17 February 2012
  
• Extended EudraVigilance Medicinal Product Dictionary training course
  Emne: Pharmacovigilance, Post Marketing, EU regulation
  Udbyder: DIA
  Sted: London, England
  Dato: 14-15 February 2012
  
• Extended EudraVigilance Medicinal Product Dictionary training course
  Emne: Pharmacovigilance, Post Marketing, EU regulation, ICH
  Udbyder: DIA
  Sted: London, England
  Dato: 20-21 March 2012
  
• The New Individual Case Safety Report (ICSR) International Standard and ICH E2B/M2 Information Day (3rd)
  Emne: Pharmacovigilance, Post Marketing, EU regulation, ICH, Adverse Events, Compliance
  Udbyder: DIA
  Sted: London, England
  Dato: 4 May 2012
  
• Clinical Evaluation of Drug Products
  Emne: Pharmacovigilance, Clinical trials, QA, Compliance
  Udbyder: KU, FARMA
  Sted: Copenhagen, Denmark
  Dato: 21-25 May 2012
  

Courses from other providers

• ARCHIVED WEBINAR: Evaluating IRBs: Finding an IRB that is Compliant, Provides High Quality and Customer Service
  Emne: Pharmacovigilance, Clinical trials, Compliance
  Udbyder: DIA
  Sted: Internet
  Dato: Available April 14, 2011 through April 13, 2012
  
• Monitoring Safety in Clinical Trials and Drug Development
  Emne: Pharmacovigilance, Clinical trials, Audit / inspection, QA, QP, Risk Management, Safety data
  Udbyder: DSRU
  Sted: London, England
  Dato: 22-23 February 2012
  
• Adverse Events: Managing and Reporting for Medical Devices
  Emne:
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 23-24 February
  
• Practical Pharmacovigilance Auditing
  Emne: Pharmacovigilance, Clinical trials, Audit / inspection, Post Marketing, Audit / inspection
  Udbyder: BARQA
  Sted: Cambridge, England
  Dato: 28-29 February 2012
  
• Drug Safety and Pharmacovigilance
  Emne: Pharmacovigilance, Clinical trials, Safety data, Medical aspects, Drug interactions, Risk Management
  Udbyder: Barnett International
  Sted: San Fransisco, CA, USA
  Dato: 27-28 March 2012
  
• Pharmacovigilance in Europe
  Emne: Pharmacovigilance, Clinical trials, EU regulation, Compliance, QA, ICH
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 24-25 April 2012
  
• Adverse Events: Managing and Reporting for Pharmaceuticals
  Emne: Pharmacovigilance, Clinical trials, Adverse Events, International regulation, Post Marketing, Adverse Events, International regulation, Safety data, MedDRA, Coding
  Udbyder: Barnett International
  Sted: Boston, MA, USA
  Dato: 7-8 June 2012
  
• Pharmacovigilance Audit
  Emne: Pharmacovigilance, Clinical trials, Audit / inspection, International regulation, Risk Management
  Udbyder: Barnett International
  Sted: Philadelphia, PA, USA
  Dato: 20 June 2012
  
• Adverse Events: Managing and Reporting for Medical Devices
  Emne: Pharmacovigilance, Clinical trials, Adverse Events, Compliance, International regulation, Devices, Adverse Events, US regulation, MedDRA
  Udbyder: Barnett International
  Sted: San Fransisco, CA, USA
  Dato: 25-26 June 2012
  
• A Practical Guide to Pharmacovigilance and Drug Safety
  Emne: Pharmacovigilance, Clinical trials, Safety data, QA, Practice, ICH, Compliance, Risk Management, QP, Post Marketing, EU regulation, International regulation, Risk Management, QP, Compliance, PSUR, Safety data
  Udbyder: IIR PTI
  Sted: Internet
  Dato: Ongoing
  
• An Introduction to Pharmacovigilance (PV)
  Emne: Pharmacovigilance, Clinical trials, Practice, Adverse Events, Safety data, Risk Management, Post Marketing, Patient safety, PSUR, Risk Management, Safety data, Adverse Events, Practice
  Udbyder: Zenosis
  Sted: Internet
  Dato: Ongoing