international pharmaceutical compliance congress
international pharmaceutical compliance congress
international pharmaceutical compliance congress
international pharmaceutical compliance congress
international pharmaceutical compliance congress
international pharmaceutical compliance congress



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International Pharma Congress: IFPMA Code Workshop and Ethical Promotion Roundtable
Sunday, May 4, 2014


In an effort to cover organizational expenses IFPMA is charging a small fee of €145 per participant. Registration deadline: May 1, 2014 (since workshop capacity is limited, we encourage early registration to secure a spot).
Click here to register.
THE IFPMA CODE WORKSHOP: HANDS-ON COMPLIANCE TRAINING
WORKSHOP FEE
  • In an effort to cover organizational expenses IFPMA is charging a small fee of €145 per participant.
WORKSHOP AIMS
    The workshop has been designed to provide "business case" exposure to individuals responsible:
  • for day-to-day commissioning and creation of promotional material and to those writing and approving copy and artwork
  • for determining promotional methods including professional representation, hospitality to doctors and the use of audio-visual and related communications technology in the organization of international educational events The workshop will be based on the global IFPMA Code of Practices (2012) which forms the basis for national codes of practice within the Middle-East and Africa region and world-wide.
WHO SHOULD ATTEND?
  • Representatives from biopharmaceutical companies and national pharmaceutical trade associations
  • Compliance professionals
  • Personnel responsible for the development and certification of promotional materials
  • Sales and Marketing representatives
  • General Managers
  • In-house counsel and other related staff
CAPACITY
  • Workshop capacity is limited and registration confirmation will be on a first-come, first-served basis. Therefore, please make sure to register early in order to secure a place in the workshop.
REGISTRATION CERTIFICATE

A certificate of participation will be awarded upon the completion of the workshop. If you have any questions please contact the IFPMA Secretariat at ccn-registration@ifpma.org.

WORKSHOP AGENDA
8:30 a.m.

Welcome and Introductions

Tamara Music
Manager, Influenza Vaccines and Code Compliance, IFPMA, Geneva, Switzerland

    Speaker Bio

    Tamara Music joined the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) in 2007 and is a Manager leading the Influenza Vaccines Supply (IVS) International Task Force as well as the transparency and ethics initiatives which include the IFPMA Code of Practice and the Code Compliance Network (CCN). Previously, Tamara has also worked on global health policy topics related to healthcare systems and market access. Tamara received her B.A. in Political Science from University of California, Berkeley, her Masters in International Affairs from the Graduate Institute in Geneva, and Certificate of Advanced Studies (CAS) in Pharmaceutical Economics and Policy from University of Lausanne, School of Business (HEC).
8:40 a.m.

Setting the Scene -- The Future of Marketing, Compliance and Ethics: The Expanding Role of the Compliance Officer

Abdul Luheshi, MBA
Vice President, Health Care Compliance, Johnson & Johnson; Former Co-chair, Asia Pacific Pharma Congress, London, UK

    Speaker Bio

    Dr. Luheshi has been with Johnson & Johnson for 14 years, of which 5 years as Head of Compliance for LifeScan EMEA and 4 years leading the health care compliance team for Janssen Pharmaceuticals in Asia. Currently based between the UK and China overseeing program enhancement initiatives for Johnson & Johnson

    Experience includes: implementation of international compliance program (developed, developing and emerging markets); anti-bribery/anti-corruption / FCPA investigations; risk assessments across multi-jurisdictional organizations; responses to external regulatory enforcement actions and management of third party relationships with respect to risk mitigation.

    Originally an organic chemist, post-MBA has held posts in operations management and finance across the chemical, agrichemical and healthcare industries.
9:15 a.m.

The Spirit of the Code: Our Values and Principles

Roeland Van Aelst
Vice President, Health Care Compliance, Medical Devices and Diagnostics, EMEA-C, HCC&P, Johnson & Johnson; Board Member and Co-chair, Strategic Committee, International Society of Healthcare, Ethics and Compliance Professionals (ethics); Chairman, EUCOMED Compliance Network, Brussels, Belgium

    Speaker Bio

    Roeland joined Johnson & Johnson in 1987 as a Medical Representative for Janssen Pharmaceutica. He held various positions of increasing responsibility in both sales and marketing and joined the WWOHCC&P in May 2005 for the EMEA region with extension to Asia, Latin-America and Canada in 2008. In 2010 Roeland became responsible for EMEA & Canada cross sector. Regional Vice President - HCCO MD&D EMEA & Canada is his current position since October 2012. Currently he also fulfills the Chairman role of the EUCOMED compliance network and is a member of the board and a founding member of ETHICS.
9:45 a.m.

Defining Promotion: Supporting Patient Programs

Heather Simmonds
Director, Prescription Medicines Code of Practice Authority, London, UK

    Speaker Bio

    Heather Simmonds is the Director of the Prescription Medicines Code of Practice Authority (PMCPA). Heather chairs the Code of Practice Panel, which considers complaints submitted under the Code in the first instance, and is responsible for the overall running of the organisation. Heather also works with IFPMA and EFPIA in relation to their codes of practice.

    Heather has a degree in pharmacology and joined the ABPI in 1984. Heather has been working full time on the Code of Practice since 1989 and has been Director of the Authority since 1997.
10:30 a.m. Coffee Break
10:45 a.m.

Part 1 -- Interactions with HCPs: Meetings, Sponsorship and Fees for Service

Cécile Gousset, AVP
Compliance Risk Assessment, Education and Monitoring, Global Compliance, Sanofi, Paris, France
11:30 a.m.

Part 2 -- Interactions with HCPs: Gifts and Other Items

Dominique Laymand
Vice President, Compliance and Ethics EMEA, (Europe, Middle-East, Africa, Russia and Turkey), Bristol-Myers Squibb; President, International Society of Healthcare, Ethics and Compliance Professionals (ethics), Paris, France

    Speaker Bio

    Dominique Laymand is Vice-President Compliance & Ethics EMEA (Europe, Middle East, Turkey, Russia and Africa). In this role, Dominique is responsible for maintaining, monitoring and controlling the Compliance & Ethics program based on an integrated approach of risks in terms of prevention, detection and control. She works closely with the EMEA Business leadership teams to establish policy oversight and governance via an efficient and effective Compliance & Ethics Program. She has a particular focus on Business Practices and is a member of operational committees as well as the Bristol-Myers Squibb Corporate Compliance Council and Anti-Bribery Committee.

    Dominique has a broad experience at Bristol-Myers Squibb, having started with the company in 1983 as Legal Counsel.

    Dominique is an active member of various Pharmaceutical Industry Associations and committees, proactively addressing Trust, Reputation and Compliance matters. She is the President of ETHICS Association; President of the Compliance Committee at the European Federation of Pharmaceutical Industries and Associations (EFPIA) and at the Compliance Committee at the LEEM (French Pharmaceutical Industry Association).
12:15 p.m. Networking Lunch
1:15 p.m. Business simulation Compliance Game: Fees for Service

ISMS
3:15 p.m. Coffee Break
3:30 p.m.

Congress Organization: How to Interact and Practical Cases

Jose F. Zamarriego Izquierdo
Director Unidad de Supervision Deontologica, FARMAINDUSTRIA, Madrid, Spain

    Speaker Bio

    Jose Zamarriego has been the Director of the Code of Practice Surveillance Unit of the National Association of the Pharmaceutical Industry in Spain (Farmaindustria) since the establishment of this Compliance Control Body in 2004. Together with his team he oversees implementation and compliance with the self-regulation system of the pharmaceutical industry, adapting and anticipating to the growing demands of a society in constant evolution. At a European level, Jose is Chair of the EFPIA (European Federation of Pharmaceutical Industries and Associations) Code Compliance Committee and Vice-Chair of the Compliance Committee. He is also Chairman of the IFPMA (International Federation of Pharmaceutical Manufacturers & Associations) Code Complaint Procedure Adjudication Group. He has actively participated in several modifications of national, European and worldwide codes of practice for the pharmaceutical industry. Jose completed his PhD. on Economics & Business Studies in the Universidad Complutense de Madrid, expanding his education with an MBA on Business Administration by the University of Wales and a General Management Program by the IESE Business School. Before joining the innovative pharma association, he was General Secretary and General Director of the Spanish Generic Pharmaceutical Manufacturers Association (AESEG). Jose also has a background as an educator in the Universidad Europea de Madrid (UEM), where he was Dean of the Faculty of Economics and Business Administration and Executive Director of the UEM General Foundation.
    Presentation Material (Acrobat)
4:15 p.m.

Thermometer Game: How Hot is this issue?

Jan Oliver Huber
Secretary General, PHARMIG (Association of the Austrian Pharmaceutical Industry); Member, IFPMA Code Compliance Network, Vienna, Austria
Heather Simmonds
Director, Prescription Medicines Code of Practice Authority, London, UK

    Speaker Bio

    Heather Simmonds is the Director of the Prescription Medicines Code of Practice Authority (PMCPA). Heather chairs the Code of Practice Panel, which considers complaints submitted under the Code in the first instance, and is responsible for the overall running of the organisation. Heather also works with IFPMA and EFPIA in relation to their codes of practice.

    Heather has a degree in pharmacology and joined the ABPI in 1984. Heather has been working full time on the Code of Practice since 1989 and has been Director of the Authority since 1997.
5:30 p.m.

Interactive Discussion and Q&A

Rifat Bozacioglu
Deputy Compliance Officer, Compliance Business Partner, MEA Pharma Compliance, GlaxoSmithKline, Istanbul, Turkey
6:00 p.m. Adjournment




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