2011 Public Presentations

1-2 Feb 2011 : Informa : London
Conference Title : Product Information Management
Chair & Speaker
Presentation Title : Overview of the Status of Product Information Management (PIM)

2 Feb 2011 : Informa : London
Conference Title : Lifecycle Management of the eCTD
Speaker
Presentation Title : Overview of the Status of Product Information Management (PIM)

9 Feb 2011 : European Center of Pharmaceutical Medicine : Basel
Course Title : Module 5: Global Registration and Approval Process
Speaker
Presentation Title : Electronic Submissions

17 Feb 2011 : Aveiro University : Lisbon
Course Title : Training Programme in Pharmaceutical Medicine – Regulatory Affairs
Speaker
Presentation Title : Common Technical Document and Electronic Submissions

3 March 2011 : IQPC : London
Conference Title : Pharmaceutical Regulatory Information Management
Speaker
Presentation : Harmonisation of eCTD and Nees Validation Criteria

7-9 March 2011 : Informa : Frankfurt
Conference Title : Regulatory Information Management
Workshop Faculty, Chair & Speaker
Workshop Title : How to Set-up and Implement a Regulatory Information Management Project
Presentation Title : Upcoming standards for identification of medicinal products: Potential impacts

28-30 March 2011 : Drug Information Association : Geneva
Conference Title : 23rd Annual Euromeeting
Programme Committee, Theme Co-Chair, Session Chair & Panel Member
Theme Title : Knowledge Management and Telematics: Enhancing exchange between industry and regulators and improving support for their decision-making
Panel Discussion Title : Best Practice In Electronic Information Exchange For Regulatory Submissions

5 April 2011 : Drug Information Association : London
Conference Title : EMA Information Day: 2nd Information Day on the New Individual Case Safety Report (ICSR) International Standard and ICH E2B/M2
Speaker
Presentation Title : Latest status of the process of the international standards development

17 May 2011 : Liquent : Barcelona
Conference Title : Horizons 2011
Speaker
Presentation Title : Upcoming standards for Identification on Medicinal Products : Potential impacts and timelines

9 June 2011 : Liquent/NextDocs : Huntingdon, UK
Conference Title : Integrated Regulatory Compliance Management : From Document to Submission
Speaker
Presentation Title : Information Management Processes Integration for Life Sciences – from an Industry Expert’s Perspective

13 September 2011 : Liquent : Webinar
Speaker
Presentation Title : Complying with the New Pharmacovigilance Legislation

21 September 2011 : Aris Global : London
Conference Title : EVMPD – Off to New Horizons
Speaker
Presentation Title : How to Comply with the EMA’s New Pharmacovigilance Legislation

19-20 October 2011 : Informa : London
Conference Title : Pharmaceutical Labelling
Speaker
Presentation Title : Assessing how industry will address the gap left by PIM’s cessation

1 November 2011 : FX Conferences : Webinar
Speaker
Presentation Title
: Complying with EMA’s New Mandatory Requirements for Medicinal Product Information (EVMPD)

17 November 2011 : CSC Life Sciences : Webinar
Speaker
Presentation Title : Preparing for EMA’s EVMPD Mandate

30 November  – 2 December 2011 : Drug Information Association : Zurich
Conference Title : 12th Conference on European Electronic Document Management
Speaker
Presentation Title : On-Going Progress of the IRISS Forums
Presentation Title : Preparing for EMA’s EVMPD Mandate

6 December 2011: Appel Consulting : London
Conference Title : Pharmacovigilance Global Summit
Speaker
Presentation Title : The impact of EMAs announcement to make submission of EVMPD data mandatory