The “Drug Approval Process: Preparation and Processing of INDs and NDAs” seminar will take place from 8 to 9 December in Zurich, Switzerland.

This seminar will present all the requirements to obtain FDA permission to market a Drug product in the USA and will introduce FDA and its laws, regulations, policies and guidelines.

It will be an opportunity to learn about:

• FDA;
• FDA laws, regulation, policies and guidelines;
• the fastest and most cost-efficient way onto the USA marketplace;
• drug development.

More information:

https://www.globalcompliancepanel.com/control/drug-approval-process-drug-development-switzerland-900140-seminar?channel=mailer&camp=webinar&AdGroup=ALBERT_GHINGNONE_DEC08-09_NOV07_PARTA