Arema

Submission and registration

After a thorough assessment and/or complete preparation of your application, our local agents/partners, present in each country and approved by the authorities, ensure direct submission to the relevant authorities.

They also ensure regular follow-up with the health authorities until the procedure is completed.

Thanks to our tracking platform, you can view the progress of your application and receive clear and detailed updates.

We also assist you in preparing responses to requests for additional information from the authorities, up until the final registration and approval of your product.

After providing you with the appropriate evaluation and/or preparing your dossier, our agents in various countries will submit your file to the respective authorities, follow up your application, and keep you informed.

We also provide you with adequate assistance in responding to authority queries until your product is successfully registered and approved.

Where exactly can we support you?

Need our help?

Contact us for more information.