Faro Health Inc.

We’re excited to see everyone next week in San Diego for our 3rd Annual Faro Company Retreat! 2024 has been an incredible year of growth for Faro, and we can’t wait to see what 2025 will bring. A huge thank you to all the Faro employees for your hard work and dedication—your contributions have made this year amazing. We can’t wait to celebrate with you all next week!

The Faro team is going to #OCT San Diego next week, September 24-25! Will you be there? Reach out to Kimberly Connelly Pospahala to schedule time to connect with her and the team! #clinicaltrials #clinicaldevelopment #OCTSanDiego

📣 It's a big week of exciting announcements here at Faro! Introducing Co-Author - our newest offering for generative AI protocol writing! If you caught our CTO Patrick Leung's talk at DPHARM, you'll know that Co-Author builds on the foundation of Faro's Study Designer, which provides the structured, data-based definition of the study necessary for high-quality, error- and hallucination-free document generation. Co-Author is now available for select customers, with general availability in early 2025. Interested to learn more, or be one of the first customers to take advantage? Read all about our approach below, and reach out to our team to schedule a conversation! https://lnkd.in/gjHtn_4f #clinicaldevelopment #clinicaltrials #medicalwriting #clinicalprotocols #genai #protocoldesign

Did you hear the news? Faro is excited to officially share that we've joined the Veeva Systems Product Partner Program! Yesterday, Faro's CEO Scott Chetham announced our partnership with Veeva from the stage at #DPHARM. Through this collaboration, Faro will develop an integration between Faro’s Study Designer and Veeva Vault EDC. This represents one of the first integrations between a digital-native study designer and an EDC system, marking an important milestone in the biopharma industry’s ongoing efforts to increase efficiency, connect data flow, and improve data-driven decision-making in clinical development. Read the full press release here: https://lnkd.in/gfDad8ye Want to learn more? If you're at DPHARM, stop by Booth 42 today. Otherwise, reach out to the Faro team through our website to connect! #DPHARM2024 #Clinicaltrials #Clinicaldevelopment #veevapartner

It’s already shaping up to be a successful Day 1 of DPHARM! If you’re here, stop by booth #42 for to learn more about our Study Designer and our new generative AI protocol authoring features, or catch our CEO Scott Chetham speaking before DPHARM Idol at 4:40! #clinicaltrials #clinicaldevelopment #dpharm2024

Did you miss yesterday's webinar with Patrick Leung on how AI is transforming clinical development? Don't worry, you have options! 💻 Visit the link below to register and view the recording at your convenience *OR* 💡 Join us next week at DPHARM in Philadelphia to hear from us directly! We've got more exciting news coming next week, so stay tuned for more! https://lnkd.in/gTxJy24e #clinicaldevelopment #clinicaltrials #ai #clinicaloperations #medicalwriting

Check out the latest updates from Faro Health Inc.! 🔊 #dpharm2024 #clinicaltrials #clinicalprotocols

Dr Scott Chetham, CEO and Co-Founder of Faro Health Inc., reveals the untapped potential of data and analytics in clinical protocol design. "When you start to think about protocols as data, you start to imagine all of the possibilities for how you could harness that data, all of the opportunities currently being left on the table." Read the full interview here: https://lnkd.in/ezsiaHwX #clinicalresearch #clinicaltrials #clinicalprotocols

Check out Dpharm latest newsletter - featuring Faro Health Inc.! Wondering what we have been up to this year; find out now! https://shorturl.at/jVcTo #Dpharm2024 #Clinicaldevelopment #AI

In two weeks, Faro Health Inc. will be at DPharm with Patrick Leung, discussing how to Harness Generative AI for Clinical Protocol Authoring. Join us to explore: - The complexities and technicalities of clinical trial protocol documents, and why general AI models often struggle with producing high-quality, error-free content. - How integrating a detailed, structured data model tailored to the clinical trial domain can dramatically accelerate protocol authoring while enhancing accuracy and quality. - Discover how your organization can effectively leverage generative AI to improve your clinical protocol authoring process, and learn how to critically evaluate AI-based solutions to meet your needs. Tuesday, September 17th at 11:45 AM EST: Track D #DPharm2024 #DPharmIdol #ClinicalInnovation #ClinicalTrials