Webinar Highlights:
- Understanding the differences between eCTD 3.2.2 and 4.0.
- Insights from experienced professionals on navigating common challenges.
- Live screening of eCTD 4.0 workflows.
- Interactive Q&A session with our expert panel.
In addition to the webinar, we are excited to announce the launch of the new version of our
NextGen eCTD Software 2.0, which includes advanced features designed to streamline your regulatory submissions. Alongside this, we are also introducing the
PDF Plugin and
Structured Product Labeling (SPL) tools, which will further enhance your document management and submission processes.
Exclusive Launch Highlights:
- NextGen eCTD Software 2.0: Enhanced user interface, improved functionality, and new features for seamless eCTD submissions.
- PDF Plugin: Simplify your document processing for regulatory submission with advanced PDF functionalities.
- SPL Tool: Efficiently manage and submit structured product labeling for US submissions.
Who Attend?
Professionals from the following Departments can Attend:
- Regulatory Affairs
- Regulatory Operations
- Quality Assurance
- Non-Clinical
- Clinical
- Labeling
- QC & Analytical
- Research & Development
- CRO/CMO/CDMO Industry
We look forward to your participation in this informative and engaging event. If you have any questions or need further information, please do not hesitate to contact us at +91 78745 88220/+1 786 448 1648.
