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Course topic

  1. Topics
  2. Teaching & Academics
  3. eCTD Submissions

eCTD Submissions

Also indexed asElectronic Submissions · Regulatory Filings · CTD

Learn to prepare and manage Electronic Common Technical Document (eCTD) submissions for efficient global drug registration and approvals.

Courses indexed
5
Live offers
1
Free & coupon courses onlyChange view
Mastering CMC for Biologics: IND to BLA |EMA| FDA | PMDA |
Instructor Seema Singh
Seema Singh
1 course
English
Mastering CMC for Biologics: IND to BLA |EMA| FDA | PMDA |

Mastering CMC for Biologics: IND to BLA |EMA| FDA | PMDA |

(4.50 with 1 reviews)
21
students
6.3 hours
content
Jul 2026
updated
$219.99
Regulatory Affairs US-FDA Electronic Submission Gateway tool
Instructor Mahesh Pratapwar
Mahesh Pratapwar
1 course
English
Regulatory Affairs US-FDA Electronic Submission Gateway tool

Regulatory Affairs US-FDA Electronic Submission Gateway tool

(3.62 with 26 reviews)
1.7K
students
1.1 hours
content
Aug 2025
updated
$14.99
CTD NeeS eCTD compilation & submission of registration files
Instructor Asmaa Khalil El-Kersh
Asmaa Khalil El-Kersh
1 course
Arabic
CTD NeeS eCTD compilation & submission of registration files

CTD NeeS eCTD compilation & submission of registration files

(4.40 with 89 reviews)
1.3K
students
40 minutes
content
Oct 2021
updated
FREE
Certificate Course in Drug Regulatory Affairs (DRA)
Instructor Dr. Sachin Potawale
Dr. Sachin Potawale
1 course
English
Certificate Course in Drug Regulatory Affairs (DRA)

Certificate Course in Drug Regulatory Affairs (DRA)

(4.01 with 2.9K reviews)
11.0K
students
3.1 hours
content
Jun 2026
updated
$17.99
Drug Regulatory Affairs: FDA, EMA, eCTD & Global Compliance
Instructor Dr. Amogh G Nair
Dr. Amogh G Nair
1 course
English
Drug Regulatory Affairs: FDA, EMA, eCTD & Global Compliance

Drug Regulatory Affairs: FDA, EMA, eCTD & Global Compliance

(4.19 with 16 reviews)
549
students
2.4 hours
content
Aug 2025
updated
$14.99

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Topics related to eCTD Submissions

  • 01Drug Regulatory Affairs35
  • 02FDA & EMA Compliance15
  • 03Document Control16
  • 04Good Manufacturing Practices23
  • 05QMS Auditing & Documentation35
  • 06Clinical Trials & Drug Dev49