Personalized Medicine World Congress 2022 Europe

Transformative Capability of Personalised Medicine in Improving Health Outcomes

London, United Kingdom
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precision for medicine

Precision medicine (PM) is a medical model that proposes the customization of healthcare, with medical decisions, treatments, practices, or products being tailored to a subgroup of patients, instead of a one‐drug‐fits‐all model

  • Introduction
  • Insight
  • Who Should Attend

Personalised Medicine World Congress 2022 Europe, London, United Kingdom

Introduction

Personalised medicine is a new tailored healthcare approach which is based on each patient’s unique genetic makeup as opposed to traditional medicine. It is a next-generation of treatment, which aims to advance the management of patients’ health by individualization to achieve the best outcomes in disease prevention, diagnosis, and treatment, and for the management of a patient’s condition, their predisposition to disease, and their prognosis. Following the development and deeper understanding of genetics and human genetic makeup, medical professionals are now able to develop safer and more effective treatment methods and drugs for various health conditions. This includes acquiring and examining patient health data to interpret scientific advances in disease research in order to enhance the quality of patient care.

The Personalised Medicine World Congress will focus on the “Transformative Capability of Personalised Medicine in Improving Health Outcomes”.

The Congress aims to look at the future of medicine in the digital age, the new challenges brought about by the pandemic, the role of technology moving forward, patient empowerment, ethical, social & legal issues surrounding patient information, cost, underdevelopment of technologies needed to meet the goals of precision medicine, lack of knowledge about molecular genetics and biochemistry, and reimbursement issues. We will explore how collective intelligence and collaborative leadership can drive innovation, as well as the need to change the culture in healthcare to be more patient-centered, participatory, and safety-focused.

According to Adroit Market Research, Personalized Medicine Market to Reach USD 800 Billion by 2028 at a CAGR of 7%. Massive advancements in companion diagnostics, improved funding schemes from private and public institutions along with technological development such as AI integration are steering large-scale growth in the personalized medicine market.

Although global personalized medicine is at a competitive edge, it is grappling with several challenges that are likely to hamper the growth of the global personalized medicine market. Nevertheless, rising interest in biomarkers, developments in genomic sequencing, expansion of precision medicine in health and healthcare areas, and advancements in biomarker analysis are promoting the development of the global personalized medicine market.

The two-day Congress will provide an interactive, cutting edge and comprehensive discussion and networking format led by international renowned speakers bringing their expertise on patient preferences, data harmonisation, implementation of personalised medicine into the healthcare system, collaboration between academia and industry, and the value of personalised medicine to patients.

We look forward to welcoming you to the congress!

Personalised Medicine World Congress 2022 Europe, London, United Kingdom

Gain Latest Insights on:
 
  • Where the future of medicine is really taking us.
  • Discussions around digital rights/data ownership/governance
  • Ai and digital technologies, will they help us or hurt us? Addressing bias in technology
  • Changing the Pharma mentality and adapting to the McKinsey mindset.
  • Looking at healthcare from a global perspective and building a better ecosystem
  • Technological advances in sequencing, improved knowledge of omics, integration with bioinformatics, and new in vitro testing formats
  • Best practices, current diagnostics, and therapeutic clinical guidelines in personalised medicines research
  • Emerging opportunities in personalized medicine, cutting-edge new strategies, and solutions
  • Realising the basis for current effective targeted therapies in disease, based on molecular, environmental, and patient lifestyle factors.
  • Enhancing education and literacy of every component and stakeholder of the personalised medicine ecosystem
  • Developing further collaborations and initiatives
  • Facilitating innovation and transfer of scientific knowledge
  • Implementing personalised medicine towards sustainability

Personalised Medicine World Congress 2022 Europe, London, United Kingdom

Who should attend:
 
This congress is specially created for valued stakeholders and decision-makers  in Personalised Medicine’s community:
  • Personalized Medicine and Diagnostics
  • Clinical Research and Development
  • CMC, Quality Assurance
  • Biomarker Research Scientists and Developers
  • Emerging ‘Omics Diagnostics in Genetics/Genomics
  • Proteomics/Protein-based Assays
  • Artificial/Augmented Intelligence
  • Informatics, Analytics, Imaging platforms
  • Legal,  Policy, Regulatory, and Business Affairs
  • Systems Developers for Systems and Software
  • Submissions
  • Pharma & Biotech Industry
  • Healthcare professionals
  • Big data scientists
  • Commercial and Operations
  • Payers and Insurers
  • Patients and Patient Groups
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Key Industry Expert Speakers

Meet Our Professionals

Christine Von Raesfeld

Founder & CEO

People with Empathy, USA

MARTIN BRUNNINGER

Director General

Department of Health & Social Care for Austria

Igor Rudychev

Vice President, Enterprise Analytics

Horizon Therapeutics

Carole Scrafton

CEO & Co-Founder

FibroFlutters

Prof. Maria José Alonso

Editor-in-Chief

Drug Delivery and Translational Research

Dr. Svetlana Mukhina

CDx Global Regulatory Lead, Assoc. Director Global Regulatory Affairs, CDx

Merck

Esther Mahillo

VP, Operational Strategy,

Precision for Medicine

Milan Mishkovikj

Vice President of the Alliance of Patients

Organizations in N.Macedonia – APO

Coming Soon

Senior Representative

Available Shortly

Schedule

Our Conference Production Team are now at the final stages of the overall complete program agenda - which will be available below shortly. 

  • Day 1 - Monday21/11/2022
  • Day 2 - Tuesday22/11/2022
  • Auditorium 1

CHALLENGES & TRENDS IN THE DEVELOPMENT OF PERSONALISED MEDICINE

  • Importance of individual and public engagements
  • New skills for healthcare professionals and novel tools for delivery
  • What must be done for the successful implementation of PM in all perspectives?
  • The use of health related data
  • How to develop sustainable economic models that allow improved therapy, diagnostic and preventive approaches as new healthcare concepts for the benefit of the public?
  • How can personalised medicines revolutionise the traditional healthcare and treatment approach?
  • To exploit the benefits of personalised medicines, what challenges must be addressed?
  • Implementation of the precision medicine approach to design highly targeted therapeutic drugs
  • At this stage, is awareness and education amongst all the stakeholders and regulatory support from governing bodies as well as policymakers enough to progress?
  • Benefit, risk evaluation and regulatory decision making
  • Emerging new clinical trials design
  • Use of data derived from several independent studies
  • HTAs acceptance
  • How to prepare for and adopt rapid shifts in regulations related to personalized health care?
  • How to streamline regulatory processes to reduce unnecessary burdens associated with regulatory activities
  • Advantages of taking a data-centric approach
  • What are the life-changing potential of  personalised medicine in improving health outcomes?
  • What are the role of clinical research in facilitating personalised medicine development?
  • Best practices and lessons learned for timely access to the targeted population

TECHNOLOGIES, INNOVATIONS & CLINICAL TRIALS

  • Advancements in wearable and digital therapies
  • Universal adoption and accessibility of wearable and digital technology
  • What are the major drawbacks and areas for improvement?
  • Addressing issue in privacy protection: data generated or stored by commercial wearables.
  • Astonishing potential of AI in assisting clinical decision making and revolutionizing the field of health care.
  • Different sources of biases for machine learning algorithms
  • Tools that can help address biases in AI
  • Current challenges in next generation sequencing
  • What are the key benefits of Comprehensive genetic profiling?
  • Integrating comprehensive genomic profiling into real-world setting
  • Design and clinical impact of innovative comprehensive genomic profiling clinical trials
  • The pivotal role of epigenetic mechanisms in health and diseases
  • State-of-the-art epigenetic IVD tests and epigenetic drugs which are presently being established in clinical trials.
  • How epigenetic technology will support the incorporation of precision medicine in clinical settings?
  • Defining decentralized clinical trials and understanding their nuances
  • Engaging with various stakeholders early in the process
  • The importance of physicians involvement in performing the much-needed test and checks that technology alone cannot handle
  • Upcoming therapies, technologies and treatments that will enhance all aspects of patient care
  • Analytics that reduced cost to patients
  • New technology demands unified security models
  • Real-time digital integration, hospital-wide AIs, and smart medical facilities
  • Decentralized clinical trial strategies to fully integrate every aspect of the available new tech.
  • Auditorium 1

COLLECTIVE DATA AND DIGITAL AGE

  • How the focus on digital patient engagement helps healthcare providers create a greatly improved personalized patient experience from start to finish.
  • Imperative for engaging end-users in each phase of digital health design
  • Techniques to facilitate better digital health design and implementation.
  • Bridging the divide between technology companies, patients, and clinicians regarding effective development and use of digital health
  • The need to develop new, scalable and expandable big data infrastructure and analytical methods
  • The nature of big data and the role of semantic web and data analysis for generating “smart data”
  • How to create a system that makes big data robust and smart for healthcare providers and patients
  • Accessing unlimited online opportunity to learn more about diseases, seek and or give assistance.
  • Importance of finding and connecting with others infected or affected by the same illness or disease.
  • Opportunity to exchange relevant data on their condition, treatment , symptoms, side effects, etc.
  • Addressing the challenge of data protection to ‘go digital’
  • The fundamental rights to privacy and to the protection of personal data have become more important for the protection of human dignity than ever before.
  • Ethical dimension of data processing.
  • The need for a new regulatory framework, guaranteeing the rights of individuals.
  • Drivers and scale-up capabilities to advance RWD life cycle
  • Adopting the best practices and overcoming the associated challenges
  • Gauging the progress brought to downstream use by better data life cycle practices.
  • Dynamic data strategy agendas that overcome fragmentation and are representative of populations.
  • Acknowledging deterioration of public trust in the use and commercialization of healthcare data through transparency and engagement
  • Right governance in place for your critical data assets
  • Addressing patients on social media
  • Looking at issues around bluetooth hacking in medical devices
  • How does data security deal with the technical framework of keeping data secure and available?
  • How can we protect ourselves?

PATIENT EMPOWERMENT AND ACCESS

  • How can we all work collaboratively to reexamine clinical trials and increase trust, awareness and engagement.
  • The importance of embeding “patient centricity” into all aspects of a clinical trial
  • Breaking down barriers to clinical trial recruitment and retention
  • Barriers to accessing personalised medicine
  • Strategies to ensure that patients have equitable access to medicines and health care
  • Health technology assessment securing patient access to personalised medicine
  • Innovative payer models
  • Key factors influencing cost-effectiveness of personalised medicines
  • Value-based approach to inform policy decisions about reimbursement and investment in research and development
  • Societal perspective including opportunity costs, such as out-of-pocket patient costs, other indirect medical costs, also loss of income or productivity
  • How can patient centricity play a vital role to personalised medicine?
  • Understanding the paradigm for patient partnership
  • Establishing trust at every patient touch-point to achieve sustained behavior change through informed decision-making.
  • Building a more effective patient partnership  models throughout the customer’s lifecycle

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Tickets

Take Advantage of the Super Early Bird Discount. Group Discounts Also Available. 

Standard Registration Rate

Full Price
£1299
  • 2 Day Congress + Full Access
  • All Day Refreshments & Lunches
  • Congress Ducumentations
  • Networking Drinks Reception

Testimonials

what people say

From a patient advocacy organization perspective, was a very informative meeting. Learned a lot from presentations and networking that will inform how we can add value to the advocacy-patient-drug developer dialogue.
Dr. Nadine Tutton
Scientific Director, Research, Association for Frontotemporal Degeneration
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

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