🔔 𝗪𝗲𝗹𝗰𝗼𝗺𝗲 𝘁𝗼 𝗼𝘂𝗿 𝗘𝘅𝗰𝗹𝘂𝘀𝗶𝘃𝗲 𝗥𝗧𝗢 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗚𝘂𝗶𝗱𝗲! 🚀 Struggling with RTO validation? You're not alone! In this video, Ben Thakkar, CEO and Senior Consultant at VET Resources, breaks down the entire validation process into simple, actionable steps that will help you ensure compliance with ASQA standards. ✅𝗪𝗵𝗮𝘁'𝘀 𝗜𝗻𝘀𝗶𝗱𝗲? 📋 𝗦𝘁𝗲𝗽-𝗯𝘆-𝘀𝘁𝗲𝗽 𝗴𝘂𝗶𝗱𝗲 to understanding validation requirements under SRTOs 2015. 👥 𝗪𝗵𝗼 𝗰𝗮𝗻 𝗰𝗼𝗻𝗱𝘂𝗰𝘁 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 and how to assemble your team. 📅 𝗖𝗿𝗲𝗮𝘁𝗶𝗻𝗴 𝗮 𝟱-𝘆𝗲𝗮𝗿 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗽𝗹𝗮𝗻 and aligning it with industry best practices. 🛠 𝗣𝗿𝗲𝗽𝗮𝗿𝗶𝗻𝗴 𝗮 𝗰𝗼𝗺𝗽𝗿𝗲𝗵𝗲𝗻𝘀𝗶𝘃𝗲 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗳𝗿𝗮𝗺𝗲𝘄𝗼𝗿𝗸 with all necessary forms and policies. 🔄 𝗜𝗻𝗰𝗹𝘂𝗱𝗶𝗻𝗴 𝗥𝗣𝗟 𝗮𝗻𝗱 𝗿𝗶𝘀𝗸 𝗶𝗻𝗱𝗶𝗰𝗮𝘁𝗼𝗿𝘀 in your validation process. ⏰ 𝗕𝗲𝘀𝘁 𝘁𝗶𝗺𝗲𝘀 𝘁𝗼 𝘀𝗰𝗵𝗲𝗱𝘂𝗹𝗲 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 and how to notify your team. 📊 𝗚𝗮𝘁𝗵𝗲𝗿𝗶𝗻𝗴 𝗮𝗻𝗱 𝗮𝗻𝗮𝗹𝘆𝘀𝗶𝗻𝗴 𝘀𝘁𝘂𝗱𝗲𝗻𝘁 𝗱𝗮𝘁𝗮 to identify areas for improvement. 🔍 𝗖𝗼𝗻𝗱𝘂𝗰𝘁𝗶𝗻𝗴 𝗲𝗳𝗳𝗲𝗰𝘁𝗶𝘃𝗲 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 and retaining all necessary evidence for audits. This guide is packed with 𝗲𝘅𝗽𝗲𝗿𝘁 𝘁𝗶𝗽𝘀 and 𝗶𝗻𝘀𝗶𝗴𝗵𝘁𝘀 that will make RTO validation a breeze! Don’t miss out on these essential strategies to elevate your RTO’s validation process. 👉 𝗛𝗶𝘁 𝘁𝗵𝗲 𝗽𝗹𝗮𝘆 𝗯𝘂𝘁𝘁𝗼𝗻 𝗻𝗼𝘄 𝗮𝗻𝗱 𝘀𝘁𝗮𝗿𝘁 𝗺𝗮𝘀𝘁𝗲𝗿𝗶𝗻𝗴 𝗥𝗧𝗢 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻! 🎥 👍 𝗜𝗳 𝘆𝗼𝘂 𝗳𝗼𝘂𝗻𝗱 𝘁𝗵𝗶𝘀 𝘃𝗶𝗱𝗲𝗼 𝗵𝗲𝗹𝗽𝗳𝘂𝗹, 𝗽𝗹𝗲𝗮𝘀𝗲 𝗹𝗶𝗸𝗲, 𝘀𝗵𝗮𝗿𝗲, 𝗮𝗻𝗱 𝘀𝘂𝗯𝘀𝗰𝗿𝗶𝗯𝗲 𝗳𝗼𝗿 𝗺𝗼𝗿𝗲 𝘃𝗮𝗹𝘂𝗮𝗯𝗹𝗲 𝗰𝗼𝗻𝘁𝗲𝗻𝘁. 🗨️ 𝗛𝗮𝘃𝗲 𝗾𝘂𝗲𝘀𝘁𝗶𝗼𝗻𝘀? 𝗗𝗿𝗼𝗽 𝘁𝗵𝗲𝗺 𝗶𝗻 𝘁𝗵𝗲 𝗰𝗼𝗺𝗺𝗲𝗻𝘁𝘀 𝗯𝗲𝗹𝗼𝘄! 𝗥𝗲𝗹𝗮𝘁𝗲𝗱 𝗥𝗲𝘀𝗼𝘂𝗿𝗰𝗲𝘀: • 𝗥𝗲𝗮𝗱 𝗼𝘂𝗿 𝗱𝗲𝘁𝗮𝗶𝗹𝗲𝗱 𝗯𝗹𝗼𝗴 𝗼𝗻 𝗥𝗧𝗢 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻: https://lnkd.in/g3rVGEs7 • 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗙𝗼𝗿𝗺: [https://lnkd.in/ghYQymSr] • 𝗔𝗰𝗰𝗲𝘀𝘀 𝘁𝗵𝗲 𝟱-𝘆𝗲𝗮𝗿 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 𝗽𝗹𝗮𝗻 𝗱𝗼𝗰𝘂𝗺𝗲𝗻𝘁 : [https://lnkd.in/gt7pPFNf] #RTOValidation #ComplianceMadeEasy #VETResources #ASQAStandards #TrainingAndAssessment #RTOCompliance #ValidationTips #ContinuousImprovement #RTOGuidance #EducationExcellence

Is Automation the Future of OOS Investigations? Weighing the Pros and Cons! In an era where efficiency and accuracy are paramount, many companies are turning to automation for their Out-of-Specification (OOS) investigations. But is this the right move for your team? Let's explore the potential benefits and challenges of automating the OOS investigation process. What's your take? Have you considered automating your OOS investigations? If so, what challenges or successes have you encountered? Let's share our insights and experiences! #OOSInvestigations #AutomationInPharma #Quality Control #PharmaTech #ProcessImprovement

Want to enhance your QA processes? In this on-demand webinar, Giuseppe Grimaldi shares expert tips on tool verification and calibrations, helping you ensure top-tier quality in every step. Watch it today! #AtlasCopco #Webinar #QualityAssurance

Want to enhance your QA processes? In this on-demand webinar, Giuseppe Grimaldi shares expert tips on tool verification and calibrations, helping you ensure top-tier quality in every step. Watch it today! #AtlasCopco #Webinar #QualityAssurance

Want to enhance your QA processes? In this on-demand webinar, Giuseppe Grimaldi shares expert tips on tool verification and calibrations, helping you ensure top-tier quality in every step. Watch it today! #AtlasCopco #Webinar #QualityAssurance

Quality assurance (QA) professionals working in life sciences - your quest for excellence in document reviews is about to get a significant boost! Join us for an enlightening webinar that promises to transform your approach. Harry Hudson will dissect the complexities of document review processes. Whether it’s battling inconsistencies or striving for regulatory approval, this session is designed to address your most pressing concerns. From establishing robust procedures to leveraging technology for transparency, expect plenty of insights and best practices tailored for the life sciences sector. It's your opportunity to refine your processes, expedite approvals and instill a culture of quality. Register now ⬇️ #lifesciences #qualityassurance #documentreview

Quality assurance (QA) professionals working in life sciences - your quest for excellence in document reviews is about to get a significant boost! Join us for an enlightening webinar that promises to transform your approach. Harry Hudson will dissect the complexities of document review processes. Whether it’s battling inconsistencies or striving for regulatory approval, this session is designed to address your most pressing concerns. From establishing robust procedures to leveraging technology for transparency, expect plenty of insights and best practices tailored for the life sciences sector. It's your opportunity to refine your processes, expedite approvals and instill a culture of quality. Register now ⬇️ #lifesciences #qualityassurance #documentreview

Do you know the PDCA cycle ensures that the manufacturers have met the desired quality standards and help them design the quality management framework? Peek into the infographic below to learn the PDCA cycle approach and its benefits. Visit: https://bit.ly/3MbPUe3   #MedicalDevices #QMS #PDCA #qualitymanagement #Infographic #Freyrsolutions #Regulatoryservices #compliance

“Partnering with Veeva and having help with validation plus taking out-of-the-box type functionality allowed us to implement far faster than almost any other product out there.” - Greg Adcock, Senior Director, Quality Systems, Arcellx The quality systems director at Arcellx describes why it was important to invest in a quality management and training system early on to prevent issues down the road to commercialization. Learn why the ease of use and consistency across Vault Training and Vault QualityDocs has Greg getting compliments from his teams. #training #documentmanagement #rolebased #compliance #accountability #transparency https://lnkd.in/gwV68SSd

Quality assurance (QA) professionals working in life sciences - your quest for excellence in document reviews is about to get a significant boost! Join us for an enlightening webinar that promises to transform your approach. Harry Hudson will dissect the complexities of document review processes. Whether it’s battling inconsistencies or striving for regulatory approval, this session is designed to address your most pressing concerns. From establishing robust procedures to leveraging technology for transparency, expect plenty of insights and best practices tailored for the life sciences sector. It's your opportunity to refine your processes, expedite approvals and instill a culture of quality. Register now ⬇️ #lifesciences #qualityassurance #documentreview