clinical trial protocol design and optimization program

This program is aimed at professionals wanting to learn the principles of clinical trial protocol design and optimization using state-of-the-art, data-driven solutions.

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Data-driven clinical trial protocol design and optimization

Target audience:

This course is aimed at those wanting to learn the principles of clinical trial protocol design and optimization using state-of-the-art approaches. The day-and-a-half course consists of lecture series along with practical exercises and interactive sessions.

Trainers:

The clinical trial academy is composed of experts from academia and industry who hold operational, managerial, and regulatory clinical trial expertise. Such diversity in background and experience provides a wealth of insight into how to create a sound trial protocol.“At the end of the course, you will receive a confirmation of participation. ”

Min: 5 / Max: 12 Participants
1,900 CHF
31st October - 1st November 2022
Bern
Day 1

Clinical rial: Theory & reminder

  • Phases of clinical trials
  • Roles and responsibilities in trials
  • Role of protocol in trial conduct

Networking lunch

Clinical trial: Interactive design

  • Trial protocol: Endpoints
  • Trial protocol: Eligibility criteria
  • Protocol writing: strategy, style, and readabilities
Day 2Half-day

Data-driven trial groundwork

  • Interactive data-driven protocol design
  • Interactive data-driven protocol optimization