5th Clinical Regulatory Medical Writing Forum – 5th Clinical Regulatory Medical Writing Forum

Medical writers have the task of accurately understanding and summarizing complex information that ranges from scientific data in molecular biology and pharmacokinetics to statistical analysis plans and clinical outcomes. This data needs to be effectively shared in well-written, legible and compliant documents. Medical writers are also tasked with coordinating with internal stakeholders to get documents approved on time while receiving contributions from the right people. Because these documents are evaluated by regulatory agencies, it is vital for medical writers to stay up to date with the latest regulatory developments and anticipate how their documentation processes might be impacted.

The 5th Clinical Regulatory Medical Writing Forum is designed to provide attendees with the strategies and insights needed to efficiently compose clinical regulatory documents, manage in-house and external resources, effectively execute the writing process, and understand the recent developments in regulations.

Featured Speakers

Top Five Reasons to Attend

  • Gain valuable insight on the impact of transparency requirements and implementing EMA Policy 0070 in medical writing
  • Discover which tools and technologies can help expedite the medical writing process
  • Analyze the benefits of having a medical writer as a strategic partner in document preparation and submission planning
  • Create models for working with vendors/contractors that can adapt to changing program and document needs
  • Develop effective onboarding and mentoring programs that will allow you to recruit millennials and train the next generation of medical writers

Who Should Attend

This conference is of interest to professionals from pharmaceutical, biotechnology and medical device companies who are involved in regulatory medical writing with the following job functions:

  • Medical Writing
  • Regulatory Writing
  • Regulatory Affairs
  • Regulatory Operations
  • Clinical Operations
  • Technical Writing
  • Clinical Research
  • Electronic Submissions
  • Medical Affairs
  • Clinical Documentation
  • Clinical Publishing
  • Submissions and Documentation
  • Global Medical Publishing

This conference is also of interest to:

  • Document Application Suppliers
  • Information Management Consultants
  • Research Informatics
  • Clinical Research Organizations
  • Component Authoring Software Suppliers
  • Publication Service Providers
  • Medical Writing Service Providers
  • Bibliographic Software Suppliers
  • eCTD Suppliers
  • Regulatory Submissions Providers
  • Consultants
  • Structured Content Software Suppliers
Startdate: 2018-07-10
End Date 2018-07-11

Description: The 5th Clinical Regulatory Medical Writing Forum is the premier industry event dedicated to addressing the challenges of clinical and regulatory medical writing professionals.
Performer: ExL Events
Address : 5th Clinical Regulatory Medical Writing Forum