MRG

𝗬𝗼𝘂𝗿 𝗧𝗿𝘂𝘀𝘁𝗲𝗱 𝗣𝗮𝗿𝘁𝗻𝗲𝗿 𝗶𝗻 𝗠𝗲𝗱𝗶𝗰𝗮𝗹 𝗗𝗲𝘃𝗶𝗰𝗲 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗶𝗼𝗻!  Regulatory approval is the key to getting your medical device to market safely. We offer end-to-end services for seamless SFDA, EDA and MENA region submissions. Let us help you navigate the process with ease and efficiency. #RegulatoryServices #MedicalDeviceIndustry #GlobalCompliance"

The SFDA has officially released a new document detailing inspection and auditing requirements for quality management systems in manufacturers and companies producing medical devices and supplies. A major step forward in maintaining industry safety and regulatory compliance. Reference: https://shorter.me/OwEXn #SFDA #MedicalSupplies #QualityManagement #IndustryStandards

The Egyptian Drug Authority (EDA) has issued new guidelines for submitting files for the first three runs to be analyzed in parallel. A big step towards enhancing efficiency and accelerating the analysis process. Reference: https://shorter.me/SuDzu #EDAUpdates #RegulatoryCompliance #PharmaIndustry

𝗔 𝘀𝘁𝗲𝗽 𝘁𝗼𝘄𝗮𝗿𝗱𝘀 𝘀𝘁𝗿𝗼𝗻𝗴𝗲𝗿 𝗰𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻 𝗶𝗻 𝘁𝗵𝗲 𝗽𝗵𝗮𝗿𝗺𝗮𝗰𝗲𝘂𝘁𝗶𝗰𝗮𝗹 𝘀𝗲𝗰𝘁𝗼𝗿!  The Chairman of the Egyptian Drug Authority met with the Saudi Minister of Industry and Mineral Resources to discuss ways to enhance bilateral cooperation. Their conversation focused on localizing the production of active pharmaceutical ingredients and fostering economic integration between both nations. Together, they aim to achieve shared strategic goals and strengthen their pharmaceutical partnership. Reference: https://shorter.me/dbOL8 #PharmaceuticalPartnership #BilateralCooperation #StrategicGoals #EconomicIntegration

𝗘𝗗𝗔 𝗦𝗲𝗰𝗼𝗻𝗱 𝗘𝗱𝗶𝘁𝗶𝗼𝗻 𝗼𝗳 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗚𝘂𝗶𝗱𝗲 𝗢𝘂𝘁 𝗡𝗼𝘄! The Second Edition of the EDA Regulatory Guide on the registration of Synthetic Peptides that refer to a Reference Peptide Product of rDNA Origin. This updated edition is crucial for those navigating the complex regulatory frameworks of peptide-based therapies. Reference: https://shorter.me/5rZ08 #EDA #RegulatoryUpdates #PeptideTherapies #SyntheticPeptides #rDNAOrigin #PharmaRegulation

𝗘𝘅𝗽𝗲𝗿𝘁 𝗚𝘂𝗶𝗱𝗮𝗻𝗰𝗲 𝗶𝗻 𝗣𝗵𝗮𝗿𝗺𝗮 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲 𝗳𝗼𝗿 𝗙𝗮𝘀𝘁𝗲𝗿 𝗠𝗮𝗿𝗸𝗲𝘁 𝗔𝗰𝗰𝗲𝘀𝘀! In the fast-paced world of pharmaceuticals, staying compliant is key to getting your products to market faster. Our expert regulatory guidance helps you navigate the complexities, ensuring your success from concept to approval. #PharmaCompliance #MarketAccess #RegulatoryExcellence

𝗔 𝗡𝗲𝘄 𝗘𝗿𝗮 𝗼𝗳 𝗘𝗳𝗳𝗶𝗰𝗶𝗲𝗻𝗰𝘆 𝗕𝗲𝗴𝗶𝗻𝘀 𝗪𝗶𝘁𝗵 𝘁𝗵𝗲 𝗘𝗗𝗔!  We’re proud to announce that the EDA Fast Track system is now available for all submissions to the Trademarks and Labeling Evaluation Unit for human pharmaceuticals. This step will accelerate the approval process, ensuring timely delivery of vital treatments. Reference: https://shorter.me/yEHQi #FastTrackSystem #RegulatoryAffairs #Pharma

MRG is heading to CPhI Middle East 2024! Meet us to explore how our pharma regulatory services can help you navigate the regulatory challenges and succeed in the global market. We’re excited to connect with industry leaders and professionals. #CPhI2024 #MRGPharma #PharmaIndustry

Regulatory operations have been upgraded! We’re pleased to announce that starting December 1, 2024, the SFDA’s ePCS and Ghad portal will feature important updates that streamline regulatory procedures, speed up product registration, and ensure adherence to updated guidelines. These improvements are designed to make compliance easier and more efficient than ever before. hashtag #ePCS hashtag #GhadPortal hashtag #RegulatoryUpdates hashtag #Efficiency hashtag #Compliance

Today, we join the nation in celebrating the UAE National Day! At MRG, we are proud to be part of a country that leads with innovation, unity, and vision. Here's to a future filled with even greater success! 🇦🇪 #UAENationalDay #MRG #Innovation #Unity