GUARANTEED TO ENSURE YOU ARE READY TO MEET ALL THE SERIALISATION REQUIREMENTS!
The FMD is fast approaching and with that urgency, key questions have arisen from the pharma industry:
If you relate to any of these questions above then this conference is for you! With time now not on our side, it is important to prepare for serialisation now before it is too late. This conference has been designed with you in mind – to ensure you will be entirely prepared for the FMD and will meet all serialisation requirements!
Over three days of exclusive case studies, workshops, round tables, panel discussions and informal networking, we will bring together serialisation experts from across the industry to discuss how to meet the different regulations and how to make the final changes to meet the regulatory requirements of the FMD!
In 2018 we are co-locating with our industry leading Pharmaceutical Packaging and Labeling Conference. Further your understanding on adhering to regulations, patient safety, tamper evidence as well as building brand recognition as ONE pass gets you access to BOTH conferences. So grab a colleague and book your package now!
With Discussions and Presentations Hosted By:
Head Supply Chain Management
Principal Advisor Pharma Digitalisation
Epista Life Science
DSM Sinochem Pharmaceuticals
Director, Corporate Projects
Global Director, Program Management Office
Liaison Regulatory and Government Affairs
National Policy Liaison
Medicines for Europe
Supply Chain Manager
Associate Director Global Regulatory Affairs
Senior Consultant Healthcare
Sr.Director Global Supply Chain Quality
Process Design & Digitalization , Global Manufacturing Pharmaceuticals
Manager Logistics & Export
What Will You Learn At The 2018 Forum?
Hear case studies from Getz Pharma and DSM Sinochem Pharmaceuticals on their serialisation strategies
GS1 share how the EU should be preparing for the FMD and final considerations that need to be made
Hear from Abbot on how to meet the serialisation requirements in emerging markets
Learn how to advance your packaging lines as Fresenius share how they brought innovation to their packaging lines
A panel discussion led by R-pharm and Arena Pharmaceuticals on how to prepare for Serialisation as a CMO
Join round table discussion led by Sanofi Genzyme, Fresenius-Kabi amongst others on topics ranging from preparing for the FMD to managing serialisation data
What Others Have to Say
“The diversity of speakers is making the event really valuable.”Jean-Luc Lasne, Alliance Director – Automation, Adents
"Very insightful on how other companies struggle with the same issues, and how solution providers deal with the struggle."Wolfram Gönner, SAP Specialist Track & Trace and Logistics, Octapharma GmbH
“It enabled me to connect with peers and vendors, gain some knowledge on where we all stand with regards to serialization delivery”Raffaelli, PMO Manager, Nestle Skin Health
“Very valuable, especially the networking”Pasi Kemppainen, Exec Consultant, NNE
“This has been very helpful to have insights on possible mistake and most important aspects to focus on during implementation”Edouard Chapuis, Information Quality Assurance Manager, Infomed Fluids
“Good playground for networking“Michael Unbehaun, PM, R-Pharm
“Speaker panel was perfect. Conferences were all interesting”le Mintier Supply Chain Manager Provepharm
Serialisation Track and Trace Map 2018
By 2020, serialisation is expected to cover 80% of the global drug supply, but disparity between regulations in different parts of the world means high costs and complexity for companies in the supply chain. As global deadlines loom, we have created this printable map to provide an overview of various nations journey to serialisation.
Acceleration, Optimisation and Beyond Compliance
Pharma IQ spoke with experts in the industry to discuss moving beyond compliance in serialisation and their predictions as to how successful the regulations will be at reducing the presence of counterfeit pharmaceuticals on an international scale.