ProofPilot ’s Post

🚨Think GxP compliance doesn’t matter in patient recruitment? Think again! 🚨 Patient recruitment is more than outreach - it’s about trust, safety, and integrity. 🙏🏼 While some argue that GxP doesn’t apply to recruitment, leading pharma companies and regulators see it differently. In our latest blog, our SVP of Customer Success, Lauren Briggs, and our CTO, Brian O'Neill join forces to break down the critical role GxP compliance plays in patient recruitment and why it’s becoming a non-negotiable standard. Check out the blog: https://lnkd.in/etNyGskS As the ONLY end-to-end recruitment vendor with a GxP-compliant system, we’re proud to set the bar for compliance and reliability. Our purpose-built, validated, and audit-ready platform means no last-minute scrambles - just reliable, quality results. 🔥 #GxP #GxPCompliance #patientrecruitment #clinicaltrial #clinicalresearch

Ensure your eClinical vendor meets the highest security standards! This blog provides a detailed checklist for evaluating vendor security measures, covering governance, risk assessment, compliance, and more. Protect your clinical data with confidence. Read now: https://hubs.li/Q02ykVz-0 #eClinical #DataSecurity #Cloudbyz #pharmacovigilance #healthcare #CTMS #eTMF #RTSM #Safety #PV #Pharmaceutical #Biotechnology #MedicalDevices #Diagnostics #Cloudbyz #ClinicalTrials

Ensure your eClinical vendor meets the highest security standards! This blog provides a detailed checklist for evaluating vendor security measures, covering governance, risk assessment, compliance, and more. Protect your clinical data with confidence. Read now: https://hubs.li/Q02ykYkV0 #eClinical #DataSecurity #Cloudbyz #pharmacovigilance #healthcare #CTMS #eTMF #RTSM #Safety #PV #Pharmaceutical #Biotechnology #MedicalDevices #Diagnostics #Cloudbyz #ClinicalTrials

Ensure your eClinical vendor meets the highest security standards! This blog provides a detailed checklist for evaluating vendor security measures, covering governance, risk assessment, compliance, and more. Protect your clinical data with confidence. Read now: https://hubs.li/Q02yk-Jm0 #eClinical #DataSecurity #Cloudbyz #pharmacovigilance #healthcare #CTMS #eTMF #RTSM #Safety #PV #Pharmaceutical #Biotechnology #MedicalDevices #Diagnostics #Cloudbyz #ClinicalTrials

Ensure your eClinical vendor meets the highest security standards! This blog provides a detailed checklist for evaluating vendor security measures, covering governance, risk assessment, compliance, and more. Protect your clinical data with confidence. Read now: https://hubs.li/Q02ykVWp0 #eClinical #DataSecurity #Cloudbyz #pharmacovigilance #healthcare #CTMS #eTMF #RTSM #Safety #PV #Pharmaceutical #Biotechnology #MedicalDevices #Diagnostics #Cloudbyz #ClinicalTrials

"We don't need to be GxP compliant until the patient is Consented" - not anymore 🚫. Leading pharma companies now demand compliance during recruitment! In this blog, we break down: 🔥Why GxP compliance is no longer just for in-study activities 😱 The risks of skipping compliance in patient recruitment ✔️How a compliance-first approach future-proofs recruitment efforts Read more - link in comments ⬇️ #clinicaltrials #patientengagement #gxpcompliance #clinicalresearch

White-collar discrepancies on the rise! 📊 Key industries facing major challenges: Telecommunication leads with 18.2%, while Pharma & Medical follows closely at 17.1%. Staying vigilant with background checks is more critical than ever. 🔍 #BackgroundVerification #IndustryInsights #RiskManagement

Ditch tactical inefficiency, and manage your venue data, relationships and compliance better in our back-end database. Contact us to chat through the options to help your business. #SMM #PreferrredProgrammes #Corporates #meetingplanners #PCO #EventsAgency #MedicalCommunications #compliance #pharma #medicaldevices

In the fast-paced world of clinical research, efficiency, security, and regulatory compliance are paramount. E-signatures are revolutionizing clinical trials by addressing critical challenges in documentation, approval processes, and global collaboration. With the U.S. FDA’s 21 CFR Part 11 ensuring the reliability and legality of electronic records, organizations can now streamline workflows, enhance security, and accelerate trial timelines without compromising data integrity. At Mushroom Solutions, we provide an advanced e-signature platform designed specifically for clinical research. With features like multi-factor authentication, real-time audit trails, and encrypted secure storage, our platform ensures full compliance with FDA regulations and optimizes trial management. From informed consent forms to regulatory submissions, Mushroom Solutions makes document management faster, more secure, and cost-effective. Discover how our platform can transform your clinical trial workflows and drive operational efficiency. Learn more: https://bit.ly/41MWTBW #ClinicalTrials #ESignatures #RegulatoryCompliance #FDA #21CFRPart11 #ClinicalResearch #DigitalTransformation #Innovation #HealthTech #Automation #Compliance #GlobalCollaboration #DataSecurity #MushroomSolutions #Pharmaceutical #ClinicalTrialManagement #GCP #AuditTrail

Challenges with External Vendors in Clinical Trials: Why Service Quality is Critical, Yet Often Falls Short In the development of a drug and medical device, services are often required from a wide range of external vendors. Vendors such as CROs, central laboratories, EDC and IRT providers, logistics management systems, pharmacovigilance services, imaging data storage and analysis systems, drug and lab kit manufacturing and storage suppliers, and more. The consequences of insufficient oversight can include delays, unexpected costs, significant risks to patient safety, and jeopardizing the drug or device development process. A detailed Vendor Oversight Plan and strong personal relationships with each vendor are essential to ensure proper performance and adherence to high standards. Without this, vendors will prioritize clients who provide this level of oversight, which can result in your project being neglected due to time constraints. The key principle is to raise clients' awareness of the level of oversight required on their part to ensure success. Effective oversight and management can make the difference between success and failure – ensuring high-quality and efficient service throughout the entire process. At Myrtle, this is our area of expertise. Whether you're starting a project or already in the midst of one and feeling like things are out of control – reach out. We excel in this area and would be pleased to support you in bringing order and predictability to the process It is also important to note that there are vendors who demonstrate high professionalism and excellent results even without close oversight. I would be happy to recommend them ✨ #ClinicalOperations #ClinicalTrials #VendorManagement #TrialSuccess #MyrtleCRO