. Authorized Representative: MRG functions as the authorized representative through
Our scientific office licensed by The Egyptian drug authority (EDA)-license No.1/2022, ensuring compliance and proper liaison with regulatory bodies.
. Product Registration: MRG handles the assembly and submission of comprehensive product
registration files to The Egyptian Drug Authority (EDA) facilitating a smooth approval process.
. Scientific Committee Review: When necessary, MRG submits the required documentation to
the scientific committee for thorough review and approval.
. Change Notifications: MRG promptly notify The Egyptian Drug Authority (EDA) of any
changes or variations in product details or manufacturer information, ensuring ongoing
compliance.
. Post-Marketing and Vigilance: MRG acts on behalf of the manufacturer in managing
post-marketing activities and vigilance, addressing any issues that arise after the product
is on the market.
. Advertising Approvals: MRG ensure that all advertising and promotional activities are
officially approved by the authority The Egyptian Drug Authority (EDA).
. Registration shipments Approvals: MRG obtains the necessary approvals for the release of
samples for registration shipments, ensuring that all products are compliant with regulatory requirements.
. Closing Gaps with Health Authorities: MRG promptly addresses The Egyptian Drug
Authority (EDA) information requests, bridging gaps between regulatory authorities and
manufacturers to ensure compliance and a smooth process.