Manal Ayyash’s Post

I’m thrilled to share that I have successfully completed the Drug Regulatory Affairs certification from Pharma State Academy! This journey has deepened my understanding of the regulatory landscape and equipped me with the skills to navigate the complexities of drug development and approval processes. 🌍💊 #DrugRegulatoryAffairs #PharmaStateAcademy #LifelongLearning #HealthcareInnovation

Finished the Drug Regulatory Affairs course with new skills and knowledge, feeling accomplished.

Cliniminds offers Advanced Post Graduate Diploma in Drug Regulatory Affairs, IPR & Patents with placement Support Program inclusion: Certificate Course Hands on eCTD Software Training Free add on Pharmacovigilance Course BATCH COMMENCEMENT: 12th January 2025 (Sunday) DURATION: 6 Months Live eLearning (Weekend) Call/ whatsapp: +91 9310485979 This video focuses on the Regulatory framework in the European Union and the different registration routes followed by the European Medicines Agency (EMA). Watch video: https://lnkd.in/gEDuaYmM #EMA #EU #Regulatory #QA #QC #QCMICRO #pharmaceuticalindustry #Cliniminds #RegulatoryAffairs #RA #Drugregulatoryaffairs #DRA #PharmaRegulations #PharmaceuticalIndustry #RegulatoryCompliance #ClinicalTrials #PharmaRegulatory #DrugApproval #HealthcareCompliance #RegulatoryUpdates #PharmaExperts #PharmacologicalRegulation #GlobalRegulatoryAffairs #DrugDevelopment #PharmaCompliance #HealthcareRegulations #RegulatoryScience #RegulatoryStrategy #PharmaProfessionals #MedicalDeviceRegulations #USRegulations #EURegulations #Regulatoryframework

Hello Connections, Excited to share that I've completed Certificate Course on Drug Regulatory Affairs. It helps to deepen my skills in Drug Regulatory Affairs. I would like thank to Dr. Sachin Potawale for the invaluable knowledge. #RegulatoryAffairs #DrugRegulatoryAffairs #RegulatoryGuidelines

Free demo class on 3 months certificate course in Drug Regulatory Affairs.

Practical Aspects anf Industry Insight of Drug Regulatory Affairs

Drug Regulatory Affairs, IPR & Patents New Batch Date : 15th December 2024 Admission Helpline : +91 93104 85979 #Drug RegulatoryAffairs # PharmaRegulations # PharmaceuticalIndustry # RegulatoryCompliance # FDAApproval # ClinicalTrials # PharmaRegulatory # RegulatoryAffairs # DrugApproval # HealthcareCompliance # RegulatoryUpdates # PharmaExperts # PharmacologicalRegulation # GlobalRegulatory Affairs # DrugDevelopment # PharmaCompliance # HealthcareRegulations # RegulatoryScience # RegulatoryStrategy # PharmaProfessionals # MedicalDeviceRegulations 

successfully completed the certificate course in Drug Regulatory Affairs.

Drug Regulatory Affairs, IPR & Patents Admission Helpline : +91 93104 85979 Batch Date : 1st December 2024 #Drug RegulatoryAffairs # PharmaRegulations # PharmaceuticalIndustry # RegulatoryCompliance # FDAApproval # ClinicalTrials # PharmaRegulatory # RegulatoryAffairs # DrugApproval # HealthcareCompliance # Regulatory Updates # PharmaExperts # PharmacologicalRegulation # GlobalRegulatory Affairs # DrugDevelopment # PharmaCompliance # HealthcareRegulations # RegulatoryScience # RegulatoryStrategy # PharmaProfessionals # Medical DeviceRegulations 

Dear Regulatory Affairs professionals, do you agree that continuously monitoring global regulatory authorities for updates to guidelines, regulations and policies related to drug development, approval processes, labeling and pharmacovigilance is too time-consuming? In our webinar "AI-Powered Regulatory Intelligence in Pharma", please click here to register https://lnkd.in/ePctX9Sd we show how Regulatory Intelligence teams can be freed from this work and at the same time reduce compliance risks. Based on our knowledge and conversation with our customers, we have created a solution that allows the Regulatory Intelligence Manager to be informed more quickly about changes in areas relevant to them without the hassle of manual information collection and assessment. Automated and comprehensive analysis of all regulatory publications, such as EMA or FDA, as well as company and product specific relevance determination for the company, frees up time for more important tasks such as incorporating regulatory information into clinical trial planning, marketing strategies and lifecycle management plans. The main goal here is to shorten the submission process to achieve Marketing Authorization as quickly as possible. Don’t miss the opportunity to get new Insights regarding digitalization in Regulatory Affairs. See you there. #inconsult #regulatoryaffairs #regulatoryintelligence #artificialintelligence