Toxicology, ADME & Early Drug Development Plan

  • Mar 2025

Description

Toxicology, ADME & Early Drug Development Plan is a conference dedicated to building an integrated safety testing strategy based on adme and toxicology.

Topics
  • Lead Optimization to application for First in Man (FIM) clinical trials
  • Absorption, Distribution, Metabolism and Excretion (ADME) and Toxicology studies from
  • First human dose prediction
  • Synergies between ADME and Toxicology studies during early drug development
  • Early Drug Development Plan – studies and critical milestones
  • Quality standards during Early Drug Development
  • Key regulatory documents & submission of ADME and Toxicology data
Who should Attend

From Pharmaceutical, Biotech, Biologics, Drug Development, Pharmacology, and Drug Manufacturing with job titles such as:

  • Research Scientist / Pre-clinical Scientists
  • Project Managers, Project Coordinators
  • Toxicologists
  • Drug development program managers
  • CMC/Manufacturing Scientists and Managers
  • Outsourcing managers
  • Regulatory Affairs Managers
  • Business Managers
  • Outsourcing strategyCRO selection Study management and monitoring
  • Quality Assurance Professionals

More Details

Prices:
1496-2396 Euro (Estimated)
Organizer:
Fleming
Website:

Future Events

Past Events

Important

Please, check "Toxicology, ADME & Early Drug Development Plan" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma
Science: Biochemistry, Chemistry, Life Sciences & Biology

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