There's a few days left for you to register for our #Boston dinner event on Tuesday, Sept. 10. The #pharmaceuticalsecurity discussion will feature insights from Dean Geribo of Moderna, Nicole Orne Markovic from Foundation Medicine, and Jonathan Brooks, CPP from Alkermes (with Ryan Schonfeld as moderator). Register to attend: https://hubs.ly/Q02NSFWz0 #pharma #securityindustry #securityoperations #security
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A few of the potential benefits of microneedle: -rapid uptake of drug into the body, faster than IM/sub-Q -no needle -at home administration -room temperature storage Kindeva has commercial manufacturing capabilities. This webinar is a good start to understanding the developments in MAP.
Curious about intradermal delivery? There’s still time to join us today at 10 a.m. ET for this webinar, sponsored by the PDA Vaccine Interest Group. Explore the technology, clinical evidence, manufacturability, and scalability of microneedle array patches with Kindeva’s Vice President, Dermal Delivery and Licensing, Andy Riso, and Scientific Director, Dermal Drug Delivery, Tim Peterson, alongside James Birchall from Cardiff University / Prifysgol Caerdydd and Mahmoud Ameri. https://lnkd.in/gKhDYcBi #microneedles #combineforces #drugdelivery PDA - Parenteral Drug Association
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We’re thrilled to join the Anticoagulation Forum’s Corporate Council! At Cadrenal Therapeutics, Inc. (Nasdaq: CVKD), we are proud to align with the Anticoagulation Forum (AC Forum). With 15,000 healthcare professional members, AC Forum is the largest organization dedicated to advancing anticoagulation care globally. Our participation reflects our shared commitment to innovation, educational initiatives, and improving patient outcomes. With our development of tecarfarin, a new vitamin K antagonist (VKA), we aim to address gaps in chronic anticoagulation therapy and provide a superior and safer option for patients with left ventricular assist devices or rare cardiovascular conditions. We look forward to collaborating with the AC Forum’s thought leaders and contributing to initiatives that share research findings, promote best practices and advance patient outcomes. #HealthcareInnovation #Anticoagulation #ACForum #Pharma #PatientOutcomes #CadrenalTherapeutics #LVAD
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Exciting News for Nuclear Medicine! A new rule proposes to unbundle diagnostic radiopharmaceuticals from the current payment system, classifying them separately from "supplies." This will prevent CMS from overpaying for low-cost diagnostics and offer patients access to advanced imaging agents. #nuclearmedicine #radiologynews #healthcare #compuraymedical
There's a new proposed rule that unbundles diagnostic radiopharmaceuticals from the current packaged payment system that classifies them as "supplies." The new rule will prevent CMS from overpaying for low-cost diagnostic radiopharmaceuticals and give patients access to a more precise generation of imaging agents. SNMMI will be submitting a comment in support of the CMS rule and is celebrating this win for patients! Learn more below and on our website: https://lnkd.in/dkPjWqXa
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Chief Financial Officer at Cadrenal Therapeutics, Inc. (Nasdaq: CVKD) - advancing its late-stage drug candidate tecarfarin, a new blood thinner for patients with implanted cardiac devices and rare CV conditions
We’re thrilled to join the Anticoagulation Forum’s Corporate Council! At Cadrenal Therapeutics, Inc. (Nasdaq: CVKD), we are proud to align with the Anticoagulation Forum (AC Forum). With 15,000 healthcare professional members, AC Forum is the largest organization dedicated to advancing anticoagulation care globally. Our participation reflects our shared commitment to innovation, educational initiatives, and improving patient outcomes. With our development of tecarfarin, a new vitamin K antagonist (VKA), we aim to address gaps in chronic anticoagulation therapy and provide a superior and safer option for patients with left ventricular assist devices or rare cardiovascular conditions. We look forward to collaborating with the AC Forum’s thought leaders and contributing to initiatives that share research findings, promote best practices and advance patient outcomes. #HealthcareInnovation #Anticoagulation #ACForum #Pharma #PatientOutcomes #CadrenalTherapeutics #LVAD
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We’re thrilled to join the Anticoagulation Forum’s Corporate Council! At Cadrenal Therapeutics, Inc. (Nasdaq: CVKD), we are proud to align with the Anticoagulation Forum (AC Forum). With 15,000 healthcare professional members, AC Forum is the largest organization dedicated to advancing anticoagulation care globally. Our participation reflects our shared commitment to innovation, educational initiatives, and improving patient outcomes. With our development of tecarfarin, a new vitamin K antagonist (VKA), we aim to address gaps in chronic anticoagulation therapy and provide a superior and safer option for patients with left ventricular assist devices or rare cardiovascular conditions. We look forward to collaborating with the AC Forum’s thought leaders and contributing to initiatives that share research findings, promote best practices and advance patient outcomes. #HealthcareInnovation #Anticoagulation #ACForum #Pharma #PatientOutcomes #CadrenalTherapeutics #LVAD
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Veteran marketing research/healthcare data professional with broad pharmaceutical, biotech and medical device experience, spanning multiple therapeutic areas and a variety of marketing contexts.
BMS is poised to enter the Eosinophilic Esophagitis (EoE) market. Buried in the BMS Q2 2024 earnings call was news that company's eosinophilic esophagitis (EoE) treatment, cendakimab, successfully met Phase 3 clinical endpoints. Similar to already-approved, Dupixent, cendakimab is a biologic with subcutaneous injections every other week. Specifics on the data have yet to be released, this new agent could pose some competitive pressure for Dupixent in EoE. #gastroenterology #clinicaldata https://lnkd.in/g_2a2MWv
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Today Liquidia Corporation announced that it has filed litigation challenging the FDA’s decision to grant clinical investigation exclusivity to a competing product. This follows the tentative approval of YUTREPIA for the treatment of adults with PAH and PH-ILD. Dr. Roger Jeffs, Ph.D., Chief Executive Officer of Liquidia, said: “The FDA’s action improperly allows United Therapeutics to tack on yet another regulatory exclusivity, stifling competition and patient choice. This decision violates clear congressional intent to allow NCI exclusivity only for true innovations that are supported by new clinical studies that demonstrate safety and/or efficacy of the innovation. It is our strong belief that the FDA’s decision to grant Tyvaso DPI this new NCI exclusivity should be vacated, and Liquidia should be allowed to bring YUTREPIA to market for the benefit of patients immediately.” Read more here: https://bit.ly/4fTP1U2
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Make use of our experts on patient recruitment and feasibility at the Nordic Life Science Days in Malmö next week! On 18-19 September, Simon Klaasen and Ola Hasselgren will be there, ready to share their expertise in patient recruitment and feasibility studies. Whether you’re in the early stages of planning a clinical study or already writing your protocol, stop by our booth to explore how we can help boost your recruitment efforts. Did you know? Our patient feasibility studies can provide crucial patient feedback before you even begin. By incorporating patient insights early, you can optimize your study and reduce the overall budget—saving time and resources while increasing your study’s success rate. Don’t miss this opportunity to meet with us at NLSDays! Let’s discuss how we can make your next clinical trial more efficient and patient-focused. Visit us at our stand or learn more at www.link2trials.com . Follow us! #NLSDays #PatientRecruitment #ClinicalTrials #FeasibilityStudies #CRO #Pharma #MedTech #InvestInPatients #NordicStars #ClinicalExcellence #Link2Trials
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Time to comment has started! Let’s do this! Long time coming, and significant amount of lobbying to get us to this point. Kudos!! 🤞🤞🤞🤞🤞🤞🤞🤞🤞 #radiopharmaceuticals #nuclearmedicine #theranostics #radioligandtherapy #radiology #precisionmedicine
There's a new proposed rule that unbundles diagnostic radiopharmaceuticals from the current packaged payment system that classifies them as "supplies." The new rule will prevent CMS from overpaying for low-cost diagnostic radiopharmaceuticals and give patients access to a more precise generation of imaging agents. SNMMI will be submitting a comment in support of the CMS rule and is celebrating this win for patients! Learn more below and on our website: https://lnkd.in/dkPjWqXa
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If you are attending SCOPE stop by and learn how AliveCor's Kardia devices can optimize your clinical resarch studies!
AliveCor Biopharma will be at #SCOPEsummit to showcase how our ECG solutions are transforming the clinical trial space. Stop by Booth #209 to meet the team and learn about our FDA-cleared ECG technology at the heart of clinical research. We look forward to seeing you there.
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2moLooking forward to this!