Webcast series: Global regulatory requirements for drug device combination products (DDCs) - Overview for the EU, US, China, MENA, Mexico and other LATAM countries
Global regulatory requirements for drug device combination products (DDCs): You will receive a regulatory overview for the EU, the US, China, MENA, Mexico and other LATAM countries, plus you will obtain tips and tricks by (local) experts on how to speed up the approval process.
- Concept: Five weekly live webcasts à 3/2 hours with longtime experienced speakers
- Regions covered: EU, US, China, MENA, Mexico and other LATAM countries
- Your benefits: Possibility to directly interact with the speaker; you will receive a certificate after each session; you are unable to attend one of the sessions? Profit from the recording of each webcast!
| Veranstaltungs-Code | FB24-516862-61076816 |
Bildungsziel der Schulung:
You are keen to know how to speed up the approval process for your drug device combination products (DDCs) in EU and non-EU countries?
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During this new webcast series you will learn about the specific regulatory aspects for product development and lifecycle management of DDCs in the EU, the US, China, MENA, Mexico and other LATAM countries.
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Four (local) experts will share valuable information regarding
- types of combination products/definitions;
- legislative framework;
- quality requirements/documentation;
- post-approval activities;
- submission process;
- how to receive approval faster
with you.
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After the training course you will have gained a better understanding of the additional and differing regulatory requirements and procedures in the different regions.
You will be provided with tips and tricks to help you master the daily challenges of (post-)approval activities more efficiently.
Veranstaltungsort:
weitere Orte/Termine
Kostenlos Info anfordern
