Pharmacovigilance
Courses from preferred partners
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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
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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
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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
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Extended EudraVigilance Medicinal Product Dictionary training course
Emne: Pharmacovigilance, Post Marketing, EU regulation
Udbyder: DIA
Sted: London, England
Dato: 14-15 February 2012
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Extended EudraVigilance Medicinal Product Dictionary training course
Emne: Pharmacovigilance, Post Marketing, EU regulation, ICH
Udbyder: DIA
Sted: London, England
Dato: 20-21 March 2012
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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
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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
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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
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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
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Adverse Events: Managing and Reporting for Medical Devices
Emne:
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 23-24 February
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Practical Pharmacovigilance Auditing
Emne: Pharmacovigilance, Clinical trials, Audit / inspection, Post Marketing, Audit / inspection
Udbyder: BARQA
Sted: Cambridge, England
Dato: 28-29 February 2012
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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
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Pharmacovigilance in Europe
Emne: Pharmacovigilance, Clinical trials, EU regulation, Compliance, QA, ICH
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 24-25 April 2012
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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
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Pharmacovigilance Audit
Emne: Pharmacovigilance, Clinical trials, Audit / inspection, International regulation, Risk Management
Udbyder: Barnett International
Sted: Philadelphia, PA, USA
Dato: 20 June 2012
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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
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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
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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