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1 2nd annua event Limited specia offer save up to $755. The earier you book the more you save! Prices, packages and booking form on back page Hear from Apri 2010, The Westin Grand, Washington DC, United States Dr Martin Huber Vice President Goba Pharmacovigiance, Deputy Chief Medica Officer Schering-Pough Safety assured Dr Jose Vega Vice President Goba Safety Amgen Addressing the key chaenges for safety professionas wordwide Drug safety strategy update incuding a goba reguatory round up, pre and post marketing safety strategy, risk management, data management, inspections, drug safety infrastructure considerations and much more pages 4 & 5 >> Dr Phiippe Van der Auwera Goba Head of Safety Risk Management, EU-QPPV F Hoffmann-La Roche Meet the experts shaping the drug safety environment incuding goba reguators, industry-eading experts and thought eaders page 3 >> Don t just sit there! Interactive & fexibe agenda, unique networking opportunities, pane discussions, Q&A, workshops and mutipe streams page 6 >> Dr Vaerie Perentesis Executive Director, Operations & Externa Affairs, Goba Pharmacovigiance and Epidemioogy Bristo-Myers Squibb Pre & post conference workshops: 20 Apri 2010 Designing and impementing a computerized pharmacovigiance database system 23 Apri 2010 Effective risk management for a sound safety strategy A detais page 6 >> Speaker ine up more detais page 3 Fu conference programme pages 4 5 Pre and post workshops page 6 A booking offers & options back page Book eary and save up to $755! Pus the FDA! Sponsors: Produced by: More highights Page 3 >> Fu programme Pages 4-5 >> BOOK NOW! onine emai phone +44 (0) fax +44 (0)

2 book eary and save Word Drug Safety Congress Americas day God Pass Save $755 if you register before 30 January 2010 And another $100 if you book and pay onine See Page 8 Exceent content, deivery and interaction Director Goba Pharmacovigiance, Bayer Heathcare The speakers were good, with exceent presentations and usefu information Director of Drug Safety Management, Shanghai Roche How prepared are you for the current unprecedented drug safety chaenges? The annua Word Drug Safety Congress Americas 2010 is back, foowing an impressive aunch in 2009, and it promises to be even bigger and better than before. Safety is a critica eement for the entire ifecyce of a drug. The right safety strategy promises to aid R&D efficiency; strengthen risk management functions; ease the pressure of meeting reguatory demands; address post marketing safety requirements and improve safety communication & patient trust. This congress provides the perfect patform for you to examine how you can make and fufi the right safety strategy; a fundamenta decision to ensuring the ong term success of a drug. What you asked from us: Huge speaker pane of top industry speakers High eve speaker seniority Reguatory experts Strategy ed content Pentifu pane discussions In-depth case studies Extensive networking opportunities Soutions-based discussions Rea experiences from the industry s best Safety in specia popuations adds another significant chaenge to the drug deveopment process. Using the exampe of pediatrics, how have Roche estabished a successfu strategy to meet regiona reguations and ensure risk minimization? Preparation is we underway for the exponentia rise in adverse events expected as the use of H1N1 vaccine rises. MedImmune discuss how their risk management strategy has been deveoped and what the specific drug safety considerations for vaccine products are. The industry is under enormous strain in the face of increasing reguatory pressure and pubic focus on safety. How can we move to a more proactive system and strive to overcome the chaenges faced daiy? Amgen s Dr Jose Vega brings his unique experience to bear on these critica issues. Maintaining pace with the continuousy evoving reguatory environment is a time and resource consuming process. The FDA, Japan s PMDA and goba industry representatives expore the most recent reguatory updates and how to adapt to the changing requirements. The key topics to be addressed; Goba drug safety environment Chaenges in today s drug safety industry Internationa reguatory round up Safety data management Post-marketing safety strategy Cinica safety strategy Risk management and minimization strategies Pharmacovigiance inspections processes The compete safety ifecyce of a drug from eary deveopment through to post authorization The evoving reationship between socia media and drug safety Pharmacoepidemioogy Drug safety in specia popuations Training and infrastructure requirements for drug safety operations Exceent The best PV programme this year Senior Director, Safety & Risk Management, Pfizer Industry sectors: pharmaceutica, biotech and CROs Pharmacovigiance Eectronic submissions Drug Safety Who s attending? Risk Management and Surveiance Cinica Safety Epidemioogy Quaified Person Reguatory Affairs 2 BOOK NOW! onine emai phone +44 (0) fax +44 (0)

3 book eary and save 8 REASONS Why you shoud attend Word Drug Safety Congress Americas 2010: 1. Fuy packed agenda Over 30 sessions, mutipe streams and workshop options for you to taior the congress to meet your own information and networking needs 2. Top notch speaker pane Incuding Amgen, Asteas, Baxter, Bayer, BMS, Genzyme, Medimmune, Novartis, Otsuka, Pfizer, Roche, Schering-Pough, Wyeth and many more 3. Quaity content Confronting the topics you want and need to hear 4. Over 80% new speakers New insights and fresh industry strategies 5. Wide goba reach We have industry and reguatory representatives from Europe, America and Asia to give a much needed view of internationa safety operations 6. A proven track record Foowing an exceptiona aunch in 2009, this event promises to be bigger and better than ever 7. More case studies Hear the good, the bad and the ugy experiences from the industry s best and utiize them to strengthen your own drug safety strategy 8. Extensive networking Pan who to meet prior to the conference with the contact system, take part in speed networking to meet more peope in ess time and continue those conversations into the compimentary evening drinks reception The Heath Network difference Heath Network events create exciting paces to... interact and grow knowedge meet and make contacts become inspired and reenergised use your brain A-ist industry experts Risk management throughout a product s ifecyce: integrated safety business Mariette Boerstoe-Streefand, Chief Safety Officer, Vice President Goba Drug Safety Forest Research Institute, Forest Laboratories Leveraging technoogy to faciitate an efficient SAE reporting process Adrian Hsing, Senior Director Cinica Data Management, Giead Sciences, Inc. Driving pharmacovigiance and epidemioogy forward: innovation, harmonization and gobaization Andrew Bate, Director, Quantitative Epidemioogist, Safety & Risk management, Pfizer Specia considerations of safety in oncoogy patients: edery patients Wei Dong, Goba Head of Epidemioogy for Oncoogy, Genentech Impementation and monitoring of a risk management pan Robin Geer, Director of Risk Management Goba Pharmacovigiance, Baxter Heathcare Corporation Optimizing physicians and heathcare professionas in goba pharmacovigiance Leann Fiedstad, Goba Head Compiance, PDS, Hoffmann-La Roche Managing earning in the pharmacovigiance and compiance environment Nancy Grey, Director, Safety and Risk Management, Pfizer Chaenges in deveoping an efficient, effective AE monitoring system; one sma to midsize company's experience Eeanor Sega, Vice President, Medica Safety Officer, Acteion Pharmaceuticas The roe of observationa epidemioogy studies in drug safety evauation: oncoogy therapeutic area Jerzy Tyczynski, Director Goba Surveiance & Pharmacoepidemioogy Goba Medica Services GPRMS, Abbott Laboratories Your event contact is Karen Wiiams +44 (0) heathnetworkcommunications.com Thank you for a nice meeting... I met many new peope and earned a ot from different perspectives Senior Medica Assessor, Medica Products Agency, Sweden We presented taks which had the audience interested and engaged Head Pharmacovigiance Information Management, Wordwide Deveopment, Pfizer Exceptiona speaker facuty: hear from over 30 of the industry s best BOOK NOW! onine emai phone +44 (0) fax +44 (0)

4 book eary and save Word Drug Safety Congress Americas 2010 Day One Wednesday 21 Apri Registration & coffee 9.00 Opening remarks from the chair 9.10 Proactive drug safety management: successfuy meeting the growing goba expectations Continuous assessment, proactive management and transparent communication of drug risks Addressing increasing reguatory and pubic focus on drug safety Enhanced centra roe of safety scientists in cinica drug deveopment Optimizing risk management and risk mitigation Dr José Vega, Vice President Goba Safety, Amgen 9.40 Drug safety considerations for vaccine products How has the risk management strategy been deveoped for the expected exponentia rise in AE reports foowing the increased H1N1 jab use? Sean Darcy, Director Product Safety, MedImmune foowed by morning refreshments GLOBAL REGULATORY ROUND UP Drug safety reguatory deveopments in the USA An update on FDAAA, e-reporting, REMS and the Sentine Initiative George Rochester, Acting Director, Division of Biometrics VII, Quantitative Safety and Pharmacoepidemioogy Group, FDA Drug safety reguatory deveopments in Europe A focus on CIOMS, AE and periodic reporting, RMP, Voume 9a, Eurdravigiance, DSURs and the roe of the QPPV Dominique Deattre, Senior Director Pharmacovigiance and Risk Management Europe, Sanofi Pasteur MSD Drug safety reguatory deveopments in Japan Reguations for cinica trias, drug safety reporting and EPPV Dr Junko Sato, Director for Risk Management, Office of Safety II, Pharmaceuticas and Medica Devices Agency (PMDA), Japan Drug safety in Asia Regiona differences for drug safety in Asia incuding Korea, Taiwan, China and Japan Inspection readiness in Asia with consideration of Voume 9a Chaenges for DSUR preparation Shinya Yamauchi, Operating Officer Pharmacovigiance Department, Otsuka Pharmaceuticas Further discussion on the goba drug safety andscape In addition to the morning s speakers: Susan Boynton, Executive Director, Therapeutic Area Head, Goba Reguatory Affairs & Safety, Amgen Mathias Hukkehoven, Senior Vice President and Head of Portfoio Stewardship Board, Novartis Lourdes Frau, Vice-President and Head, Goba Patient Safety, Vertex Pharmaceuticas Lunch STREAM 1: RISK MANAGEMENT STRATEGY 1.50 Opening remarks from the chair Dr Sabine Richter, Vice President Safety & Risk Management, PRA Internationa 2.00 Risk management throughout a product s ifecyce: integrated safety business Dr Mariette Boerstoe-Streefand, Chief Safety Officer, Vice President Goba Drug Safety, Forest Research Institute, Forest Laboratories 2.30 Eements to ensure safe use: a practica guide to FDA REMS components Mark Neson Tyrre, Director, Risk Management, PRA Internationa 3.00 Impementation and monitoring of a risk management pan Robin Geer, Director of Risk Management Goba Pharmacovigiance, Baxter Heathcare Corporation 3.30 Afternoon refreshments SAFETY DATA MANAGEMENT 4.00 Data mining to risk management pan: the safety signa sojourn at Genzyme Meg Richards, Director, Goba Patient Safety & Risk Management, Genzyme 4.30 Leveraging technoogy to faciitate an efficient SAE reporting process Adrian Hsing, Senior Director Cinica Data Management, Giead Sciences 5.00 Scope and context for product safety assessment panning Potentia ways to address drug safety from FDA initiatives Quantitative Safety Anaysis Pan (QSAP) Observationa Medica Outcomes Partnership New idea for conducting arger, simper, randomized treatment trias George Rochester, Acting Director, Division of Biometrics VII, Quantitative Safety and Pharmacoepidemioogy Group, FDA OR 1.50 Opening remarks from the chair 2.00 Post-marketing signa detection: the roe of medica evauation Anthony Lassiter, Senior Medica Director, Product Safety and Pharmacovigiance, Asteas Pharma 2.30 Improving post marketing safety NOW: a case study and pan for the future Michae Ibara, Head of Pharmacovigiance Information Management, Pfizer 3.00 Optimizing physicians and heathcare professionas in goba pharmacovigiance Leann Fiedstad, Goba Head Compiance, PDS, Hoffmann- La Roche 3.30 Afternoon refreshments 4.00 Post marketing safety risk management strategies incuding deveoping and impementing REMS United Biosource Corporation 4.30 The use of epidemioogy in drug safety strategy Biy Hoden, Head, Risk Benefit Management and Pharmacoepidemioogy Pharmacovigiance and Pubic Heath, Vertex Pharmaceuticas 5.30 STREAM 2: POST MARKETING SAFETY STRATEGY Drinks reception: join your peers and reax after a busy conference day. To sponsor the drinks reception contact Roope Ghosh on +44 (0) Register before 30 January and save up to $755! Fax the registration form to +44 (0) BOOK NOW! onine emai phone +44 (0) fax +44 (0)

5 book eary and save Day Two Thursday 22 Apri Registration & coffee 9.00 Opening remarks from the Chair Dr Wytske Kingma, Senior Vice President and Goba Head Patient Safety and Risk Management, Genzyme 9.10 New era of safety risk panning Changing reguatory andscape Initiatives undertaken by heath authorities Pharma infrastructure required to meet the chaenge The future of safety risk management Dr Vaerie Perentesis, Executive Director, Operations & Externa Affairs, Goba Pharmacovigiance and Epidemioogy, Bristo-Myers Squibb 9.40 Web based AE reporting; is it the future? Pharma's current use of socia media How can socia media be incorporated into a drug s safety strategy and what are the chaenges? John Mack, Editor & Pubisher, Pharma Marketing News Pharmacovigiance inspections; preparation, impementation and essons earnt Deveopment of a quaity management system approach within pharmacovigiance Pre-inspection readiness and ogistics Recommendations for activities during the inspection Dr Martin Huber, Vice President Goba Pharmacovigiance, Deputy Chief Medica Officer, Schering-Pough Morning refreshments DRUG SAFETY INFRASTRUCTURE REQUIREMENTS Chaenges in deveoping an efficient, effective AE monitoring system: one sma to midsize company's experience Defining your company's needs Productive strategies to enhance AE coection: data entry, review, anaysis and reporting Tips from experience at a company that grew from sma to midsize in 10 years Eeanor Sega, Vice President, Medica Safety Officer, Acteion Pharmaceuticas 1.30 Driving pharmacovigiance and epidemioogy forward: innovation, harmonization and gobaization Provide an overview of recent progress in signa detection in EHRs and caims data CIOMS VIII working party: harmonization in signa detection FNIH s OMOP pubic private partnership between FDA and industry Recent goba initiatives and the future impact on safety operations Andrew Bate, Director, Quantitative Epidemioogist, Safety & Risk management, Pfizer 2.00 Benefit-risk: essons earned from systematic impementation during phase III deveopment Various quaitative and quantitative approaches to benefit / risk Advantages of a more expicit and discipined critica anaysis of the data Quantitative investigations of decision-making on benefit / risk attributes by patients, prescribers and care-givers Dr Phiippe Van der Auwera, Goba Head of Safety Risk Management, EU-QPPV, F Hoffmann-La Roche DRUG SAFETY FOR SPECIAL POPULATIONS 2.30 Specific safety & pharmacovigiance in chidren: one more chaenge in drug deveopment Specific pediatric requirements in EU and US EMEA guideine on pediatric pharmacovigiance Precinica and cinica pediatric safety considerations PIP (Pediatric Investigation Pan) and pediatric risk minimization Kaus Rose, Head Pediatrics, Medica Science, Roche 3.00 Specia considerations of safety in oncoogy patients: edery patients Understanding disease epidemioogy among cancer patients pertaining to their advanced age, high co-morbidities and compex heathcare systems Opportunities and chaenges of this specia popuation Wei Dong, Goba Head of Epidemioogy for Oncoogy, Genentech 3.30 Cose of conference and afternoon refreshments Managing earning in the pharmacovigiance and compiance environment Buiding technica and soft skis curricua Training's roe in reguatory inspections elearning's impact in compiance training Deveoping customized training through roe based scenario's Nancy Grey, Director, Safety and Risk Management, Pfizer The roe of observationa epidemioogy studies in drug safety evauation: oncoogy therapeutic area How epidemioogy contributes to both pre and postmarketing safety evauation Sources of data for observationa studies in oncoogy Using popuation-based cancer registries data in drug safety evauation: what needs to be done to effectivey utiize this type of data? Jerzy Tyczynski, Director Goba Surveiance & Pharmacoepidemioogy Goba Medica Services GPRMS, Abbott Laboratories Lunch Hear from and meet your industry peers Group bookings Save up to 25% if you bring your team BOOK NOW! onine emai phone +44 (0) fax +44 (0)

6 book eary and save Word Drug Safety Congress Americas 2010 Get the most from your conference Pre-conference workshop Post-conference workshop Tuesday 20 Apri 2010 Friday 23 Apri 2010 Designing and impementing a computerized pharmacovigiance database system Pre & post conference workshops Effective risk management for a sound safety strategy Fun, high speed breaks for making new contacts and exchanging detais. Arrange meetings onine before you arrive, access event resources such as papers and presentations after you ve eft. Meet and tak about the business issues on your brain. Situated in the styish West End district of the nation s capita, The Westin Grand, Washington DC enjoys an unbeatabe ocation. Whether you are visiting for business or eisure, you are moments away from Embassy Row, the White House, and Georgetown. Workshops: a reaxed environment for you to network with your peers and focus more directy on topica issues. 4 day God pass. Save $755 before 30 January 2010! See page 8. This workshop wi provide an overview of the current goba reguatory environment for adverse event reporting, the chaenges of buiding an efficient adverse event database system for processing the signas and how it can affect your overa safety strategies. This is an interactive workshop session, featuring penty of presenter, attendee interface and discussion. Overview 8.30 Registration & coffee 9.00 Review of adverse event reporting history and reguations for investigationa and icensed products History and rationae Drugs, bioogics and devices Impact of CIOMS and ICH Morning refreshments US and internationa reguations USA reguations series, 600 series, 800 series EMEA reguations Cinica Tria Directive, Vo. 9a ROW reguations QA impact Lunch 1.15 Design, impementation and vaidation of computerized adverse event database systems Budgets, money and manpower User requirements System requirements 3.00 Afternoon refreshments 3.15 Vaidation Instaation quaification Operationa quaification Production quaification Go ive Your workshop eader Mike Boh, Founder, Drug Safety Net LLC Mike is a consutant to the pharmaceutica industry with over 12 years of pharmacovigiance and risk management experience. He has worked with arge and sma pharmaceutica organizations in resoving pharmacovigiance issues. Mike served as a member of the PhARMA reguatory, safety and nomencature subcommittees for the bioogic industry. He currenty is a member of the Drug Information Association Cinica Safety and Pharmacovigiance Specia Interest Community. In that roe he serves on the internationa core committee and is communication coordinator. This one day interactive workshop wi provide an indepth review of risk management and the roe it pays throughout the entire ife cyce of a drug. The day wi address both the oca and goba reguatory environment and considerations for risk management strategies as we as providing interesting exampes or risk management and minimization activities. Overview Registration and coffee Background and overview of recent RM activities Current approaches to risk assessment Assessing the need for a RMP Routine (most products) vs. risk minimization / REMS (seected products) Morning refreshments Goba reguatory environment ICH E2E and Eudra Vo. 9A contents of the safety specification and the pharmacovigiance pan FDA guidances (risk assessment and minimization) Genera considerations for deveoping risk management and risk mitigation pans Lunch 1.15 Exampes of risk management and risk minimization activities Additiona information gathering e.g. registries, post-approva safety studies, sentine sites Heightened surveiance Enhanced communication patients, prescribers 2.15 Afternoon refreshments 2.30 Further exampes Enhanced prescriber education Access contro Monitoring and assessment of effectiveness 3.15 Group discussion, Q&A, and wrap-up Your workshop eader Dr Sidney Kahn, Founder & President, Pharmacovigiance & Risk Management Inc. Sidney is the Founder and President of Pharmacovigiance & Risk Management, Inc, (www. pvrm.com) providing independent expert advice on a aspects of pharmacovigiance and risk assessment and mitigation to pharmaceutica companies and industry support organizations wordwide. 6 BOOK NOW! onine emai phone +44 (0) fax +44 (0)

7 book eary and save Becoming a sponsor or exhibitor The Word Drug Safety Congress Americas is now in its 2nd year! The inaugura event in Apri of 2009 was an unprecedented success with a record number of attendees and strong sponsor presence. After the exceent feedback from both sponsors and deegates aike, we expect the conference to grow in Position yoursef where peope come to ook for advice, guidance and support to the key chaenges they face. As a CRO or technoogy provider with soutions to offer, this conference represents an exceptiona opportunity to deveop new business reationships. Questions to determine your invovement Do you offer services and soutions that support the chaenges faced in drug safety? Coud you benefit from introductions to and time with decision makers in drug safety? Meet and do business with industry decision makers. Are you activey ooking for new eads and cients to work with from the drug safety community? If your answer is yes to these questions you shoud be participating in this event, and by doing so you wi increase your chances of being seected as a partner. Sponsorship opportunities can be taiored to your specific objectives and marketing requirements, et us know what you want to achieve and we wi deveop a promotiona soution with you. To sponsor or exhibit contact Roope Ghosh on +44 (0) or emai heathnetworkcommunications.com Best organised event I have participated in during the ast 12 months Director of Observationa Studies, Covance Good presentations, good mix of attendees (pharma, agencies/ academics, vendors), professionay organized VP, Safety & Risk Management, PRA Internationa Sponsors Media partners PRA's Safety & Risk Management team has over 100 experts who can assist your organization in impementing and conducting, safety & risk management duties throughout your product's ifecyce. Offering services such as: ICSR processing, iterature search, product ca center, risk evauation, aggregate report generation, and risk management activities. UBC, United BioSource Corporation, is a goba pharmaceutica services organisation that combines deep scientific knowedge with broad execution expertise across the entire ifecyce continuum. Our focus is on generating rea-word data to support the deveopment and commerciaisation of medica products for emerging and estabished ife science companies. UBC s areas of expertise incude risk management consuting and impementation of post-approva studies, incuding product registries and arge streamined studies. Register before 30 January and save up to $755! Fax the registration form to +44 (0) BOOK NOW! onine emai phone +44 (0) fax +44 (0)

8 book eary and save Word Drug Safety Congress Americas 2010 Safety assured Apri 2010, The Westin Grand, Washington DC, United States Use our onine cacuator at You can use our onine cacuator to taior your ticket and buy mutipe tickets. The cacuator automaticay seects the most favourabe discount for you. If you book and pay onine you aso save a further $100. Register now Package Before 30 Jan 2010 Before 13 Mar 2010 Before 3 Apr 2010 After 3 Apr 2010 How many Cacuate your ticket God pass a 4 days $3400 $3775 $3965 $ Apri main days pus pre conference workshop March main days pus post conference workshop March day conference March 2010 *Registrations without credit/debit card payments are subject to a $100 booking fee. Your voucher code Your detais Deegate name... Job tite...organization... Address... Post code...country... Te...Fax... Emai... Authorizing manager...authorizing manager signature... Payment detais $2595 $2595 $1790 $2885 $2885 $1990 (you need to quote this for teephone and onine bookings) A tickets incude refreshments, unch and fu conference documentation. The fee does not incude hote accommodation. Payment is due in 7 days. By signing and returning this form you are accepting our terms and conditions. If you reserve your ticket but pay by bank transfer or cheque payment must be received in 7 days Bank transfer Cheque Visa Mastercard Amex Card number Expiry date: / / Card hoder's name... Card hoder's signature... Security code:... Bank Transfers: Account name: Heath Network Communications, Sort code: , Bank Account Number: , Bank Name & Address: Barcays Bank, Capham High Street, London SW4 4UF, Swift Address: BARCGB22, IBANGB68 BARC Reference: pease quote and the deegate s name $3030 $3030 $2090 $3175 $3175 $2190 How do you want to pay? Tota Credit / Debit card $ 0 Cheque / Bank transfer $ 100 How to book your ticket Onine You can use our onine cacuator to taior your ticket and buy mutipe tickets. The cacuator automaticay seects the most favourabe discount for you. If you book and pay onine you aso save a further $100. Offine You can use our onine cacuator to taior your ticket and then print a pdf of your order and fax to +44 (0) or compete this form and fax to +44 (0) or ca +44 (0) and we take your booking over the phone. Group bookings Why not send your team and save more. Send 3 deegates and save 15% Send 6 deegates and save 25% Ca +44(0) or go onine and register Privacy poicy Heath Network Communications (or its agents) may contact you by mai, phone or emai about products and services offered by Heath Network Communications and its group companies, which Heath Network Communications beieves may be of interest to you, or about reevant products and services offered by reputabe third parties. Heath Network Communications may aso discose your contact detais to such third parties to enabe them to contact you directy. Certain entities to which Heath Network Communications discoses your contact detais are ocated in territories overseas which have fewer ega safeguards to protect persona data. By returning this form to us, you agree to our processing of your persona information in this way. Pease tick the appropriate box if you do not wish to receive such information from: Heath Network Communications; or reputabe third parties. Canceation poicy 1. Shoud you be unabe to attend, a substitute deegate is wecome at no extra charge 2. Heath Network Communications does not provide refunds for canceations. Invoiced sums are payabe in fu, except in cases where Heath Network Communications has been abe to mitigate oss 3. Heath Network Communications wi make avaiabe course documentation to a deegate who is unabe to attend and who has paid 4. Heath Network Communications reserves the right to ater the programme without notice incuding the substitution, ateration or canceation of speakers and / or topics and / or the ateration of the dates of the event 5. Heath Network Communications is not responsibe for any oss or damage as a resut of a substitution, aternation, postponement or canceation of an event If you reserve your ticket but pay by invoice or bank transfer payment must be received in 7 days 8 BOOK NOW! onine emai phone +44 (0) fax +44 (0)

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