Technical and Regulatory Writing for FDA Regulated Industries 2015

  • 09-10 Jul 2015
  • Dallas, TX, United States

Description

Technical and Regulatory Writing for FDA Regulated Industries 2015 is a course that covers topics such as:

  • How to edit, format, present and publish technical regulatory documents for most favorable reception by regulatory agencies
  • Practical tips using examples on how to organize and deliver information in clear and readable documents
  • Technical, practical, logical and logistical tips for all regulatory writers
  • Rules for writing documents intended for electronic submission to regulatory agencies

Technical and Regulatory Writing for FDA Regulated Industries 2015 brings together:

  • Medical and technical writers
  • Regulatory affairs professionals preparing IND, DMFs, NDAs and other submissions
  • Supervisors and lead workers in regulatory affairs
  • Project managers and directors
  • IT professionals looking to make eCTD submissions
  • Quality assurance and quality control

Past Events

Important

Please, check "Technical and Regulatory Writing for FDA Regulated Industries" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Pharma
Science: Life Sciences & Biology

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