Training - Education & Training Programme (ETP) - History and previous meetings

Educational Training Programme (ETP) – Archived Meetings


1. List of previous training at Annual Meetings and location
2. List of other training courses that ISoP has run and location

ISoP Training course - Education

History and previous meetings

1. List of previous training at Annual Meetings and location

Pre/post conference courses:

ISoP 2014 (Tianjin)

Principle of meta-Analysis
Core and Emerging issues in ADR reporting and Pharmacovigilance including the potential role of Consumer reporting (A Train the Trainer Programme)
Communication in PV

ISoP 2013 (Pisa)

Risk management planning and activities: PAES and PASS
Adverse drug reactions: clinical approach and differential diagnosis as the basis of case report quality

ISoP 2012 (Cancun)

Basic Concepts in PV
Vaccines: Pharmacovigilance of Adverse Events Following Immunisation
New EU post-licensing legislation – EU and beyond

ISoP 2011 (Istanbul)

Basic Concepts in PV
Causality assessment
Good Pharmacovigilance Practice – Inspection and audits (1/2 day)
Crisis management – Expecting the worst (1/2 day)

ISoP 2010 (Accra)

Vaccine Safety
Clinical Trial Safety
Basic concepts in PV
Creating a Safety Culture

ISoP 2009 (Reims)

Basic concepts in Pharmacovigilance
Risk Management
Qualified Person for Pharmacovigilance
Communications challenges in patient safety: Partnerships, PILs and preventing Patient harm in cyber space

ISoP 2008 (Buenos Aires)

From fundamental basis to practice
Drug-related Risk Management

ISoP 2007 (Bournemouth)

Back to basics
How to write a safety Specification and Risk Management Plan?

ISoP 2006 (Liege)

Risk Managements Plans
Introduction to Pharmacovigilance

ISoP 2005 (Manila)

Basic knowledge in pharmacovigilance & pharmacoepidemiology for beginners
Basic communication skills in pharmacovigilance
Risk assessment and risk management
The clinical diagnosis and management of ADRs
Pharmacovigilance planning for the industry

ISoP 2004

(no conference courses)

ISoP 2003 (Marrakech)

Writing papers for peer-reviewed journals (in French)
Compliance in Pharmacovigilance

ISoP 2002 (Amsterdam)

How to determine and to describe in the SPC frequencies of adverse drug reactions?

ISoP 2001 (Tunis)

Standardised causality assessment with single case reports of adverse events

2. List of other training courses that ISoP has run and location

Full details about our mid-year training courses: click here

Zagreb

2014 – Proactive Pharmacovigilance and Risk Management in the Era of Personalised Medicine
ISoP training course, 3 and 4 April 2014
In collaboration with the Agency for Medicinal Products and Medical Devices of Croatia (HALMED)

TOPRA / ISoP Conference

2013 – Practical Application of Benefit-Risk Assessment
23 September 2013, Brussels, Belgium

Singapore

2013- Pharmacovigilance Across Borders in Asia
ISoP Asia Symposium, 19 and 21 March 2013
in collaboration with the WHO-West-Pacific Regional Office and WHO-Uppsala Monitoring Centre.

Berlin

2012- New EU Post-Licensing Legislation and Benefit-Risk Management
ISoP Training Course, 11 and 12 June 2012 and (in parallel)
2012 – Future Perspectives for EU Pharmacovigilance
ISoP Training Course, 11 and 12 June 2012

Minsk

2011- Reporting, Causality Assessment, Risk factors & Mechanisms of ADRs
ISoP Training Course, 26 and 27 May 2011 and (in parallel)
2011- Risk Management and Regulatory inspections
ISoP Training Course, 26 and 27 May 2011
in collaboration with the Centre for Examinations and Testing in Health Service of the Republic of Belarus

Belgrade

2010- Basic concepts in pharmacovigilance
ISoP Training Course, 27 and 28 May 2010 and (in parallel)
2010- Clinical Trial Safety
ISoP Training Course, 27 and 28 May 2010
in collaboration with ALIMS (Medicines and Medical Devices Agency of Serbia) and the Faculty of Pharmacy, Belgrade.

Verona

2009- Basic concepts in pharmacovigilance
ISoP Training Course, 26 and 27 March 2009 and (in parallel)
2009- Keeping the lights green – your risk management roadmap
ISoP Training Course, 26 and 27 March 2009 and
2009 – Ecopharmacovigilance workshop

Bangkok

2008- Basic concepts in pharmacovigilance
ISoP Training Course, 17 and 18 March 2008 and (in parallel)
2008- Pharmacogenetics and drug safety
ISoP Training Course, 17 and 18 March 2008

Budapest

2007- Basic concepts in pharmacovigilance
ISoP Training Course, 22 and 23 March 2007 and (in parallel)
2007- Immunopharmacology and drug safety
ISoP Training Course, 22 and 23 March 2007

Sevilla

2006- Science and Regulation. Is this compatible?
Assessment and Management of Drug liver toxicity and copying with Audits and Inspections

ISoP Training Course, 2 and 3 February 2006, Sevilla, Spain

Barcelona

2005- New Challenges in Clinical Safety, Pharmacovigilance and Vaccine Vigilance
ISoP Training Course, 10 and 11 February 2005

Berlin

2004- Decision Making in Pharmacovigilance – Managing Risk
(Aspects and Criteria of Industry and Regulators)

ISoP Training Course, 29 and 30 January 2004

Paris

2003- Spontaneous ADR Reports vs. Pharmacoepidemiological Studies in Pharmacovigilance – Conflicts and Synergism
ISoP Training Course, 16 and 17 January 2003

Paris

2002- Standardised Causality Assessment
ISoP Training Course, 11 January 2002

Bordeaux

2000 – Assessing the individual case report
26 June 2000 – Bordeaux

(last updated 19 Nov 2014)