Filing eCTD Submissions Training Course
This intensive one-day course will provide an overview of eCTD submissions and clarify the main components required for a successful submission.
Details
Course overview
The eCTD (electronic Common Technical Document) is now mandatory for submissions in the EU and global regulatory agencies are also moving towards the eCTD as a standard submission process.
This intensive one-day course will provide an overview of eCTD submissions and clarify the main components required for a successful submission. The expert speakers will share their practical experiences of the eCTD and discuss how to implement efficient processes to build and publish submissions in both the EU and US. You will consider the eCTD validation criteria and how to prepare for these in your submissions as well as discuss life cycle management. An interactive case study session will explore eCTD submission challenges and logistics and help consolidate learning.
Benefits of attending:- Clarify the main components of the eCTD
- Learn how to implement efficient processes to build, publish and deliver regulatory eCTD submissions
- Discuss practical experiences of eCTD submissions in the EU and US
- Consider life cycle management for eCTD submissions
Who should attend?
The course will be beneficial to regulatory professionals involved in the preparation of electronic submissions. It will also be of interest to anyone responsible for providing content for the eCTD or who wants to understand the eCTD better.
Programme
Introduction and overview of the eCTD
- The global regulatory framework
The benefits of using MS Word template
- Demonstration of template
What are the main components of the eCTD?
- Metadata
- Documents
- XML backbone
Life cycle management for eCTD submission
- Granularity considerations
- Combining documents
- Use of operators
Review of eCTD validation criteria
- Considerations (inherit zoom, filenames, node extensions etc)
- How to prepare for these (to prevent validation issues)
Practical experiences of submitting eCTDs
- Experiences submitting in EU
- Experiences submitting in US
Live demo
Publish, compile and submit an eCTD sequenceConsiderations for outsourcing
- Why outsource eCTD vs in-house?
- How to select the right eCTD partner
- Best practices for an outsourcing process
Presenters
Marloes van der Geer (More...)
Marloes van der Geer works as senior regulatory affairs scientist at Qdossier. Marloes holds a master in Life Sciences (Drug Innovation) from the University of Utrecht, the Netherlands. For nine years she held several positions at Hoffmann-la Roche in Switzerland, including the role of regulatory intelligence manager and regulatory policy lead for the EMEA region. Marloes has been actively involved in several industry associations like EFPIA and IFPMA. Also, she contributed to the ongoing IMI PREFER project in Europe, focused on the generation and use of patient preference data. In 2019, Marloes joined Qdossier. Marloes’ areas of expertise are: eCTD, lean authoring, publishing, biopharmaceuticals (incl. biosimilars), clinical development, regulatory convergence & harmonization and facilitated registration pathways (incl. orphan drugs), local RA activities (e.g. product information management).
Maikel Bouman (More...)
Maikel Bouman works as a Senior Regulatory Operations Manager at Qdossier and in his role he has a strong focus on managing Regulatory Operations, coordination, and development of staff; planning and coordination of projects, including regulatory filings of dossiers across various regions and development and maintenance of technical solutions supporting Regulatory Operations. Maikel has a broad subject matter expertise on the quality control of data, document publishing, planning/coordination, management, preparation/creation and dispatch of different types of electronic submission formats to various regulatory authorities such as the United States, Canada, Europe, Australia and Switzerland.
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20 Oct 2021 Live webinar |
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20 Oct 2021 Live webinar |
GBP 599.00 EUR 859.00 USD 970.00 + VAT @ 20.00% |
Registration for this event now closed. |
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18 Jan 2022 Face-to-face, (venue not yet confirmed) |
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18 Jan 2022 Face-to-face (venue not yet confirmed) |
GBP 699 599 EUR 979 839 USD 1,090 934 Until 14 Dec* |
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to attend Face-to-face (venue not yet confirmed) |
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25 Apr 2022 Live webinar |
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25 Apr 2022 Live webinar |
GBP 599 499 EUR 859 719 USD 970 814 Until 21 Mar 22* |
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to attend Live webinar |
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11 Jul 2022 Face-to-face, (venue not yet confirmed) |
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11 Jul 2022 Face-to-face (venue not yet confirmed) |
GBP 699 599 EUR 979 839 USD 1,090 934 Until 6 Jun 22* |
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to attend Face-to-face (venue not yet confirmed) |
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19 Oct 2022 Live webinar |
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19 Oct 2022 Live webinar |
GBP 599 499 EUR 859 719 USD 970 814 Until 14 Sep 22* |
Enrol now
to attend Live webinar |
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Learn more about our face-to-face and webinar training formats.
* Note the early booking discount cannot be combined with any other offers or promotional code