7th Annual Pharmaceutical Leadership Summit & Pharmaleaders Business Leadership Awards 2014
CQ5254 Pharmaceutical and Medical Device Labelling Summit
-
Upload
kiran-bains -
Category
Documents
-
view
151 -
download
0
Transcript of CQ5254 Pharmaceutical and Medical Device Labelling Summit
Optimise Your Labelling Strategies to Ensure Accurate Product Information and Successful Regulatory Compliance
27th – 29th October 2015Maritim proArte Hotel Berlin, Germany
Stream 1: Pharmaceutical Labelling and Company Core Data Sheets
Crucial regulatory feedback ensuring effective product information and practical case studies on successfully writing and managing company core data sheets
Stream 2: Labelling Compliance and UDI Implementation for Medical Devices and IVDs
Industry case studies and essential regulatory updates for the future of medical device and IVD labelling and practical implementation of the UDI system
Patricia Lefebvre Sanofi
Sponsors:
Exhibitors:
The Pharmaceutical and Medical Device Labelling Summit
Klaus Menges BfarM
Jackie Rae ElkinMedtronic
Doris I. Stenver PRAC
www.pmdlsummit.com
Steve GrahamDepartment of Health, UK
Igor KnezevicBayer Pharma AG,
Beth A. LageBaxter Healthcare
Guido ClaesJanssen
Géraldine Lissalde-BonnetGS1 Global Office
Peter BoegeNovo Nordisk
Laura LocatiAbbott Vascular
Pharmaceutical Labelling Medical Device and IVD Labelling08.00 Conference Registration
08.50 Opening Remarks from the Chairperson
09.00 Pharmaceutical Labelling: Considering the Patient Regulatory and Legal Considerations of Labelling
Dual Discussion: The Life of a Diabetes Patient: Improving the Readability of Pharmaceutical Drug Labels
Carien Van der Karel van der Waarde Graphic Design Researcher GLO, The Netherlands
Have Diabetes Patient The Netherlands
Dealing with the Medical Device DirectiveJoachim Wilke Director Regulatory Affairs & Policy Europe Medtronic, Germany
09.40 Translating Pharmacovigilance Requirements into Effective Patient Information - Assessing the Relationship Between PV and Labelling
Theo Raynor, Professor of Pharmacy Practice, School of Healthcare University of Leeds, UK
Industry Case Study – How to Control and Comply with Country Specific Labelling Requirements.
Bianca Maria Gravenhorst Greve Senior Regulatory Affairs Manager Coloplast, Denmark
10.20 Effective Labelling for Medical Communication, Patient Safety and Patient Adherence to the Treatment
Ruxandra Rogosca Drug Safety Unit Manager Berlin-Chemie A.Menarini, Romania
Industry Feedback from Stryker on Destination Labelling
Gil Lee Program Manager of Global Labeling Team Stryker Corporation, USA
11.00 Morning Coffee & Exhibition Viewing
11.30 Ensuring Accuracy in Labelling and Preventing Errors Willie Schnaubelt Managing Director Schlafender Hase GmbH, Germany
Panel Discussion: The Likelihood of Global Labelling HarmonisationThis morning’s speakers will make up the
PA NEL
facilitators of this session
12.10 Risk Management E-Labelling
Panel Discussion: Best Approaches and Strategies to Make Pharmaceutical Labelling More Patient FriendlyThis morning’s speakers will make up the
IN
TERA CTIVE
facilitators of this session
E-Labelling at a Global levelMaurizio Suppo Principal Consultant Qarad, Italy
12.50 Lunch & Exhibition Viewing
14.15 Closing the Gap Between Signal Detection and Implementation in the Label
Boris Jankowski Head of Solution Architecture Services Sciformix, USA
Spotlight Session
SPO TLIG HT
If you are interested in presenting on this topic please contact Linda Cole: Email [email protected], Tel: +44 (0)20 7017 6631
14.55 Hear from the Regulators The Experience Exchange
An Interview with BfArMKlaus Menges, Director, Federal Institute of Drugs and Medical Devices (BfArM), Germany
Labelling Experience Exchange:This interactive break-out session will allow attendees to discuss particular challenges encountered with the implementation of labelling strategies in an informal environment. Attendees will gather in different groups specific to their manufacturing products to guarantee an industry-specific and accurate learning experience through sharing of perspectives and challenges.
15.35 Afternoon Tea & Exhibition Viewing
16.05 Spotlight Session If you are interested in presenting on this topic please contact Linda Cole: Email [email protected], Tel: +44 (0)20 7017 6631
Implementing Radio Frequency Identification (RFID)
Industry Case Study - RFID and Labelling in Medical Devices. A Timid Foray into a New Regulated Industry
Erik Paul Manager Regulatory Affairs Olympus Winter & Ibe GmbH, Germany
16.45 Update From The Pharmacovigilance Risk Assessment Committee (PRAC)
Doris I. Stenver MPA Chief Medical Office Pharmacovigilance Risk Assessment Committee Delegate, Denmark
Risk Management
Labelling and Safety Risk Management According to ISO14971
Peter Boege, Design Controls and Risk Management Expert, NovoNordisk, Denmark
1725 Utilising the QR Code Dominique Westphal Scientific Expert, EU-Co-operation Paul-Ehrlich-Institute, Germany
17.25 Closing Remarks from the Chairperson
17.30 End of Day 1
18.05 Closing Remarks from the Chairperson & End of Day 1
Day Tuesday 27th October 2015 1
INTERA CTIVE
S
PO TLIG HT
Pharmaceutical Labelling Medical Device and IVD Labelling08.50 Opening Remarks from the Chairperson
09.00 E-labelling, Software and Databases The New NHS eProcurement Strategy and its Effect on Labelling
The Benefits Electronic Labelling Can Bring to Industry
Igor Knezevic Global Labeling Manager Bayer Pharma AG, Germany
The NHS eProcurement Strategy : Why All Goods and Services Supplied to the NHS Must Be Compliant with GS1 and PEPPOL Standards
Steve GrahameProcurement Lead, Commercial DirectorateDepartment of Health, UK
09.40 The Challenges and Opportunities in Transition from XEVMPD to ISO IDMP
Guido Claes Pharma R&D Drug Development Information Governance Janssen, Belgium
Content Management Systems (CMS)
How to Maximise Content Management Systems (CMS)Sebastian Gottel Executive Vice President SCHEMA Consulting GmbH, Germany
10.20 Linking Risk Management and LabellingPatricia Lefebvre Global Labeling - Global regulatory affairs Sanofi, France
Industry Feedback on Implementing Content Management Systems (CMS)
Katrin Thelen Technical Writer Bess, Germany
11.00 Morning Coffee & Exhibition Viewing
11.30 Quick-fire Technology Showcase: Demonstration of the Current Software on the Market to Assist Data ManagementIf you are interested in presenting on this topic please contact Linda Cole: Email [email protected], Tel: +44 (0)20 7017 6631
Taking a Closer Look at the Label
Dual Discussion: Industry and Patient Perspective : Improving the Readability of Medical Device Labels
Carien Van der Have Diabetes Patient, The Netherlands IN
TERA CTIVE
Jennifer Perkins Technical Communications Manager Thoratec, USA
12.10 Understanding and Dealing with Current Standards
Identifying and Marking Pharmaceutical Products Using GS1 Standards
Géraldine Lissalde-Bonnet Public Policy Senior Manager GS1 Global Office, Belgium
12.50 Lunch & Exhibition Viewing
14.15 Analysing the Importance of Tamper Proof Closures Stephen Wilkins Chief Executive Child-Safe Packaging Group, United Kingdom
Clarifying the Requirements for Symbols Used in Medical Device Labelling
Samantha Marshall Regulatory Affairs Manager EMEA Ansell Healthcare, UK
14.55 How to Manage Multiple Requests for Variation?Dorka Mihajlova Regulatory Specialists Alkaloid AD Skopje, Macedonia
Spotlight Session If you are interested in presenting on this topic
SPO TLIG HT
please contact Linda Cole: Email [email protected], Tel: +44 (0)20 7017 6631
15.35 Afternoon Tea & Speed Networking
16.05 Implementing Serialisation Guidance on Promotional Labelling
Serialisation: How? Why and When? Maarten Van Baelen Market Access Director, European Generic and Biosimilar Medicines Association (EGA)
Industry Feedback: Correctly Complying with Claims in Promotional Material
Elena Varini Intl Orthopedics Regulatory Manager Orthofix Srl, Italy
16.45 Interactive “Simulating the Campfire” SessionCome together in an informal environment to discuss the best approaches and strategies to prepare for serialisation
What are the Repercussions of Not Correctly Complying with Claims in Promotional Material
Shuna Mason Partner CMS Cameron McKenna LLP, UK
17.25 Closing Remarks from the Chairperson
17.30 End of Day 2
To register or for the latest information, please visit: www.pmdlsummit.com Tel: +44 (0)20 7017 7481 Email: [email protected]
Day Wednesday 28th October 20152
IN
TERA CTIVE
Company Core Data Sheets UDI Implementation08.50 Opening Remarks from the Chairperson
09.00 Implementing Company Core Data Sheets (CCDS) UDI in the US
How to Compile a Company Core Data Sheet (CCDS)Barbara Lachmann Labeling Consulting, Germany
Panel Discussion: Reflecting on the UDI Class 3 and 2 Deadlines in the US
Gil Lee
PAN EL
Program Manager of Global Labeling Team Stryker Corporation, USA
Jackie Rae Elkin Rob Bergman, Global Process . W. L. Gore & Associates, Inc. Standard Product Packaging & Labeling, USA Medtronic, USA
Sharing Experience on Core Company Data Sheet and Core Company Safety Information
Michel Mikhail Expert in Global Regulatory Affairs, Member of the US Pharmacopiea Committee of Experts, Member of the Federal Governmental Institue of Risk Assessment, Germany
Industry Case Studies
09.40 Industry Case Study: Best Practice and Strategies for Implementing UDI
Jenny Gough Process Development Manager/GS1 & UDI Specialist Operations-Value Chain Development and Efficiency Molnlycke Health Care, UK
10.20 How to Organise and Implement Company Core Data Sheets (CCDS)
Aaron Barzey Senior Executive - Global Regulatory Affairs Reckitt Benckiser, UK
Implementing the UDI System Using GS1 StandardsGéraldine Lissalde-Bonnet Public Policy Senior Manager GS1 Global Office, Belgium
11.00 Morning Coffee & Exhibition Viewing
11.30 Industry Experience of Company Core Data Sheets (CCDS)
Anna Paul Manager Global Regulatory Affairs Grunenthal, Germany
UDI Industry-Specific Experience Exchange: IN
TE R A C TIVE
This interactive break-out session will allow attendees to discuss particular challenges encountered with the implementation of UDI strategies in an informal environment. Attendees will gather in different groups specific to their manufacturing products to guarantee an industry-specific and accurate learning experience through sharing of perspectives and challenges.
12.10 Pharmacovigilence UDI Globally
The Role of the Company Core Data Sheet (CCDS) as a Pharmacovigilence Document
Cathrine Lang Safety Surveillance Specialist NovoNordisk, Denmark
UDI Implementation and Global CompatibilityJackie Rae Elkin Global Process Owner - Standard Product Identification Medtronic, USA
12.50 Lunch & Exhibition Viewing
Webinar: Updating and Tracking the Company Core Data Sheet (CCDS) WEBINAR
Beth A. Lage Associate Director, Global Regulatory Affairs,Regulatory Operations and Compliance – Labeling Baxter Healthcare Corporation, Inc., USA
UDI from Theory to Labelled ProductVirginie Siloret Head of Quality, E.M.S. Electro Medical Systems S.A., Switzerland
14.15
14.55 Brainstorm Session: Discovering the Best Approach Strategy to Company Core Data Sheets (CCDS)Facilitator:
Amer Alghabban Quality Assurance Adviser, Polyphor AG, Former Global Head, Director QA Merck Serono, Switzerland
Case Study: Implementing UDI in a Small-Medium Sized Global Company
Kaja Tengbjerg Senior Regulatory Affairs Professional Ambu, Denmark
15.35 Afternoon Tea & Exhibition Viewing
Company Core Data Sheets (CCDS) Globally Post Market Surveillance
16.05 Webinar: Dealing with Company Core Data Sheet (CCDS) When Working in Different Countries
Leander Fontaine Managing Director Pharmiceutics Labeling Services LLC, USA
UDI Implementation and Post Market Surveillance Laura Locati Regulatory Compliance and Quality System Director EMEA Abbott Vascular, Italy
16.45 Applying the CCDS to the Japanese Package InsertStewart Geary Chief Medical Officer & Senior Vice President Eisai Co., Ltd., Japan
Industry Feedback on the Pilot of the Revised Manufacturer Incident Reporting Form
Marta Carnielli Manager, Safety Risk Management & Surveillance Ortho Clinical Diagnostics, France
17.25 Closing Remarks from the Chairperson
17.30 End of Day 3
Day Thursday 29th October 20153
To register or for the latest information, please visit: www.pmdlsummit.com Tel: +44 (0)20 7017 7481 Email: [email protected]
WE BIN AR
To register or for the latest information, please visit: www.pmdlsummit.com Tel: +44 (0)20 7017 7481 Email: [email protected]
The Pharmaceutical and Medical Device Labelling Summit
UDI Regulatory Experiences World Café
Register 18.15 • Start 18.30 • Finish 20.30 • An evening networking dinner will be provided
This interactive break-out session will allow attendees to discuss particular challenges encountered with the implementation of UDI in an informal environment. Hear delegates share their anticipations and current state of play in their respective regions. Benchmark best approaches and strategies to prepare for UDI implementation and get your questions answered before joining another café table. World café tables will include:
Exploring Labelling Strategies Globally
Register 18.15 • Start 18.30 • Finish 20.30 • An evening networking dinner will be provided
This workshop provides a comprehensive understanding of labelling strategies and labelling regulation developments outside of the EU. Gain the opportunity to analyse and asses the similarities and difference between EU and the rest of the world. Optimise your success in entering these markets and hear success stories that could benefit your organisation.
Understanding The Falsified Medicines DirectiveRegister 18.15 • Start 18.30 • Finish 20.30 • An evening networking dinner will be provided
The Falsified Medicines Directive aims to target the increasing and ongoing threat to public health and safety of the circulation of falsified medicines. The directive affects all levels of the supply chain and inflicts manufacturers with numerous obligations. This workshop aims to clarify and strengthen your understanding of The Falsified Medicines Directive to ensure correct compliance, reduce the risk of decreased sales as well as address the below points:
• How far along are we in the project and what lies ahead?• How will the directive affect your workplace • Strategies for implementation• How will this affect countries outside the EU?• Exploring rulings coming in or already in place worldwide
to stop the trade in falsified medicines
Workshop leader: Amer Alghabban, Quality Assurance Adviser, Polyphor AG, Former Global Head, Director QA Merck Serono, Switzerland
Points to consider: • Do you completely understand the proposed regulations?• Are all stakeholders fully committed and aligned? • Are you prepared for the vast amounts of collection and
aggregation of regulatory data?• Do you understand the impact of UDI implementation on
your company’s operations?
Table 1: UK
Andrew Rutter, Regulatory Affairs Associate, Ortho Clinical Diagnostics, UK
Table 2: North America Jackie Rae Elkin, Global Process Owner - Standard Product Identification, Medtronic, USA
Table 3: Rest of EuropeGéraldine Lissalde-Bonnet, Public Policy Senior Manager, GS1 Global Office, Belgium
Each region specific session will address the following:
• The regulations in place for medical device labelling • Recent developments in regulation on medical devices• Case studies including best strategies and approaches to
dealing with multiple labelling requests• Key challenges and how these are overcome• Future developments for these regions
Session 1: US, CanadaRob Bergman, W. L. Gore & Associates, Inc. Packaging & Labeling, USA
Session 2: ChinaMaike Eva Kaae, Regulatory Affairs Specialist, Radiometer, Denmark
Session 3: India & ASEAN countriesMohan Umale, Assoc. Manager Regulatory Affairs, Stryker Global Technology Center, India
Session 4: Russia and CISAlexey Stepanov, Regulatory and Quality Assurance Manager, Sorin Group, Russia
Free with med dev
UDI day pass
Evening Seminar and Networking Dinner: Wednesday 28th October 2015
Evening Seminar and Networking Dinner: Wednesday 28th October 2015
Evening Seminar and Networking Dinner: Thursday 29th October 2015
Pharmaceutical Labelling and
Company Core Data Sheets
Labelling Compliance and
UDI Implementation for Medical Devices
and IVDs
1 event: 2 streamsThe Pharmaceutical and Medical
Device Labelling Summit
To register or for the latest information, please visit: www.pmdlsummit.com Tel: +44 (0)20 7017 7481 Email: [email protected]
The Pharmaceutical and Medical Device Labelling Summit
Sponsorship & Exhibition Opportunities
Sponsorship benefits include:
• Create a networking base at The Pharmaceutical and Medical Device Labelling Summit. with an exhibition stand in the main networking area, providing your team access to the whole audience; an opportunity to meet new clients and touch base with existing clients
• A speaking slot on the main programme giving your company the chance to showcase its expertise
• Logo visibility with branding packages that ensure that your company logo is seen by all of our attendees
• Networking drinks
Exclusive Opportunities:
• Lunch Sponsorship Raise your corporate profile, branding and exclusivity by hosting the delegate lunch which provides an opportunity to informally address the audience and network in a relaxed environment
Quick-fire Technology Showcase: Demonstration of the Current Software on the Market to Assist Data Management
We are looking for rising stars to showcase some of the latest labelling technologies. Each service provider will take the limelight for 15 minutes,providing a short and snappy summary of some emerging technologies in labelling as part of this interactive session.
Have you got the tech factor? If you are interested in presenting on this topic please contact Linda Cole: Email [email protected], Tel: +44 (0)20 7017 6631
• Chairing the event Demonstrate your company’s status and lead the audience
through the day’s programme whilst sharing your expertise by leading questions following individual presentations
Sponsored webinars
Take advantage of this new for 2015 opportunity to broaden and strength your target audience by showcasing your latest technologies and solutions to a global scale audience. This unique opportunity allows for a flexible arrangement for both vendors and customers.
,,
“
Sponsors and Exhibitors for 2015
Media Partners
Contact: Linda Cole Email [email protected] Telephone +44 (0)207 017 6631
27th – 29th October 2015 Maritim proArte Hotel Berlin, Germany
This was an excellent event. As a sponsor and speaker, I met many new contacts and it offered a perfect match for the companies we were looking to meet.Business Development, Schema
As a first time exhibitor at the Informa Labelling event, I was very impressed with it. We made far more new contacts than expected. This was a great platform for the future and I highly recommend it.mt-g medical translation GmbH & Co. KG
To register or for the latest information, please visit: www.pmdlsummit.com Tel: +44 (0)20 7017 7481 Email: [email protected]
The Pharmaceutical and Medical Device Labelling Summit
FACTS & FIGURES
Contact: Linda Cole Email [email protected] • Tel +44 (0)207 017 6631
over 100 different companies attended in 2014
and
with 60% being Manager-level & above
20 top
100 companies attended in 2014
Make sure you bring plenty of business cards as we are introducing speed networking
2015...
Did you know....
2014 STATS
CEO level 12%
Director 12%
Head 8%
Manager 34% Labelling professionals34%
47%
15%
10%
5%
6%
4%
2%2%
2%2%2%2% Regulatory
Director
Labelling
Manager Medical A�airs Project
Drug Safety Pharmacology Pharmacovigilance Product information Safety
Consultant
Past Pharmaceutical
Labelling Audience
Breakdown
44%
14%
9%
5%
6%
6%
3%
3%2%
2%2%
2%2%2%Regulatory Labelling Artwork Manager Quality Marketing Technical UDI Business Development Consultant Director Documentation Operations Packaging
Past Medical
Device Labelling Audience
Breakdown
27th – 29th October 2015 Maritim proArte Hotel Berlin, Germany
Where did the delegates come from in 2014?
40%
2%
2%
2%
2%
4%
13%
8%
6%
6%
8%6%
Our audience is interested to meet solution providers in the following areas:• Translation
• Readability testing /User testing
• Proofreading
• Structured content management
• Folded labels and labels in general
• Change control
• Software solutions
• Product information management software
Take advantage of our extensive database of labelling professionals:
+9000 Labelling contacts +700 Average unique pages
views per month in 2014
USA
Northern Europe
Southern Europe
3 Easy ways to register+44(0) 20 7017 7481
www.pmdlsummit.com
For group booking discounts please ring: Michael Dunnet, Tel: +44 (0) 20 7017 7870 Email: [email protected]
Conference Documentation: Cannot Attend? For those busy executives who cannot take full advantage of this event, the papers give you a useful record of the presentations made at the event. The set of speakers papers and/or slides from the conference is available after the event for £499 + 20% VAT. Contact Customer Services on tel: +44 (0) 20 7017 7481, fax: +44 (0) 20 7017 7823 or email: [email protected].
Terms and ConditionsFEE: this includes all technical sessions, refreshments, lunch and access to speakers’ presentations that we have permission to make available.CANCELLATIONS: Cancellations received in writing before and on 13th October 2015 will be subject to a service charge of £99. The full conference fees remain payable after 13th October 2015. Substitutions are welcome at any time. It may be necessary for reasons beyond the control of the organiser to alter the content and timing of the programme or the identity of the speakers. In the unfortunate event that an event is cancelled Informa are not liable for any costs incurred by delegates in connection with their attendance. This contract is subject to English Law.ARE YOU REGISTERED?: You will always receive an acknowledgement of your booking. If you do not receive anything, please call us on +44(0) 20 7017 7481 to make sure we have received your booking.Due to unforeseen circumstances, the programme may change and Informa reserves the right to alter the venue and/or speakers. ©Copyright Informa BV, 2015. Yes I agree to the terms and conditions as stated on this form.
DATA PROTECTION: The personal information shown on this form, and/or provided by you, will be held on a database and may be shared with other companies in the Informa Group in the UK and internationally. If you do not wish your details to be avaialble to companies in the Informa Group please contact the Database Manager at Maple House, 149 Tottenham Court Road, London, W1T 7AD., Tel : +44 (0)20 7017 7077, Fax: +44 (0)20 7017 7828 or email: [email protected]. Occasionally your details may be obtained from, or made avaialble to, external companies who wish to communicate with you offers related to your business activities. If you do not wish to receive these offers, please tick the box INCORRECT MAILING If you are receiving multiple mailings or you would like us to change any details or remove your name from our database, please contact the Database Manager at the above addresss, Tel: +44 (0)20 7017 7077, Fax: +44 (0)20 7017 7828 or email: [email protected] - quoting the reference number printed on the mailing label.ANY SPECIAL REQUIREMENTS: Please inform us if you have any special requirements by calling Customer Services on +44(0) 20 7017 7481.
Head of Department:E-mail
Tel FaxBooking ContactE-mail
Tel FaxName of Company/Department
Address
City PostcodeCountry Tel FaxVAT Customer Number Nature of Company Business No. of employees on your site: 1) 0-49 2) 50-249 3) 250-499 4) 500-999 5) 1000+
(Mr/Mrs/Ms/Miss/Dr) Family NameE-mail
Tel Fax
ForenameJob TitleAny special requirements?
To assist us with future correspondence, please supply the following details:
DELEGATE DETAILS – Please photocopy form for multiple bookings!
Venue Details: Maritim proArte Hotel Berlin, Friedrichstrasse 15110117, Berlin, GermanyPhone +49 (0) 30 2033-5 Fax +49 (0) 30 2033-4090 Reservation phone +49 (0)30 [email protected] http://www.maritim.com/en/hotels/germany/proarte-hotel-berlin/hotel-overview
ACCOMMODATIONReduced rate accommodation: delegates are responsible for the arrangement and payment of their own travel and accommodation. Informa has negotiated a special room rate at the event venue and a number of hotels nearby, to take advantage please visit the “Accommodation” page of the conference website: www.pmdlsummit.com Please book early to avoid disappointment www.pmdlsummit.com
27 – 29 October 2015 • Maritim proArte Berlin, Germany www.pmdlsummit.com
To make payment by credit card: to ensure we provide the highest level of security for your credit card details we are unable to accept such payments via email or fax which ensures that these details are never stored on our network. To make payment by credit card on-line, please enter your credit card details in our secure payments website that you will use when making your booking via the event website (the event web address is near the top of the booking form). Alternatively call our customer service team on +44 (0) 20 7017 7481.
CQ5254
@Informa_Regs #pmdlsummit
Pass Book before 7th August 2015 SAVEBook between 7th August 2015
and 25th September 2015SAVE
Book after Friday 25th September 2015
Save
1 day pass plus seminar only for the med dev UDI day*
£1098 + VAT £200 £1198 + VAT £100 £1298 + VAT - 2 day pass £1399 + VAT £200 £1499 + VAT £100 £1599 + VAT - 3 day pass £2198 + VAT £200 £2298 + VAT £100 £2398 + VAT -
Upgrade your pass to include an Individual Evening Seminar* (can only be booked as part of a 2 or 3 day pass)
£499 + VAT
Tuesday 27th October 2015
PHARMA LABELLINGOR
MEDICAL DEVICE
Understanding The Falsified Medicines Directive Exploring Labelling Strategies Globally
Thursday 29th October 2015
MEDICAL DEVICE
UDI Regulatory Experiences World Café
* VAT at 19% - The VAT rate is subject to change and may differ from the advertised rate. * T&c’s: Workshops and Seminars are only sold in conjunction with a conference pass. Discounts cannot be accumulated. * 1 day pass T & Cs: One day pass only applies to UDI day. SMALL/START UPS: 50% off the current price tier.Only apply to 2 days pass .Does not apply to vendors or suppliers. Informa Life Sciences will verify whether you are a vendor/supplier when your registration is processed. ACADEMIC: Applies to a 2 day pass. Informa Life Sciences will verify whether you are considered an Academic.
The Pharmaceutical and Medical Device Labelling Summit
ACADEMIC FLAT RATE
£499
( 2 day conference pass) * T&C’s Apply
SMALL BUSINESS / INDUSTRY START-UP
50% off*
current price tier