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Klifovet's first webinar series finished successfully

“Regulations and approval processes for veterinary drugs in different regions of the world (EU, AUS, USA, JAP) - An overview”



From October 17th to October 26th, we conducted our first webinar series on the regulatory processes to obtain marketing authorizations for animal drugs. It was a great opportunity to reach many people all across the world without much travelling.


Four one-hour sessions focused on the registration procedure in four different regions: Europe, Australia, the US, and Japan. Each session was held by a regulatory expert from the respective region, all of them partners of Klifovet. Combining the advantages of close contact and coordination between us and the partners with each partner’s local expertise and integration makes it possible for us to act globally for our clients - on the high quality level only a local partner with an established local network can supply.

Each of the sessions gave an overview on
•    The procedures to obtain approval
•    Differences for pharmaceuticals and immunologicals
•    Costs related to the registration procedure
•    Data requirements to obtain approval
•    Regional hot topics

It was interesting how differently all of the covered regions handled the same task: How can it be assured that a veterinary medicinal product has a certain quality and is efficacious and safe for the animal itself, its user, and the environment. Procedures, timelines, and costs to obtain a marketing authorization can differ much, although all four regions have high standards.

More than a hundred sessions were booked, a number that makes us really proud. Thanks to all participants and speakers!