Reliant Health Partners’ Post

Want to build a top-performing Medical Excellence group? Watch our trending video to discover the strategies and benchmarks top biopharma companies use to maximize impact and efficiency 🎥👇 https://lnkd.in/duEMyH6Z Learn how industry leaders are structuring their Medical Excellence teams and overcoming the biggest challenges, from budget allocation to staffing and reporting. 📊 👍 Subscribe to our YouTube channel for more such content! #MedicalExcellence #MedicalAffairs #MedAffairs #MedExcellence #Pharma #Biopharma #Healthcare #BestPracticesLLC

It’s almost time for the 12th Annual Outsourcing in Clinical Trials: Medical Devices Europe Conference! As the key meeting place for healthcare pioneers and innovators, this is a great chance to network with industry peers and solutions providers. Visit us at booth 13 to hear how IQVIA can help to streamline your clinical processes and accelerate your trial timelines. https://bit.ly/3S0Uop6 #OCTMedDevice #MedDevicesEurope #MedicalDevicesEurope #ClinicalTrials

CEOs, CFOs: is your line item for Employee Benefits growing faster than your sales? Are you looking for more control and cost containment for your medical and prescription drug spend? Listen to Joe Parrilli of Captive Resources, LLC explain why more businesses are turning to Member Owned Group Captives to increase transparency, reduce volatility, and overall lower one of their biggest costs. #management #leadership #humanresources #economics

👇🏼This is worth a quick read.. 🚀 More transparency and pragmatism coming from #MHRA and it’s good to see. Medicines and Healthcare products Regulatory Agency #UKMDR #medicaldevices #ukmarket #medtech #ai #ukroadmap

Unlocking the Future of Drug Development Using 505(b)(2)s to generate Real World Evidence (RWE) 🚀The 21st Century Cures Act has paved the way for innovative approaches in measuring the clinical benefits of therapeutic products. Traditional clinical trials often exclude the very patients who need these drugs the most. This is where Real World Evidence (RWE) steps in, bridging the gap between clinical research and real-world medical care. Our latest publication on 505b2.org delves into the importance of pragmatic research and how it can revolutionize healthcare by providing more accurate data for physicians and payers. Learn how expanding beyond laboratory conditions can help reduce healthcare costs and improve patient outcomes.🔗 Read the full article here: https://lnkd.in/eWWNwgd. #DrugDevelopment #RealWorldEvidence #HealthcareInnovation #ClinicalResearch #21stCenturyCuresAct

Getting a Medical Device to market is no small feat for any size of organization. At Apsis Consulting Group, we follow a 5-Step process to get your medical device to market as efficiently as possible. What are some key phases and how low should you expect them to take? Check out this infographic.

Tune in to our recent MedTech Matters episode where we explore the nuances of Notified Body feedback. Our featured expert, Adrian Keene from NAMSA, provides essential tips on navigating feedback and outlining best practices for successful submissions, including: -Detailed device information -Evidence of clinical benefits -Clear safety and performance objectives 🎥 Catch the episode now and gain valuable knowledge for your regulatory strategy! https://lnkd.in/gdQYYnUG #MedTech #CEcertification #NotifiedBody #NAMSAKnows #MedicalDevices #RegulatoryAffairs

Looking for a HUGE lever to boost growth? Find out when to engage reimbursement experts to grow your addressable market sustainably. A complex question in a complex area: When to engage reimbursement experts? #reimbursement #medtech #growth #medtechmarketing

Does your site need more than just a CTMS to accurately track enrollment, site activity, trial opportunities, timing, and performance across your clinical trial operations? Discover why the industry's leading sites and site networks have adopted PROPEL, a comprehensive Business Process Improvement platform designed for research site organizations. #clinicaltrials #clinicalresearch #clinicaltrialsoftware

I'm delighted to share that the second edition of our popular introductory guide: ‘Market access stakeholders and processes for medical devices in key European markets and the USA’ is now available. My colleague, Michelle James (Consultant – Market Access), has updated the guide with European market insights for 2024/25 and added a new section covering the US market. Request your copy by completing the form at: https://lnkd.in/eD_YecMM The guide offers an overview of the reimbursement landscape for medical devices in: ✅ Germany ✅ France ✅ UK ✅ Italy ✅ US It highlights the differences between selected markets and provides a go-to guide for those looking to bring medical device innovations to Europe and the US. #medicaldevices #Medtech #marketaccess #commercialisation #launch #reimbursement