eCTD Submissions of IND and NDA/BLA to the US FDA: Hands-on Workshop

Recording will be available after live training

Date

August 20. 2026

Duration

60 Minutes

Time

10:00 AM – 4:15 PM EST

FDA now requires all DMFs be submitted only in the electronic CTD format which creates a huge burden on owners of most submissions. Converting to eCTD format requires special skills, software and resources, the cost of which could be prohibitive to small manufacturers. Our speaker, Dr. Mukesh Kumar, in this workshop will go over the details of the latest guidance on eCTD submission and explain the key takeaways.

Soon FDA will stop accepting paper submissions of all kinds of applications. Despite there being extensive information available from FDA and other regulatory bodies regarding eCTD submission, creating one and submitting it through the electronic submission gateway (ESG) of the FDA, is a daunting task even for those proficient in computer systems and coding languages. The off-the-shelf software and consultations available are prohibitively expensive not only in the capital investment required but also in terms of the time needed for getting a submission ready.

This one-day workshop is designed to address all these and provide the attendees with step-by-step instructions in creating and submitting eCTD submissions for IND, NDA, BLA, and ANDA applications without the need for expensive tools or unreasonable efforts. This no-frills workshop aims to train in the minimum skills needed and provide hands-on practical tips to create eCTD submissions. The trainers will use their own case studies of how eCTD submissions were created and successfully submitted to the FDA using indigenous tools, eCTD software and expertise. Also discussed will be logistical issues associated with managing and maintaining eCTD compliance with regards to all electronic regulatory submissions. This workshop will be beneficial to both the novices and experienced in the field.

 

Who Will Benefit:

  • Regulatory affairs professionals preparing IND, DMFs, NDAs and other submissions
  • Medical and Technical writers
  • Project Managers, Directors
  • Supervisors, and lead workers in Regulatory Affairs
  • Quality Assurance and Quality Control
  • IT professionals looking to make eCTD publishing and submissions

Speaker: Mukesh Kumar

​PhD, RAC | CEO, FDAMap

For more info, fill the box below. We will contact you within 24 hrs.

Register Online

(By clicking on the links below)

Prices are in US Dollars.

The registration fee includes the workshop and all related course materials.

Terms & Conditions to register for the Workshop

Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this seminar, please email us at info@fdamap.com

Payment:
We accept credit card, debit card, and PayPal.

Cancellations and Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 10 working days prior to the start date of the event will receive a refund — less a $200 administration fee per person. No cancellations will be accepted — nor refunds issued — within 10 working days from the start date of the event.

On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($200) will be transferred to any future FDA Map event and a credit note will be issued.

For more info, fill the box below. We will contact you within 24 hrs.