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UPCOMING LIVE SEMINARS
 
Monitoring Clinical Drug Studies: Beginner
August 26-28, 2014
Philadelphia, PA
Clinical Project Management: Advanced
September 10-11, 2014
San Diego, CA






The IND in a CTD/eCTD Format

Upcoming Courses
Course #: BI11770
October 23, 2014
2:30 PM - 4:00 PM Eastern
$695.00

For individual participants, this web seminar qualifies for a reduced individual participant fee of $349. To register, call 1-800-856-2556.

Course #: BI11854
January 22, 2015
12:00 PM - 1:30 PM Eastern
$695.00

For individual participants, this web seminar qualifies for a reduced individual participant fee of $349. To register, call 1-800-856-2556.

Course Description

The Common Technical Document (CTD) format is now the required format for all marketing applications in the U.S., EU, Japan, Canada, and Australia. Clinical Trial Applications (CTAs), the required format of INDs in most countries, are required to be in the CTD format. Currently, the U.S. does not require INDs to be in the CTD format, but rather the traditional format (per regulations in 21 CRF 312.23). However, since all marketing applications are required in the CTD format, it is more efficient to start the IND in the CTD format. If you use the traditional format, the IND and all amendment information must be converted to the CTD format prior to marketing application submission. This conversion time can impact the timeline for marketing application submission, so why not plan ahead for a successful marketing application and start the IND in the CTD format?

Currently, there is no guidance document to facilitate the transfer or mapping of information from the IND requirements contained in 21 CFR 312.23 to the CTD format. There is often a difference of opinion on where information should be stored. This web seminar will give an overview of the IND requirements and where they can most effectively “fit” into the CTD requirements for a streamlined FDA review and building of the IND into a marketing application.

Learning Objectives

  • Describe the Common Technical Document and how and why it came into existence
  • Describe the eCTD and basics tools for eCTD implementation
  • Define a style guide and describe why it is important for eCTD implementation
  • Map the contents of the traditional IND to the CTD format

Who Should Attend

  • Regulatory Affairs Professionals
  • Research and Development Professionals
  • Manufacturing Personnel
  • Clinical Research Professionals
  • Medical Writers

Instructor

Cheryl Vitow

Click here for complete trainer biographies 

Registration Fees

$695

Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.

*For individual participants, this web seminar qualifies for a reduced individual participant fee of $349. To register, call 1-800-856-2556.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will mail ACPE statements within three weeks of program completion.  ACPE#: 0778-0000-14-017-L01-P.  Released: 3/14. 

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.