Schlafender Hase’s Post

I’m happy to share that I have obtained my RAC-Devices certification from the Regulatory Affairs Professionals Society (RAPS) to be listed among the global regulatory professionals who have obtained double RAC designations. I am driven by the desire to offer a one-stop-shop for drug and medical device expertise and to leverage my niche knowledge and skills in combination product development, which has observed a consistent and robust growth. God be praised, the source of my strength! #Continuouslearning #NextGenregulatoryprofessional #Drugdevelopment #Medicaldevicedevelopment #Combinationproductdevelopment #Globalregulatorystrategy

I am thrilled to announce that I have successfully completed the eCTD submissions course through the Global Institute of Regulatory Affairs! This achievement has equipped me with the necessary knowledge and skills to navigate the intricacies of regulatory affairs. I am eager to apply this expertise to my work and contribute to the success of my organization. A big thank you to the Global Institute of Regulatory Affairs for providing me with this valuable opportunity to enhance my professional development! #GlobalInstituteofRegulatoryAffairs #ProfessionalDevelopment #RegulatoryAffairs #eCTD #ContinuingEducation

Mastering the Basics: Introduction to Common Technical Document (CTD) for Regulatory Submissions https://lnkd.in/dGtJ4DqK #MasteringTheBasics #CTD #RegulatorySubmissions #TechnicalDocuments #PharmaSubmissions #DrugRegulations #ClinicalSubmissions #CTDFormat #HealthcareCompliance #PharmaRegulatory #RegulatoryAffairs #DrugApproval #RegulatoryScience #CTDBasics #PharmaceuticalIndustry #RegulatoryGuidelines #CTDSubmission #TechnicalWriting #HealthcareRegulations #CTDTraining #RegulatoryCompliance

🌟 Exciting News! 🚀✨ I am thrilled to share that I have officially become a member of the Regulatory Affairs Professionals Society (RAPS). 🎉🧬💡 This marks an important milestone in my journey as a regulatory professional, and I look forward to engaging with a global community of experts and leaders in the field of regulatory affairs. Joining RAPS is not just about professional development, but also about staying at the forefront of industry trends, advancing regulatory science, and contributing to the development of global health standards.🌍📊 #RAPS #RegulatoryAffairs #ProfessionalGrowth #Pharmacy #Biotechnology #RegulatoryScience #HealthcareInnovation #LifelongLearning

"Excited to share that I've completed the Certificate Course in Regulatory Affairs from IMSR! 🎓💼 This journey has been enlightening, exploring the nuances of regulatory compliance in the industry. I'm eager to utilize this knowledge to uphold product quality and compliance standards. #RegulatoryAffairs #ContinuousLearning #IMSR"

Mastering the Basics: Introduction to Common Technical Document (CTD) for Regulatory Submissions https://lnkd.in/dh9MTcCR #CTD #CommonTechnicalDocument #RegulatorySubmissions #PharmaRegulations #MasteringCTD #DrugApproval #PharmaceuticalIndustry #CTDFormat #RegulatoryCompliance #HealthcareRegulations #CTDBasics #RegulatoryAffairs #ClinicalSubmissions #HealthcareCompliance #DrugDevelopment #PharmaSubmissions #PharmaceuticalRegulations #CTDSubmission #TechnicalDocuments #RegulatoryGuidelines #PharmaceuticalCompliance #HealthcareIndustry #DrugSafety #RegulatoryScience #PharmaRegulatory #ClinicalResearch #DrugEvaluation #CTDStructure #ClinicalTrials #RegulatoryRequirements #HealthcareLaw #PharmaceuticalStandards #DrugApprovalProcess #GlobalRegulations #PharmaDocumentation #CTDImplementation #PharmaGuidelines #RegulatoryFramework #RegulatoryProcesses #ClinicalDevelopment #RegulatoryManagement #PharmaStrategy #HealthcareStandards #QualityManagement #DrugRegulation #RegulatoryDocumentation #PharmaCompliance #HealthcareDocuments #RegulatoryProcedures #CTDPreparation #PharmaLaws

Get a first impression of how Elly "Your Personal Regulatory Affairs Assistant" works in the video below. Lern more under: www.regulationagent.com #regulatoryaffairs #medicaldevice #mdr #ivdr

Mastering the Basics: Introduction to Common Technical Document (CTD) for Regulatory Submissions https://lnkd.in/dh9MTcCR #CTD #CommonTechnicalDocument #RegulatorySubmissions #PharmaRegulations #MasteringCTD #DrugApproval #PharmaceuticalIndustry #CTDFormat #RegulatoryCompliance #HealthcareRegulations #CTDBasics #RegulatoryAffairs #ClinicalSubmissions #HealthcareCompliance #DrugDevelopment #PharmaSubmissions #PharmaceuticalRegulations #CTDSubmission #TechnicalDocuments #RegulatoryGuidelines #PharmaceuticalCompliance #HealthcareIndustry #DrugSafety #RegulatoryScience #PharmaRegulatory #ClinicalResearch #DrugEvaluation #CTDStructure #ClinicalTrials #RegulatoryRequirements #HealthcareLaw

Mastering the Basics: Introduction to Common Technical Document (CTD) for Regulatory Submissions #MasteringTheBasics #CTD #RegulatorySubmissions #TechnicalDocuments #PharmaSubmissions #DrugRegulations #ClinicalSubmissions #CTDFormat #HealthcareCompliance #PharmaRegulatory #RegulatoryAffairs #DrugApproval #RegulatoryScience #CTDBasics #PharmaceuticalIndustry #RegulatoryGuidelines #CTDSubmission #TechnicalWriting #HealthcareRegulations #CTDTraining #RegulatoryCompliance

🎙 𝐖𝐡𝐚𝐭 𝐢𝐬 𝐭𝐡𝐞 𝐛𝐞𝐬𝐭 𝐐𝐮𝐚𝐥𝐢𝐭𝐲 & 𝐑𝐞𝐠𝐮𝐥𝐚𝐭𝐨𝐫𝐲 𝐀𝐟𝐟𝐚𝐢𝐫𝐬 𝐌𝐢𝐧𝐝𝐬𝐞𝐭? 🎙 Michelle Lott, RAC, and Monir El Azzouzi are discussing their Experience in the Quality and Regulatory affairs area. They will help you define what is compliance and how they think it should be applied. Michelle had also some good and bad experiences that she is sharing with us. 📢 Don't miss out on this opportunity to gain practical wisdom and guidance from seasoned experts in the field! 🔍 Curious to know? Watch the discussion here: https://lnkd.in/eutgi-Ar