Mendura Academic Innovators https://validator.w3.org/feed/docs/rss2.html Regulatory Affairs Training Gallery Training Programmes MailPoet Page Home Page RA_Final Assessment What must a company obtain from MOHAP if changes have been made to the product’s packaging or formulation? When should the product renewal process ideally be initiated? What is the primary role of the regulatory committee in the product withdrawal process? In case of variation rejection, what should the Regulatory Officer do first? What is the correct order of review for updated artwork and leaflet translations? What is the waiting period for implementing a Type I B variation after notifying MOHAP? Which of the following is an example of a Type II A Variation? Which type of variation in UAE requires only a notification and does not need prior approval? What is the maximum time allowed to implement an approved variation after receiving the certificate in UAE? What is the final step before the issuance of the registration certificate? During the Quality Control (QC) Sub-Process, which of the following might be requested by MOHAP? Which document is specifically required during the registration of herbal products? Which document is NOT part of the Quality Control (QC) Approval requirements? Which of the following is required for successful e-CTD submission if the principal company lacks GCC license? What is the first step once a drug store receives a complete registration dossier from the MAH? What action must be taken if the registration dossier received from the MAH is incomplete? What is the main objective of product registration with MOHAP? Sensation and Perception II What is the validity of site registration once approved? Which document is mandatory only for conventional medicine site registration? RA_6: GSL, Herbal, and Medical Device Registration What is the validity period of MAH registration in the UAE? Which of the following is NOT a required document for MAH registration? RA_5: Conventional Medical Registration When can the MAH registration application be submitted to MOHAP? In which situation can a product receive direct clearance without full registration? What is the typical duration for MOHAP to complete the product classification process? RA_4: Product Registration Which of the following documents is NOT required for a standard product classification submission? RA_3: MAH & Site Registration in Regulatory Affairs RA_2: Product Classification in Regulatory Affairs RA_9: Product Renewal RA_8: Product Withdrawal RA_7: Overview of Variations in UAE Regulatory Affairs RA_1:Introduction to Regulatory Affairs A Beginner Crash Course Guide What certification must be provided to MOHAP during the site registration of a manufacturing facility? Which of the following is NOT a requirement for MAH registration under MOHAP? Which entity is primarily responsible for obtaining marketing approval for a medical product in the UAE? Which of the following products is most likely to fall under the GSL (General Sale List) category in the UAE? What is the first and most essential step in the medical product registration process under MOHAP in the UAE? mega-item-19688 The final step required to convert vibrations into sound sensations takes place in which part of the ear? Blog