Next-Gen Clinical Trials Forum

The recent progress of sciences and improvement of regulations drives development of new generation of diagnostic equipment and treatments, impacting the growing need in the clinical trials and their personalization for the needs of clients. Augmenting evolution in technology and growing demands of CROs are opening doors to globalization of clinical trials. On the other hand, Developed & developing nations are also coming together to solve challenges with new and innovative ideas through streamlining and digitizing clinical trials.

Against this background, Next-Gen Clinical Trials Forum 2020 scheduled for 22nd & 23rd April in Tel-Aviv, focuses on the challenges of clinical trials such as reducing the timeline for trials, standard procedure of patient recruitment and introducing new technologies in this field foreffective and accurate data management.

The conference will also aims to provide a multidimensional overview of the industry environment of USA, Europe & developing countries like India to enable the sharing of theirs clinical trials experience, discovering new area of collaboration thereby creating a rippling effect in this field.

Key Sessions

  • Updates on Regulatory Affairs & Strategies
  • AI & Tech Driven Trials for Real Time Analysis
  • Big Data & Clinical Data Strategy
  • Patients Recruitment, Engagement & Retention
  • Strategic partnerships & budget Management

Program Committee

Who Should Attend

This conference is tailored for professionals from:

  • Pharmaceuticals
  • Medical Devices
  • Biotechnology
  • Start-ups
  • CROs
  • Consultants/Freelance/CRAs
  • Hospitals & Universities
  • Solution Providers

with responsibilities in the following areas:

  • Global Regulatory Affairs
  • Quality Assurance/Quality Control/Quality Compliance/Quality Management
  • Clinical Operations/Research/Planning
  • Clinical Outsourcing and Development
  • Records/Data Management
  • R&D Operations
  • Trials Management/Research
  • Global Compliance
  • Risk-Based/Centralised Monitoring
  • Safety and Risk Management Operations
  • Site Performance Management
  • Internal/External Auditing
  • Clinical Project Management
  • Clinical Documentation Management
  • Pharmacovigilance
  • Business Development
  • Marketing

Why Should you Attend

  • Gain perspective on the updated regulations
  • Understanding the GCP compliance & FDA approvals
  • Understanding perspective of other nations for effective partnership
  • Reconnoitre AI and Wearable Devices for effective & real time data capture
  • Explore the new dimension of data storage & data management through Big Data
  • Understanding effective digital strategy for patient engagement, enrolment and retention
  • Identifying effective procedures & strategies for selecting the right partner for cost effective clinical trials Effective Data security & integration of Clinical data in cloud environment

Facts You Should Know

25+ Industry expert speakers from public and private sectors
150+ Attendees
7+ Hours of Networking
Focused Sessions Presentations from international speakers

Registration

The conference fee includes*

  • All conference sessions
  • Lunches and refreshments
  • Access to exhibition room
  • Networking breaks
  • Conference workbook