##  [eCTD Ad-Promo Submissions – Compliance Best Practices](/index%2ephp/webinars/ectd-ad-promo-submissions-compliance-best-practices) 

<a>Pharmaceuticals</a>



<a>Past Webinar</a>



## **eCTD Ad-promo Submissions - Compliance Best Practices**

**The webinar was successfully concluded on**

  **June 9, 2021.**

[Download Webinar](javascript:void(0))





We are elated to see your interest in Freyr’s Webinar Series (FWS). The webinar on, “**eCTD Ad-Promo Submissions – Compliance Best Practices,”** was successfully conducted on 9th June 2021. Here is an archived version for your kind perusal.

#### What Was It All About?

In brief, the session, presented by our in-house Regulatory experts – James Hormann aka. Jim Hormann, VP RIMS, focused on:

- Introduction to the guidance and major announcements
- How to fast-track eCTD submissions?
- Major errors to be avoided
- Test submission process

As a continuous practice, Freyr intends to conduct more informative webinar sessions related to the Regulatory aspects of Life Sciences. We presume that you would like to be a part of all our upcoming sessions. If yes, let us have an opportunity to inform you about our next session.