MedSites Provides regulatory affairs advice at all stages before submission of a dossier for marketing authorization and during the registration process by coming up with the proper response to HAs questions. With our extensive practical experience in regulatory affairs, our experts understand and can interpret regulatory scenarios for clients. We can provide help in seeking the opinion of regulators during the pre-submission phase of a project can prove to be vital; strategies for interacting with regulatory agencies contribute towards achieving consensus at pre-submission meetings. If you need any regulatory advice related to the Egypt countries.