ResearchManager

During our visit to Medica 2024, we explored the latest medical technologies and digital innovations shaping the future of clinical research. From solutions accelerating processes to enhancing collaboration and prioritizing patient-centered approaches, the possibilities are inspiring. These trends reaffirm our mission: creating smart tools like ePRO and eTMF to streamline clinical research and drive impactful progress in healthcare. #Medica2024 #ResearchManager #MedTech #Innovation #ClinicalResearch

📂 How Erasmus MC's Medical Ethics Review Committee reduced double work with ResearchManager RIMS Moving away from USB drives and manual data entry, the Medical Ethics Review Committee (METC) at Erasmus MC now handles submissions, approvals, and document management all in one place. This transition has not only minimized double work but has also provided researchers with an efficient, secure way to stay updated on their projects. Curious about how a digital RIMS platform could work for your Ethics Committee? 🔗 Read the full story here: https://lnkd.in/eedFQVFy #ResearchManager #RIMS #MedicalEthics #IRB #ResearchManagement #DigitalSolutions #METC #ClinicalResearch #ErasmusMC

✅Clean Data Labs Stays Compliant with ResearchManager Clean Data Labs, a Poland-based clinical data management and biostatistics service, needed a GDPR-compliant EDC solution to support their work with partners across Europe and North America. After facing compliance challenges with previous systems, they found their ideal match with ResearchManager. Curious about how ResearchManager helped Clean Data Labs overcome their challenges? 👉 Read more: https://lnkd.in/eq_v87_X #ClinicalTrials #DataManagement #ResearchManager #Compliance #GDPR #Biostatistics #ClinicalData

🚀 Start-up and mid-sized CROs, take note! For CROs looking to make a professional impression on sponsors, the cost of a CTMS or eTMF can be a challenge when funding isn’t yet secured. What if there’s a way to overcome this? Our latest blog compares: ✅ The traditional approach: waiting for the green light ✅ The innovative CTMS and eTMF on demand pricing model Explore the pros and cons of both approaches and see if a CTMS or eTMF on demand could be a breakthrough solution for start-up and mid-sized CROs. 👇 https://lnkd.in/ex63wVYc #CRO #CTMS #eTMF #OnDemand #ClinicalResearch #PricingModel #ClinicalTrialManagement #StudyStartup #DigitalSolutions #InnovativeApproach #LifeSciences #ClinicalData #DrugDevelopment #HealthTech #ClinicalStudy #ResearchEfficiency #SaaS #MidSizedCRO #StartUpCRO #RegulatoryCompliance #StudyManagement #ClinicalOperations #EDC #TechnologyInResearch

🔬 Real World Evidence (RWE) is exactly the innovation healthcare needs. In theory... …but there are pros and cons to using real-world data from patient records, insurance claims, and health apps. We wrote a blog about it, where we explore how the balance tips at the moment. 💡 Real World Evidence (RWE): Should you act now or can it wait? » Read it in our blog: https://lnkd.in/eTVBMSfC #clinicalresearch #RealWorldEvidence #innovation

🔍 Launching a study months earlier? Instituut Verbeeten achieved this with their new CTMS. Everything was well-organized in folders on a hard drive. But sometimes, radiation oncologists at Instituut Verbeeten spent too long searching for the right documents and progress information. The Clinical Trial Management System (CTMS) from ResearchManager changed all of that. Challenges faced by Instituut Verbeeten: 😥 Physicians regularly needed help finding documents 😥 Time-consuming back-and-forth emails caused delays 😥 No clear overview of study progress Results thanks to the CTMS: ✔️ All documents are in one central location ✔️ Fewer questions and more clarity ✔️ All stakeholders have real-time insight into study progress ✔️ Easy data exchange with partners through single sign-on Jorine Vermaire, Research Coordinator at Instituut Verbeeten, says: "The CTMS streamlines the research process, allowing us to launch studies months earlier and help patients sooner." Want to learn more about how the CTMS improved the process at Instituut Verbeeten? Read the full case study: https://lnkd.in/gxH5YvAg #CancerResearch #Healthcare #ClinicalTrials #InstituutVerbeeten #ClinicalResearch #CTMS #MedicalResearch #ResearchTechnology #ClinicalDataManagement #PatientCare #OncologyResearch #ResearchInnovation #HealthcareSolutions #StudyManagement

3 common doubts and objections research teams have about using an ePRO System (even though response rates are 20% higher) 👉 Doubt 1: Will the email with the questionnaire actually reach participants? ✅ Yes, and you can track it in the system. 👉 Doubt 2: What if participants forget to fill out the questionnaire? ✅ The ePRO system sends automatic reminders. 👉 Doubt 3: Are participants really the ones completing the questionnaire? ✅ With IP checks and validation methods, we ensure they are. Most doubts and objections stem from a lack of understanding of how an ePRO system works. And that’s understandable, as many of the processes ensuring study validity happen behind the scenes. That’s why we wrote an article to explain how it all works: https://lnkd.in/gK8CajU8 #ePRO #ClinicalResearch #ClinicalTrials #ResearchTechnology #PatientEngagement #DigitalHealth #ClinicalDataManagement #DecentralizedTrials #HybridTrials #DataAccuracy #ClinicalTrialManagement #ElectronicDataCapture #ClinicalTrialSoftware #PatientReportedOutcomes #Compliance #ClinicalInnovation #RemoteDataCollection #HealthTech #MedicalResearch

Are you allowed to recruit participants 100% digitally for your clinical trial❔ Among our international clientele, we observe significant differences in local laws and regulations. ✔️ In some countries, you are allowed to recruit and guide patients digitally. A digital signature on the patient informed consent form is sufficient. ⛔ In other countries, patients are required to come to the hospital and physically sign before they are allowed to participate. What do you think... …should clinical trials be made more accessible to a broader audience? For instance, you could replace unnecessary hospital visits with a remote appointment, allowing people who live further from hospitals to participate. #clinicaltrials #digitalization

💡 Yes, a digital EDC system costs money. But it also saves money. Research institutions, academic organizations, and CROs often find themselves in doubt: should they invest in an EDC system or not? According to research by Chakraborty et al. (2022), many experience barriers that prevent the adoption of Electronic Data Capture systems. The most cited reasons? Costs and anticipated technical support. But it’s intriguing that they stumble over the initial investment. The same research also delivers good news: By using an EDC system, cost savings of 49 to 62% can be achieved in clinical research. Those are impressive numbers. In short: it’s time for a blog explaining how an EDC system becomes a self-repaying investment in clinical trials. Learn more here: https://lnkd.in/epcBVKnW #EDC #ClinicalResearch #ElectronicDataCapture #CostSaving #ClinicalDataManagement #CRO #ResearchInstitutions #EDCSystem #ClinicalTrials #HealthTech #DataAccuracy #ClinicalInnovation #DigitalTransformation #MedTech #RegulatoryCompliance

Cantor BioConnect, a global contract research organization (CRO) in the USA, realized they needed an upgrade when their sponsors started asking for a clinical trial management system. Their previous solution no longer met the requirements to efficiently manage their global clinical trials. After identifying key needs in compliance, cost, and collaboration, they turned to ResearchManager for a secure, reliable, and cost-effective CTMS. Discover how ResearchManager delivered: ✅ Advanced compliance with GCP, HIPAA, GDPR, and more ✅ A tailored, budget-friendly solution ✅ Collaborative support to meet their specific needs Since adopting ResearchManager, Cantor BioConnect has boosted their authority with sponsors and secured more deals. Curious to learn more? 👉 Read the full case here: https://lnkd.in/epwRkQQ3 #CustomerCase #ClinicalTrials #CRO #ResearchManager #CTMS #Compliance #Collaboration #Pharma #Healthcare #Biotech #SuccessStory #CustomerCase #ClinicalTrials #CRO #ResearchManager #CTMS #Compliance #Collaboration #Healthcare #Pharma #Biotech