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eCTD Publishing – Fundamentals Training Course

  • 57 Steps
Get a certificate by completing the program.

About

This course provides a clear, practical introduction to eCTD publishing for professionals entering regulatory publishing or transitioning from regulatory affairs, operations, or life sciences roles. The focus is on: - Understanding how eCTD works in practice - Knowing why regulators require it - Building confidence to support or perform publishing activities - This is not academic training. It reflects real-world regulatory publishing workflows used in industry. Learning Outcomes: - By the end of this course, learners will be able to: - Explain what eCTD is and why it is required - Understand the structure of an eCTD submission - Describe lifecycle management and sequences - Recognise common publishing errors - Interpret basic validation results - Understand the role of publishing tools and portals

You can also join this program via the mobile app. Go to the app

Instructors

Price

£550.00

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EMEA
MHRA
FDA
swissmedic
Health CA

Regulatory Submission Services | eCTD Publishing Experts – eCTD Pharma
At eCTD Pharma, we deliver industry-leading regulatory submission services tailored for the pharmaceutical, biotech, and healthcare sectors. Our expertise in eCTD publishing, regulatory gap analysis, and legacy submission conversions ensures your submissions are 100% compliant with EMA, FDA, and global health authority standards. Using advanced Freyr software, we provide fast, accurate, and secure electronic submissions, reducing approval timelines and minimizing compliance risks. Whether you need end-to-end eCTD submission support, lifecycle management, or expert consultancy, eCTD Pharma is your trusted partner. Maximize compliance. Minimize delays. Accelerate approvals. Contact eCTD Pharma today to streamline your regulatory process.

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