ASPHALION REGTALK | CLINICAL TRIALS INFORMATION SYSTEM

At ASPHALION, we invite you to our second “RegTalk”, one-to-one talks carried out by experts in different areas, aimed at informing about the latest news in the Regulatory Affairs landscape.

At ASPHALION, we invite you to our second “RegTalk”, one-to-one talks carried out by experts in different areas, aimed at informing about the latest news in the Regulatory Affairs landscape.
August 5, 2021

At ASPHALION, we invite you to our second “RegTalk”, one-to-one talks carried out by experts in different areas, aimed at informing about the latest news in the Regulatory Affairs landscape.

In this occasion, we would like to get you acquainted with the Clinical Trials Information System. Our experts, Christopher Mann, PhD, Scientific and Regulatory Affairs Director and Nuria García Pazos, Senior Regulatory Affairs Officer and Project Manager at ASPHALION will provide you with an overview about CTIS, which will be the single entry point for submitting clinical trials information in the EU once it becomes applicable, foreseeable on January 31st, 2022.

We hope the content will be of your interest and you will find it valuable.

Enjoy our RegTalk: “Key factors about the implementation of the new Clinical Trials Information System (CTIS)”

For futher information, you can contact us at:

info@asphalion.com

You can watch the whole RegTalk here:

ASPHALION REGTALK | CLINICAL TRIALS INFORMATION SYSTEM

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