October
Regulatory Affairs
Strategy Meeting Europe 2022
The premier meeting for European Regulatory Affairs professionals
What makes our strategy meetings unique?
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Roundtable Discussions
Intimate discussions led by renowned industry experts. Have your voice heard and debate alongside like-minded life science executives.
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Unrivalled Networking
With senior delegation from big pharma and innovative biotech from across Europe, you can network with peers from different locations, all in one place.
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Personalised Agenda
Choose the topics that matter to you. Reserve your place at the roundtable discussions and ensure your whole day delivers the insights you need to hear.
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Solutions to your Problems
We’ve partnered with the best solution providers to solve your biggest challenges. Engage in pre-arranged, private meetings to address your specific needs and find a tangible solution.
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Industry Researched Topics
We guarantee our agenda is up-to-date and mission critical because its designed by you. We speak to our extended network of senior decision makers to ensure the most important topics are discussed.
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Senior Decision Makers
The entire strategy meeting is specifically tailored to the needs and challenges of senior life science professionals. Discover how your peers are dealing with the same challenges as you.
Meet Our 2022 Facilitators
Our panel of facilitators play a key role in shaping the agenda for the day. See who will be bringing their expertise to the table at our Regulatory Affairs meeting.
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Simon Cavanagh
Account Executive Life Sciences Esko I Brand Solutions
Beatriz Goñi
Regulatory Affairs Manager Asphalion
Klara Dalmay
Director, RA International PTC Therapeutics
Krisztian Fodor
Head of Global Regulatory Leads Gedeon Richter
Elisa Gomez-Reino Garrido
Sr Director, International Expansion, Global Regulatory and Quality Alexion Pharmaceutical
Anna Löfgren
Vice President, Head of Global Quality SOBI
Koen Nauwelaerts
Regulatory Policy and Innovation Lead Bayer
Urszula Ĺšcieszko-Fic
Regulatory Intelligence Head Gedeon Richter
Tamas Szolyak
Director Global Regulatory Science & Portfolio Management Gedeon Richter PlcSee the complete agenda and facilitator line-up
Download the strategy meeting brochure for full detailsWho Should Attend the Event?
Chief Executive Officers
Senior Vice Presidents
Executive Vice Presidents
Vice Presidents
Global Heads
Directors
Executive Director
Responsible For:
Regulatory Affairs
CMC
Safety & Compliance
Quality Assurance/Compliance
Labeling Management & Compliance
RIM & Data Management
Regulatory Operations
See Which Topics Are Discussed at the Strategy Meeting
A Comprehensive View and Vision of the Future: Exploring the Current Regulatory Landscape and Learning Outcomes from the COVID-19 Pandemic
Roundtable Tracks
1Best Practices to Create and Maintain a Global Dossier to Support Global Submissions While Handling Effectively the Local Regulatory Requirements and Diverse Authority Questions
Accelerating Development, Registration, Submission, and Market Tracking Of Globally Unified Products and Create Profound Synergy Among Global Regulatory Authorities And Pharmaceutical Industry
Structured content management as a strategically important tool to drive the transition from paper to electronic labelling information for patients and HCPs
Roundtable Tracks
2How to overcome RIM challenges from a regulatory perspective ASPHALION
Tools and Technologies to Best Communicate Robust Regulatory Strategies FOR SPONSOR
Utilizing Dynamic Labeling Management Technologies For An Effective Content Management, Workflow And Structured Authoring FOR SPONSOR
Reasons To Attend the Strategy Meeting
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Examine the current state of the regulatory landscape and explore how you can streamline complex regulatory processes throughout the product life cycle chain
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Engage and collaborate with regulatory teams, global health authorities and decision makers to reduce costly duplication effort, share experience and knowledge, optimize use of limited resources and expand capabilities
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Constructive roundtable discussions will address how leading pharma and medtech companies are driving continuous transformation and responding faster to ever changing regulatory environments
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Address the organizational, data and process challenges to streamline regulatory activities and fully benefit from an end-to-end RIM visibility
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