Clinical Document World

Virtual Conference / Summit
Clinical Trials Pharmaceuticals

Date: 02 to 05 Nov '21
Time: 8:30am to 4:15pm (GMT-08:00) Pacific Time (US and Canada); Tijuana
Price: Under 750 USD$
Special Offer: Use code: industry10 for 10% off

Visit Event Website


At Clinical Document World, our goal is to help you master your clinical documentation skills and strategies. Documentation is involved in just about every aspect of a clinical trial, which is why we strive to give equal focus to key steps of the process - inspection readiness, clinical quality, GCP, and the trial master file.

Learn best practices from industry leaders working at top pharmaceutical companies and contract research organizations. Incorporate new strategies and takeaways from each session into your clinical documentation process, allowing you to improve and maximize the efficiency of your clinical trial. Join us at Clinical Document World this November 2-5, 2021 for a day dedicated to inspection readiness training, followed by 3 full days of educational sessions focused on:

• Document Filing and Improvements
• Trial Master File
• Risk-Based Monitoring
• Inspection Readiness
• Clinical Metrics
• Site - Sponsor - CRO Partnerships
• Clinical Quality
• Documentation Advancements
• Quality by Design
• And many more

Please visit our website to download the full program, view our speaker line-up, or to register.

Remember to use code INDUSTRY10 for 10% off your registration!

Please contact Adriana Murillo at adriana.murillo@gsmiweb.com for questions regarding registration or for group discount inquiries. 

We hope to see you on the virtual event platform!

  • Documentation Management & Processes
  • Quality
  • GCP
  • Inspection Readiness
  • Trial Master File

  • Quality Compliance / Management / Assurance
  • Clinical Documentation
  • Trial Master File
  • Clinical Operations
  • Clinical Trial Management
  • Inspection Readiness team members
  • Trial, Records, Document Management
  • Sites, CROs, & Sponsors
  • Clinical Technology
  • Risk Management
  • GCP


TOP REASONS TO ATTEND INSPECTION READINESS BY CLINICAL DOCUMENT WORLD

 ✔ Interactive educational sessions covering all aspects of clinical document management.

✔  Faculty consisting of professionals from CROs, sites, and sponsors with a diverse background in TMF, quality, technology, and inspections readiness.

✔  Focus on ensuring high quality documentation.

✔  Develop and maintain a culture of inspection readiness.

✔  Utilize new technologies to positively impact your organization’s quality, monitoring, and metrics.

✔  Develop and maintain an inspection readiness management process.

  • Documentation Management & Processes
  • Quality
  • GCP
  • Inspection Readiness
  • Trial Master File

  • Quality Compliance / Management / Assurance
  • Clinical Documentation
  • Trial Master File
  • Clinical Operations
  • Clinical Trial Management
  • Inspection Readiness team members
  • Trial, Records, Document Management
  • Sites, CROs, & Sponsors
  • Clinical Technology
  • Risk Management
  • GCP


TOP REASONS TO ATTEND INSPECTION READINESS BY CLINICAL DOCUMENT WORLD

 ✔ Interactive educational sessions covering all aspects of clinical document management.

✔  Faculty consisting of professionals from CROs, sites, and sponsors with a diverse background in TMF, quality, technology, and inspections readiness.

✔  Focus on ensuring high quality documentation.

✔  Develop and maintain a culture of inspection readiness.

✔  Utilize new technologies to positively impact your organization’s quality, monitoring, and metrics.

✔  Develop and maintain an inspection readiness management process.

Aryn Knight, BS, CCRP

Administrative Director
Texas Heart Institute, Center for Clinical Research

Barbara Novak

Associate Director, Systems & Process Management, Clinical Operations
Kyowa Kirin Pharmaceuticals

Gordon D. Bedford

Regulatory Documentation Specialist
Evelo Biosciences

Karen Roy

Chief Strategy Officer
Phlexglobal

Lisa Mulcahy

Principal Consultant
Mulcahy Consulting, LLC

Sally P. Ton

Senior, eTMF Specialist
Global Blood Therapeutics

Aryn Knight, BS, CCRP

Administrative Director
Texas Heart Institute, Center for Clinical Research

Barbara Novak

Associate Director, Systems & Process Management, Clinical Operations
Kyowa Kirin Pharmaceuticals

Gordon D. Bedford

Regulatory Documentation Specialist
Evelo Biosciences

Karen Roy

Chief Strategy Officer
Phlexglobal

Lisa Mulcahy

Principal Consultant
Mulcahy Consulting, LLC

Sally P. Ton

Senior, eTMF Specialist
Global Blood Therapeutics

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Organizer

Lincoln Health Network

Stay Updated

Organizer

Lincoln Health Network

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