eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada

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2-Day In-Person Seminar, from COMPLIANCE TRAININGS (Code – SEM9017)

eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada

PEGGY J BERRY

Synergy Consulting

March 8 – 9, 2018

Philadelphia, PA, USA

 

Why You Should AttendAgendaSpeakerPricingVenue
The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD – Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times.

This two day workshop will provide you with an in-depth review of the content and format requirements of the CTD/eCTD. Hands-on activities will include organizing specific study reports and other documents into the CTD, using tools for the project management of the CTD preparation, and pre-publishing an eCTD. .


Who Should Attend :

  • Regulatory Affairs Departments
  • Quality Assurance Departments
  • Regulatory professionals
  • Pharmacovigilance Professionals
  • Project Management
  • Regulatory Operations Departments
  • Medical and Technical writers
  • Professionals preparing IND, DMFs, NDAs and other submissions
  • IT Professionals
  • Everyone responsible for providing content for the CTD
Seminar Fee Includes:
Training
Lunch
AM-PM Tea/Coffee
Seminar Materials
USB with Presentation Handout
Attendance Certificate
Networking Sessions
$100 Gift Voucher for next seminar

DAY 1 (8:30 AM – 4:30 PM):

Registration Process – (8:30 AM – 9:00 AM)

  • Lecture 1 – Overview of the drug development program and source of relevant submission documents
  • Lecture 2 – Discussion of the roles and responsibilities for CTD preparation
  • Lecture 3 – Review of the CTD format requirements
  • Lecture 4 – Discussion on the successful transition from other formats to the CTD
  • Lecture 5 – Placement of content into the CTD format; including less obvious items
  • Lecture 6 – Review of different requirements across regions (US, EU, Canada)
  • Lecture 7 – Implementing tools for the project management of CTD preparation and publishing

DAY 2 (8:30 AM – 4:30 PM):

 

  • Lecture 8 – Technical requirements for an eCTD submission
  • Lecture 9 – Document naming requirements
  • Lecture 10 – Building the folder structure
  • Lecture 11 – Internal document requirements for the eCTD
  • Lecture 12 – Performing “pre-publishing” work for each document
  • Lecture 13 – Tools for tracking and managing eCTD content
  • Lecture 14 – Performing quality checks on the eCTD
  • Lecture 15 – Updating content in the CTD and eCTD (amendments, supplements, variations, etc.)

Peggy J. Berry

President & CEO at Synergy Consulting


Peggy J. Berry, MBA, RAC, is the President & CEO at Synergy Consulting where she provides consulting services to companies in all aspects of drug development. She also provides group and one-on-one training in drug development, regulatory affairs and project management topics. Prior to founding Synergy Consulting in 2015, she was Vice President of Regulatory Affairs at Insmed (2/2015-5/2015) where she was responsible for the development and implementation of global regulatory strategies and the management and oversight of the regulatory affairs department. Prior to Insmed, she was Vice President of Regulatory Affairs and Quality at Amarin (3/2009-2/2014).

She has also held a variety of senior level positions at Dyax (5/2006-3/2009), MGI Pharma (now Eisai; 7/2005-5/2006), AstraZeneca (10/2001-7/2005), and Dey Pharma (now Mylan; 12/1997-10/2001). She has also held Regulatory Affairs roles within two clinical contract research organizations (ILEX Oncology and Cato Research Ltd; 1992-1997) and has worked in review divisions at the FDA (1985-1992). In addition, Ms. Berry consults for a number of companies in the regulatory and quality area, conducts a number of training courses, and is active in the Regulatory Affairs Professionals Society. She is the editor of the 2010 book “Choosing the Right Regulatory Career” (RAPS, MD) and author of the 2011 book “Communication & Negotiation” (RAPS, MD).

 

PRICING OPTIONS
For Single Delegate – $ 1400 (Save $ 200 on Early Bird Discount)
Regular Price – $ 1600

Group of 3 Delegates – Get 10% Discount (Save $ 1020)
Group of 5 Delegates – Get 20% Discount (Save $ 2400)

EARLY BIRD OFFERS CLOSES ON FEBRUARY 23, 2018
 
 
 
 
Early bird seats are limited and based on first-come, first-serve..(Only 5 Remaining)
 

For discounts on multiple registrations, contact customer care at +1-416-915-4458

 
REGISTER NOW


Payment Options

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  • Make Secure Payment using Credit Card
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  • Click on Proceed to Checkout on the Cart Page, and complete the registration.
  • Once the payment is completed, you will be receiving a Form to fill up the Delegates Information
  • An electronic event pass (eTicket) will be sent to the email addresses associated with the registered delegates, 5 working days before the seminar date.
  • Please bring the respective passes to the event venue.


Pay by Wire:

  • Please contact our support to assist you with registration by Wire
  • Support Number: +1-416-915-4458
  • E-mail: info@webinarcompliance.com

By Check:

  • Pay your check to (payee name) “FutureCorp Consulting Inc” our parent company
  • Please send the Scanned copy of the check to info@webinarcompliance.com
  • Mail the check to:
    FutureCorp Consulting Inc
    5969, Candlebrook Ct.,
    Mississauga, ON L5V 2V5,
    Canada
  • Once we receive the check, you will be receiving a Form to fill up the Delegates Information
  • After payment receipt, from the registered attendee, an electronic event pass (eTicket) will be sent to the email addresses associated with the registered delegates, 5 working days before the seminar date. Please bring the respective passes to the event venue.
 

Philadelphia, VA, USA

(Venue to be announced shortly)
March 8 – 9, 2018
 
  

Call for Assistance: +1-416-915-4458

  

REGISTER NOW