New Registration
Registration of pharmaceutical products, food supplements, and medical devices in accordance with the relevant national or regional regulatory frameworks.
New drug registration detailsMaintaining market authorization may require updates to approved documentation and regulatory submissions reflecting changes to the registered product.
URAS PV provides ongoing regulatory support to help clients maintain their existing product registrations throughout their lifecycle.
By coordinating these activities with our local regulatory partners, we help clients maintain regulatory compliance and reduce the administrative burden of managing registrations across multiple markets.
Registration of pharmaceutical products, food supplements, and medical devices in accordance with the relevant national or regional regulatory frameworks.
New drug registration detailsMarketing authorization held by the manufacturer, an eligible local entity, a local distributor or another authorized applicant.
Registration models and MAH optionsRenewal of existing marketing authorizations and registration certificates, with ongoing support to maintain your registrations throughout their lifecycle.
Drug license renewal detailsPrice registration, price declarations and reference pricing documentation where pricing approval is required before launch.
Price registration detailsTrademark availability searches, filing and maintenance through local intellectual property specialists.
Trademark registration detailsMAH arrangements, price registration, trademark protection, and an overview of our full registration support.
All registration servicesTell us about your products and target countries, and our regulatory team will outline the registration pathway.
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