- 20th - 21st October 2025
- London, United Kingdom
​PATIENT ACCESS
WORLD CONGRESS 2025 EUROPE
Improving Patient Access for Better Health Outcomes and Quality of Life
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Patient meets Innovation & Collaboration
Improving Patient Access for Better Health Outcomes and Quality of Life
FACILITATE LIVE is very pleased to welcome you to our upcoming PATIENT ACCESS World Congress 2025 Europe. The two-day Congress aims to build meaningful collaborations within the industry, advocacy groups, clinicians, researchers and most importantly, patients and their caregivers.
The congress focuses on “Improving Patient Access for Better Health Outcomes and Quality of Life.”
Massive investment and advances in research and development of novel therapeutics by Pharmaceutical and Biotechnology manufacturers, has resulted in the life science industry obtaining an accelerated rise in the number of drugs that have been brought to market over the past decade.
Patient access in pharma and healthcare refers to ensuring that patients can readily obtain the necessary medications and treatments they need in a timely and affordable manner. This involves a range of activities, including negotiating pricing agreements, demonstrating the clinical and economic value of treatments, and addressing barriers to access.
Patient access also refers to the convenience with which patients can obtain medical care. This encompasses everything from appointment scheduling to health record access. This idea is evolving rapidly in the digital age. Technology is a key factor in improving efficiency and effectiveness.
Patient access is really about making sure that patients can easily get the medications and treatments they need when they need them, and at a price they can afford. This involves a lot of different things, from working out pricing agreements to showing how valuable treatments are from both a clinical and economic perspective, and also tackling anything that might stand in the way of access.
Here are some key things to keep in mind: Patient Access Schemes (PASs), which are those confidential pricing deals that help make expensive drugs more affordable, and Market Access, which is pretty much the same as patient access and includes all the strategies companies use to make sure patients can get their products. It also includes negotiating with healthcare, payers and providers to set prices and coverage, demonstrating the clinical and economic benefits of products to justify their prices, addressing barriers like financial constraints or lack of awareness, focusing on patient involvement in decisions, and recognizing that patient access is always changing with new technologies and treatments.
There are indeed several challenges such as the high costs of drugs, payer strategies that limit access, geographical barriers, regulatory hurdles, and a general lack of awareness among some patients. To combat this, companies can implement discounts, patient assistance programs, innovative pricing agreements, and digital tools.
In conclusion, patient access is complex. It needs pharmaceutical companies, healthcare providers, payers, and patients to all work together so that everyone can get the care they need.
We look forward to meeting you at the Congress!
Sincerely yours,
Jocelyn Raguindin
Conference Director
Paradigm Global Events / Facilitate LiveÂ
GAIN LATEST INSIGHTS ON:
- What does patient access mean for the pharmaceutical and life science industry?
- Patient access strategies that can lead to better health outcomes and quality of life for patients.
- Ensuring that patients receive the care they need when they need it.
- Successful strategies and best practices to successfully manage patients access in healthcare
- How to develop and execute a strategy to improve patient engagement?
- Recognizing the regulatory and clinical development framework for Patient Access
- Understanding the barriers to patient access and addressing them accordingly.
- How to predict potential barriers to launch and make plans to overcome them.
- How Pharmaceutical companies can prioritize access at every stage of the drug development process to ensure that their products reach the patients who need them most.
- Hear an overview of the market access system in place in large pharma markets
- Gain knowledge of the Market Access environment in Europe’s major markets
- A standardized and transparent process to improve the efficiency of the pharmaceutical system.
- Reducing health disparities by ensuring that everyone can receive the care they need, regardless of their socioeconomic status, geographic location, or cultural background
- How to maintain mutually beneficial ongoing partnerships between the patients and industry?
- Know how to implement a successful market access strategy and how to communicate value to stakeholders
- Hear an overview of the market access system in place in large pharma markets
- Gain knowledge of the Market Access environment in Europe’s major markets
- Global and European MA trends,
- Payer & industry perspective for better Patient access
WHO SHOULD ATTEND?
This Congress is beneficial to patients, pharmaceutical, biotech companies, researchers, physicians, patient advocacy groups, regulatory agencies, technology, and healthcare companies.
Network with Presidents, Heads/Chiefs, VPs, Directors, and Managers in the area of:
- Patient Access
- Patient Advocacy
- Patient Engagement
- Patient Support Strategy & Insights
- Equity, Diversity and Inclusion
- Patient Outcomes
- Medical Affairs
- Commercialisation
- Market Access
- Health Economics and Outcomes Research
- Regulatory Affairs and Policy
- Clinical Research and Development
- RWE, and Data Management
- Data Science, Technologies and Analytics
- Technology Science and Development
- Clinical Trials Management
- Payer Relationship Management
- Drug Pricing
- Reimbursement
- Health Technology Assessment
- Product and Value Strategy
- Quality and Compliance
- Epidemiology
- Programme Management
- Supply Chain Management
- Digital Patient Experience
- Digital Technologies
- Wearables
- Clinical Operations
- Clinical Insights and Experience
- Site Collaborations and Management
- Patient Diagnosis
- Pharmacy
- Business Development
- Quality and Compliance
- RWE, and Data Management
- Regulatory Affairs and Policy
- R&D Patient Engagement
- Medical Affairs
- Patient Support and Patient Engagement
- Patient Services
- Engagement Strategy
- Digital Patient Experience
- Digital Technologies
- Wearables
- Clinical Insights and Experience
- Site Collaborations and Management
- Patient Diagnosis
- Pharmacy
- Business Development
- Quality and Compliance
- RWE, and Data Management
- Regulatory Affairs and Policy
- R&D Patient Engagement
- Patient Support and Patient Engagement
- Patient Services
- Engagement Strategy
- Medical Affairs, Global Patient Advocacy & Alliances
- Government Policy and Advocacy
- Digital Patient Experience Lead
- Clinical Operations
- Clinical Insights and Experience
- Head of Strategy, Access Services
- Vice President, Site Collaborations and Patient Centricity
- Head of Neuroscience
- And much more...
Key Industry Expert Speakers 2025
We have been Gathering over 50 + Key Industry Expert Speakers
Schedule - Full Program will be Available Shortly
Content Rich Program Agenda! Featuring Keynote Presentations, Stream Sessions, Panel, and Round Table Discussions.
TRENDS & STRATEGIES IN PATIENT ACCESS
- Ensuring that patients can access products in a timely and affordable manner.
- Need to have access to data and insights early and often to make informed decisions about how pharma and biotech companies get their drugs to patients
- Digitizing healthcare to improve patient access
- Demonstrating cost-effectiveness of the product
- What is most important to patients?
Moderator:
Panelists:
- Primary barriers why patients struggle to access the therapies they need
- Proactive steps life sciences companies can take to address these barriers
- Impact of not overcoming patient access hurdles
Steve Clark, Founder and Patient Advocate, Strive for Five
- How can we seize this opportunity to improve patient access to medicines?
- Assessing the impact of the regulation on national HTAs
- Strategic implications for health technology developers
- Its influence on price and reimbursement negotiations.
- Meeting growing demands for rigorous data requirements
- Understanding of increasingly diverse environment
- Strategic and adaptive approach in navigating complexities of different ecosystem
- Breaking down silo mentality
- Harmonizing access needs and aligning strategies at an early stage
- Advancing landscape and drivers in medical devices
- The importance of early and continuous stakeholder engagement
- How multi-stakeholder collaboration streamlines the path to market and guarantees that medical devices are thoroughly designed, tested, and deployed.
- Significance of patient-centered design on market access
- Prioritizing patient needs and preferences to enhance patient outcomes
- Adopting tech-powered tools that enables to have a more direct relationship with HCPs and the patients they serve
- Innovative technologies that make patient-focused approaches scalable and efficient
- Innovative steps to improve access strategy by interacting with PAGs
- Best practices while interacting with PAGs in order to guarantee efficient cooperation and patient needs alignment.
- Integrating patient insights to improve the acceptance and relevance of health innovations
- Overcoming challenges interacting with PAGs
KEY ASPECTS TO PATIENT ACCESS
- Key trends that will affect the European biopharmaceutical market access landscape
- Impact of both the EU’s industrial pharma policy and the health technology assessment (HTA) landscape
- Overcoming the increasing constraints on government healthcare budgets
- Fundamental policy changes affecting the industry
- Breaking down silos for comprehensive strategy to anticipate challenges and opportunities in both short and long term
- Addressing urgent policy changes and stakeholder concerns while planning for the future
- Integrating patient-centricity into the broader patient access strategy
- Harmonisation imperative for sustained growth
Katja Berg, Global Value and Access Strategy, BBU, AstraZeneca
- Varying framework in place to improve patient access to innovative medicines
- Considerations for a suitable pharmaceutical regulatory and clinical framework
- How regulation can help to unlock the potential of innovative medicines
- Streamlined regulatory framework bringing breakthroughs to patients faster
- The role of IEP in drug development
- Integration of various analytical techniques
- Challenges in implementing IEP
- Evolving role of real-world evidence is emphasized, advocating for IEP
- Bullet points to follow
Marta Contente, Sr Director, Pipeline Head of Immunology, GHEVO, TEVA
- Addressing the payer activation and reimbursement challenges
- The impact of regulatory roadblocks and competition
- Overcoming the issue on inadequate market adoption by HCPs
- Patient engagement and adoption challenges
- Ensuring that patients have access to the right treatments at the right time and fair price that aligns with the effectiveness of a drug in treating disease
- Establishing pricing and reimbursement sustainability for both the pharmaceutical manufacturer and the healthcare payer
- Incorporating patient input to ensure that their drugs address the specific needs, preferences, and quality of life concerns of patients.
- Collaborative, patient-centric care approach that enhances the quality of life for patients with complex chronic conditions
- Removing barriers to treatment and improving patient access to essential therapies.
CHALLENGES & OPPORTUNITIES
- Understand the cause of health inequalities and how they affect the community
- Causes of health inequalities
- How do health inequalities impact health and wellbeing?
- How companies can address health equity through people and patient engagement;
- Success measures of efforts to advance health equity
- What can the industry do to promote health equity in the future?
Moderator:
Panelists:
- An introduction to the Access to Medicine Foundation and what we do (as we understand not everyone may be familiar with us).
- A discussion on the decreasing focus on R&D for diseases that affect LMICs and how pharma pipelines have changed over the last decade and what this means for access.
- Key insights from the 2024 Access to Medicine Index on clinical trials and access planning.
- Practical examples and recommendations on how companies can help close these gaps in access.
Sjors van Gijzel, Researcher, Access to Medicines Foundation
- Presentation of a mixed-method study findings
- How to use the findings with a range of different stakeholders
- Learnings from the initiative and next steps
Victoria Hayes, Director Public Affairs, Northern Cluster, Kyowa Kirin
- Discover how telehealth can make healthcare more accessible
- Understanding patient perspectives on telemedicine crucial for its adoption and efficacy.
- Key recommendations for telemedicine optimization and equity
- Continuous evaluation and adaptation essential to address technological challenges and disparities in telehealth usage
- Using artificial intelligence (AI) to address barriers to Patient Access
- How can data and AI be utilised to promote access?
- How can AI tools make it easier and more affordable for patients to receive needed care?
- Potential to revolutionise the healthcare industry further
- Importance of early consideration and integration of RWE into market access and commercialization strategies
- How and where to access real-world Data?
- Leveraging existing data sources and technologies to enhance study quality and streamline processes
- Robust planning and interpretation methods for effective utilisation of data for driving evidence-based decision making
- Addressing the shifting regulations
- Payer revenue optimization strategies
- The need for a 360-degree perspective across the drug development life cycle,
- The promise of real-world data (RWD) to address complex challenges
- Encourage shared decision-making to help patients feel more empowered and make informed choices.
- Open and clear communication between patients and providers to build trust and understanding.
- Educate patients to ensure patients understand their treatment plan, medications, and diagnosis
- Use innovative technology to improve the patient experience
Katherine Taylor, Patient Advocacy Lead, Pfizer UK
- Recommendations to enhance value assessment and recognition
- Strategies to improve implementation
Optimising the benefits of value-based pricing, through complementary tools
- Understanding the intricacies of pharma reimbursement
- Reimbursement hurdles that impact market access of launching new therapies and patient access
- The impact of Health Technology Assessment in reimbursement
- A successful pharma reimbursement strategy
- Future trends in reimbursement
- Addressing the unequal access to medicines for patients across Europe
- Disparities in the time it takes for European patients to access new medicines persist
- Factors causing delays and barriers to access
- Stakeholders collaboration towards pragmatic solutions that work for patients and help address Europe’s health inequalities.
Moderator:
Panelists:
- Robust market access strategy to help ensure that pharmaceutical innovations benefit the widest population possible
- Rigorous, proactive methodologies to support reimbursement
- Effective approach guided by patient-centricity to ensure patients receive timely treatment.
- Continuous medical education resulting in better clinical outcomes for patients and improved physician performance
Moderator:
Panelists:
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Testimonials
what people say
Thank you for a good experience with the PARADIGM Global Events…
very high level, very good Organization, we overpassed our expectatives, we will be pending for another congress related to pharmaceutical and biotech… we learned a lot, and i think that the content of agenda was state of the art, thank you again.
Salvador Berrios
ERP/ CRM / Product Configurator Manager
The consistently high quality of international faculty was most impressive. It was also obvious that they were carefully chosen not only for their particular expertise but also for their ability to communicate the subject matter to clinical and non-clinical participants alike. As market access consultant for pharma clients of various sizes, I now feel much better prepared to explain the nuances & dynamics involved in bringing their products to market. In addition, I am in a much better position to intelligently advice my clients & help them set realistic expectations
Thomas Martin
Associate Vice President, VCGA - Quintiles
I was impressed with the organization of this event. I attend many conferences per year and find the organizers on site to be detached and not focus on good service to the delegates. This team was even providing weather forecast warning to ensure everyone was aware and made appropriate plans. Well Done.
Adriana E. Manzi
PhD, Managing Director, Atheln, Inc
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- London, United Kingdom
- info@paradigmglobalevents.com
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