Regulatory

In the complex and highly regulated pharmaceutical industry, compliance with regulatory requirements is of utmost importance. The Regulatory Affairs Department at Evora Associates is dedicated to navigating the intricate landscape of regulatory compliance, ensuring that our clients meet all necessary regulatory standards and guidelines.

Unlocking Opportunities, Enabling Success

EVORA ASSOCIATES

Registering your products with expert advice

Get the best support in registering your products on time and following the local practices that apply for each market

Our Team

Our Regulatory Affairs team comprises experienced professionals who possess in-depth knowledge of local, regional, and international regulatory frameworks. With expertise across a wide range of therapeutic areas and product types, our team is international to guide our clients through the complex regulatory processes.

We can assist you in gaining regulatory approvals. Our team of experts have vast regulatory experience in the following areas of regulatory:

MENA registrations & renewals
DCP registrations & renewals
Asia registration & renewals
LATAM registrations & renewals
Dossier analysis
MA variations
CPP applications
Working with MoH's

Office:

Evora Associates Limited
1st Floor, Gallery Court
Arcadia Avenue
London
N3 2FG
UK

Phone: 0044 7815 146188

Email: businessdevelopment@evora.associates

Privacy Statement

Evora Associates respects the privacy of the visitors to this website. The information that is gathered during the use of this website will only be used for the purposes indicated and in accordance with applicable law. Evora Associates will not give any information to third parties without the explicit permission of the visitor. Furthermore, Evora Associated strive to secure visitor information in such a manner that third parties cannot access this information. While great care is taken to prevent third party access, Evora Associates cannot be held responsible if information is obtained illegally by third parties.