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Automate the manual clinical disclosure tasks that are holding you back. Submit trial information more quickly and accurately, and simplify and optimize your entire clinical trial disclosure process with Citeline Regulatory's TrialScope Disclose: https://ow.ly/Ww0e50T8WXI.
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Join the conversation, become informed and learn how you can contribute to co-create a healthier future all. We can do so much more together to impact lives of all patoents!
Don’t miss out! There are only two days left to register for the first webinar in the DDF Solution Showcase series, cohosted by TransCelerate and CDISC. Join us on Thursday, September 26, along with sponsor companies, clinical solution providers, and key industry stakeholders to explore protocol digitalization solutions. Panelists: Kåre Hyttel, R&D Solutions Principal Consultant, NNIT Sam Thompson, Regulatory Advisory Managing Consultant, NNIT Brittany Walker, Clinical Advisory Managing Consultant, NNIT Ali Dootson, Head of Clinical Integrity, EQTY Life Sciences & ClinLine Berber Snoeijer, Manager of Innovative Process and Solution Design, EQTY Life Sciences & ClinLine Register: https://lnkd.in/eDfVVUm5
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The future is bright
Today, we are excited to announce the acceptance of our regulatory filing that allows us to begin our Phase 1 clinical trial with SAT-3247. We look forward to beginning enrollment in the study and dosing our first participant. Read the release for more details: https://lnkd.in/gRahBT-y #raredisease #rarediseases #smallmolecule #regenmed #regenerativemedicine
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With the new ABPI Code landing this week, join us for our webinar this Friday. #pharma #compliance #pmcpa #abpi
📢 Exciting news! The Prescription Medicines Code of Practice Authority has published the 2024 ABPI Code! This important document (https://lnkd.in/euDW9tdV) outlines the ethical and professional standards that the pharmaceutical industry must adhere to. 📅 Join us for our upcoming webinar on 27th September 2024 at 12:00 PM BST where we'll delve into the key changes and discuss how they impact your business. We'll provide expert insights and practical guidance to help you navigate the new requirements. *Please note that the 2024 Code comes into effect on 1st October, with a transition period until 31st December 2024. During this time, activities can comply with the 2021 Code. On January 1st, 2025, only the 2024 Code will apply. #ABPICode #PharmaceuticalCompliance #IndustryUpdates #pharma #pmcpa 👇 Don't miss out! Register now:
Navigating the New 2024 ABPI Code
events.meddigital.com
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📢 Our webinar, "Navigating the New 2024 ABPI Code" is coming up soon! Join us on 27th September 2024 at 12:00 PM BST! In this webinar, Dr Felix Jackson will discuss: - What the new changes are - How they will affect your day to day activities - Answer any questions you may have regarding these new changes Don't miss this opportunity to get expert insights and practical guidance. *Please note that the 2024 Code comes into effect on 1st October, with a transition period until 31st December 2024. During this time, activities can comply with the 2021 Code. On January 1st, 2025, only the 2024 Code will apply. 👇 Secure your spot now #ABPICode #PharmaceuticalCompliance #IndustryUpdates #pharma #pmcpa
Navigating the New 2024 ABPI Code
events.meddigital.com
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This is such a hot topic right now, as a health plan this is a hard decision to make for so many reasons. A great webinar to listen to.
Didn’t get a chance to catch our webinar on GLP-1s? Watch the recording here! Host, Bruce Flunker President of 90 Degree Benefits Minnesota/Wisconsin, is joined by our guests from Leaf Health, Warren Borders, CSFS®, SVP of Client Engagement, and Jeff Auten, Director of Clinical Consulting, in an engaging discussion about drug cost containment strategies. https://hubs.li/Q02nx8bG0
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Have you heard about Digital Data Flow? TransCelerate BioPharma Inc. has been on this journey since 2014 with their #CommonProtocolTemplate Initiative. The goal is to advance the drug development process by enabling clinical trial protocol digitalization and leveraging the CDISC's Unified Study Definitions Model (#USDM) which allows for a much greater machine-readable structure than other industry-standard formats (and of course, the usual PDFs/documents). Benefits for pharmaceutical sponsors, third party providers, site and regulators include: · Reduced time for manual curation, data entry, and system set-up during study start-up · Improving data reliability and quality · Possibility for automated analytics, #AI / #ML-assisted smart study design, budgeting, feasibility, patient eligibility matching, and patient burden scoring NNIT is a part of an upcoming presentation for this Thursday (my great colleagues Kåre Hyttel, Sam Thompson, and Brittany Walker 😊) sign up to listen in. There's so much to go over from #USDM to #FHIR, I'll be sharing more closer to the date.
Don’t miss out! There are only two days left to register for the first webinar in the DDF Solution Showcase series, cohosted by TransCelerate and CDISC. Join us on Thursday, September 26, along with sponsor companies, clinical solution providers, and key industry stakeholders to explore protocol digitalization solutions. Panelists: Kåre Hyttel, R&D Solutions Principal Consultant, NNIT Sam Thompson, Regulatory Advisory Managing Consultant, NNIT Brittany Walker, Clinical Advisory Managing Consultant, NNIT Ali Dootson, Head of Clinical Integrity, EQTY Life Sciences & ClinLine Berber Snoeijer, Manager of Innovative Process and Solution Design, EQTY Life Sciences & ClinLine Register: https://lnkd.in/eDfVVUm5
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It’s great for teaching about clinical trials … well basis of my interns talk … and so relevant today … took 50 years to implement, costs were a barrier and we still have shockingly high rates Vit C deficiency… citrus deserts. Exciting to see Lindus Health take on transforming trials!#LindusHealth #cro #clinicaltrials #clinicalresearch “Although the results were clear, Lind hesitated to recommend the use of oranges and lemons because they were too expensive. It was nearly 50 years before the British Navy eventually made lemon juice a compulsory part of the seafarer's diet, and this was soon replaced by lime juice because it was cheaper.” Bhatt A. Evolution of clinical research: a history before and beyond james lind. Perspect Clin Res. 2010 Jan;1(1):6-10. PMID: 21829774; PMCID: PMC3149409. Crook J, Horgas A, Yoon SJ, Grundmann O, Johnson-Mallard V. Insufficient Vitamin C Levels among Adults in the United States: Results from the NHANES Surveys, 2003-2006. Nutrients. 2021 Oct 30;13(11):3910. doi: 10.3390/nu13113910. PMID: 34836166; PMCID: PMC8625707.
Today we celebrate the birthday of James Lind, who conducted the first documented clinical trial! In his experiment, he was able to prove that citrus fruits cured scurvy. This is the inspiration for our name, logo, and proprietary eClinical software - Citrus™! 🍊 Interested in how we help sponsors in their journeys in bringing novel therapies to the hands of patients? Send us a DM! #cro #clinicaltrials #clinicalresearch #healthcareinnovation
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🗞️🖥️ In this weeks #POCWeekly newsletter.. A special, in-depth article on Truvian Health’s latest milestone A $74M Raise + how Truvian are now targeting an end of year FDA submission for their POC Analyzer. Stay ahead of the curve with the latest insights and updates in the world of point of care diagnostics. Sign up now in the comments below or by scanning the QR Code to receive your copy and be part of the conversation!
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Today we celebrate the birthday of James Lind, who conducted the first documented clinical trial! In his experiment, he was able to prove that citrus fruits cured scurvy. This is the inspiration for our name, logo, and proprietary eClinical software - Citrus™! 🍊 Interested in how we help sponsors in their journeys in bringing novel therapies to the hands of patients? Send us a DM! #cro #clinicaltrials #clinicalresearch #healthcareinnovation
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