📢 This just in: The #FDA has approved #Opill (norgestrel) as the first nonprescription daily oral contraceptive, a convenient and accessible option for preventing pregnancy without a prescription. #WomensHealth #ReproductiveHealth #Healthcare Read more: hubs.ly/Q01XGDdv0

We’re sponsoring the Greenlight Guru Risk Management True Quality Summit Series to give medical device professionals a chance to collaborate, learn, and find inspiration. It’s 100% free and 100% virtual - grab your seat here: hubs.ly/Q01XYTJW0

Looking to learn about Navigating AI Risks for Regulatory Approval in Medical Devices? Our own Isabella Schmitt will be live at the Risk Management True Quality Summit Series on July 20th. Grab your seat: hubs.ly/Q01YdwRK0 #RiskTrueQualitySummit #RiskResilience2023

📢 It's time for a Weekly Briefing led by Grace Cuillier. 🎥 Learn about #FDA designations: Registered, Cleared, Granted, Authorized, and Approved. Gain insights to steer your product efficiently and compliantly. #Healthcare #MedicalDevices hubs.ly/Q01YnvxV0

🏆 Thrilled to announce that Proxima's "An Innovator's Journey" video won Platinum at the dotCOMM Awards! 🌟 Kudos to our team for their exceptional work in digital storytelling! hubs.ly/Q01YGJ860 🎉 #dotCOMMAwards #PlatinumWinner #Innovation #ClinicalResearch

📢 Our CEO, Kevin Coker, is at the renowned DxPx Conference Anaheim, where diagnostics and precision medicine innovators, investors, and industry leaders converge! Proud to be part of this cutting-edge event! #DxPxConference #PrecisionMedicine #Diagnostics #Innovation #aacc2023

🔬 Meet Dr. Alex Spira, CEO & Clinical Director for NEXT Oncology Virginia! 🌟 Dr. Spira drives breakthroughs in cancer care and provides hope to patients with advanced cancers. We value his contributions in our EPON network! #Oncology #CancerResearch #ClinicalTrials

🎙️ Rob MacCuspie, Manager of Regulatory & Quality Affairs at Proxima Clinical Research, shares insights on building a QMS in Greenlight Guru's Global Medical Device Podcast. Tune in now on iTunes/Spotify! 👉 #MedicalDevice #Podcast #QMS hubs.ly/Q01ZqJjs0

🙏 Thank you, @InnovationMap, for featuring us! #ClinicalTrials #Oncology #CancerTreatment #EPON #InnovationMap #MedTech #Houston #HealthcareNews hubs.ly/Q01ZFMhx0

🔬 Curious about the role of Notified Bodies in the EU for medical device development and marketing? Join us for this week's Weekly Briefing, featuring Ellie Reynolds, Associate Director of Regulatory Affairs. hubs.ly/Q01ZYYSd0 #MedicalDevices #EURegulations #Healthcare

🌟 Big News: FDA Approves Zurzuvae (zuranolone) for Postpartum Depression, offering hope to new moms battling postpartum depression. A game-changer for mental health. 💙 #FDAApproval #Zurzuvae #MentalHealth #Innovation Read more here: hubs.ly/Q01-CH5f0

🏆 Proxima CRO makes the Inc. 5000 List for the second year in a row and lands the Platinum Award at dotCOMM Awards for our video "An Innovator's Journey." 🎥 Kudos to our amazing team! #Innovation #Excellence #Inc5000 #dotCOMMAwards hubs.ly/Q01_5gFd0

Hear from Chester Koh, Executive Director of SWPDC, as he shares his experience collaborating with Proxima. Discover how our partnership is driving pediatric device innovation and making a real impact in healthcare! hubs.ly/Q01_DYCC0 #ClientTestimonial #HealthcareInnovation

🔍 Delve into Investigational Device Exemptions (IDEs) in our latest "Weekly Briefing" with Grace from Proxima Clinical Research. Discover their role in clinical studies and the steps to obtain one. hubs.ly/Q02080CM0 #WeeklyBriefing #IDEs #ClinicalStudies

📅 Save the date: Oct 4th! Join this webinar with Proxima, Velentium, and Greenlight Guru to discover how collaboration shapes the future of medical devices. Real-world case studies, integration strategies, and more. Don't miss it! 👉hubs.ly/Q022g1T40 #MedTech #Innovation

🤔 Curious about using unapproved medical devices to save lives in critical conditions? Join us this week for a deep dive into Expanded Access! 🚀 Watch now! #ExpandedAccess #MedicalDevices hubs.ly/Q022Khz50

🌟 Embracing MedTech Innovation at #LSIEurope23! 🚀 This week Proxima CRO joined industry leaders at LSI Europe '23, where Isabella Schmitt introduced Proxima and other dynamic companies during her session. Thank you to LSI - Life Science Intelligence™ 📢 #MedTechInnovation #MedTech

Ready to ace your device submission? Weekly Briefing time! 🚀 Ellie Reynolds explores Pre-submissions—the secret to a smoother regulatory journey. Gain a competitive edge for your 510(k), De Novo, or PMA submission. Tune in! #FDA #MedTech #RegulatoryTips hubs.ly/Q023z68y0

Diving into Regulatory Nuances! 🌐 Ever wondered about the intricate requirements for clinical investigations of marketed drugs or biologics? hubs.ly/Q024-4xH0 Explore the fine print of 21 CFR 312.2(b)(1) for regulatory insights! 📚 #RegulatoryAffairs #FDACompliance #FDA

Unraveling ANDA: The key to generic drug approval! 🗝️ Join us on a journey through Abbreviated New Drug Application essentials. 🚀 Ready to make your mark in drug development? Reach out to Proxima for guidance! 🌐 #PharmaInsights #ANDA #DrugDevelopment hubs.ly/Q025D6h70