Ever wondered how technology can transform the traditional challenges of healthcare? ð¤ Launching a pioneering project on Voice Prescription redefined my perception of innovation in health tech. Faced with the prevalent issue where pharmacists struggle to decipher doctorsâ handwritten notes, our team was motivated to find a viable solution. By integrating Optical Character Recognition (OCR) technology, we enhanced the readability of prescriptions, ensuring accuracy in drug identification and dosage extraction. This journey wasn't just about solving a problem; it was a testament to the power of technology in making healthcare more accessible and error-free. It made me ponder on how many such everyday challenges await innovative solutions. What healthcare problems do you think technology could solve next? #HealthTech #Innovation #EngineerInMaking
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ð Exciting news! My latest article delves into the captivating evolution of pharmacy and the game-changing influence of technology in the wellness industry. From virtual consultations to smart medication adherence tools, technology is reshaping the landscape of pharmacy and wellness. Join me in exploring the dynamic intersection of pharmacy and technology and its profound implications for the future of healthcare. Read the full article and let's continue the conversation on the evolving role of pharmacy in today's tech-driven world! #Pharmacy #Technology #WellnessEvolution
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Just 3 weeks to go until our âRegulatory Strategies for Womenâs Health Technologyâ webinar⦠ On Wednesday 24th July, Psephos and Science & Engineering Health Technologies Alliance (SEHTA) will be hosting a live webinar alongside one of our product advisory and development partners, Sagentia Innovation. We will be discussing the challenges womenâs health start-ups face when developing their commercialisation strategies, particularly when choosing a regulatory pathway. Is it better to take a direct-to-consumer approach? Or should you pursue a regulated medical device pathway?  Book your place below to learn how â and when â to define your regulatory strategy to ensure your next womenâs health innovation is a success.  https://lnkd.in/efEKZUw8  #regulatorycompliance #womenshealth #medtech #medicaldevices
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Learn how and when to define your regulatory strategy to ensure your next womenâs health innovation is a success, in this webinar on July 24. Robin Stephens, Psephos Biomedica and Erica Kantor, Sagentia Innovation will be discussing: - The emerging womenâs health technology landscape - The challenges womenâs health start-ups face when developing and commercialising new solutions - The pros and cons of the direct-to-consumer approach, vs seeking regulatory approval - The key considerations in developing a successful commercialisation strategy Register here: https://lnkd.in/efEKZUw8 Science & Engineering Health Technologies Alliance (SEHTA) #WomensHealth #Regulatory #Medtech
Just 3 weeks to go until our âRegulatory Strategies for Womenâs Health Technologyâ webinar⦠ On Wednesday 24th July, Psephos and Science & Engineering Health Technologies Alliance (SEHTA) will be hosting a live webinar alongside one of our product advisory and development partners, Sagentia Innovation. We will be discussing the challenges womenâs health start-ups face when developing their commercialisation strategies, particularly when choosing a regulatory pathway. Is it better to take a direct-to-consumer approach? Or should you pursue a regulated medical device pathway?  Book your place below to learn how â and when â to define your regulatory strategy to ensure your next womenâs health innovation is a success.  https://lnkd.in/efEKZUw8  #regulatorycompliance #womenshealth #medtech #medicaldevices
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Calling all womenâs health start-ups⦠ On Wednesday 24th July, Psephos and Science & Engineering Health Technologies Alliance (SEHTA) will be hosting a live webinar alongside one of our product advisory and development partners, Sagentia Innovation. We will be discussing the challenges womenâs health start-ups face when developing their commercialisation strategies, particularly when choosing a regulatory pathway. Is it better to take a direct-to-consumer approach? Or should you pursue a regulated medical device pathway?  Book your place below to learn how â and when â to define your regulatory strategy to ensure your next womenâs health innovation is a success.  https://lnkd.in/efEKZUw8  #regulatorycompliance #womenshealth #medtech #medicaldevices
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ð Transforming the Future of Healthcare ð¥â¨ At www.Pharmatching.com, we're dedicated to addressing the evolving needs of patients and healthcare providers alike. As we look ahead to 2024, several key trends are shaping pharma strategies, from legislation changes to technological advancements. ð Key Insights: 1ï¸â£ Patient-Centric Innovations: Patients are increasingly demanding tech-enabled medication services and transparent drug pricing. 2ï¸â£ Integrated Care Expectations: Seamless communication between pharmacies and prescribers is crucial. Patients expect integrated care throughout their health journey. 3ï¸â£ Data Privacy Concerns: With 50% of surveyed patients expressing concern about the privacy of their personal health data, ensuring robust safeguards is more critical than ever. 4ï¸â£ Strategic Investment Areas: Simplified access to price transparency data and incorporating specialty pharmacy data into electronic health records are vital areas for investment. 5ï¸â£ Pharma Evolution: Manufacturers are adapting to meet patient access needs on patientsâ terms, addressing hurdles and transforming patient journeys in novel ways. Join us (www.pharmatching.com) in embracing these changes and driving forward a more patient-focused, transparent, and integrated healthcare system. Together, we can meet the challenges and opportunities of tomorrow. ð©ºð¡ Let's connect and discuss how we can collaborate to revolutionize patient care! ð #HealthcareInnovation #PharmaStrategy #PatientCentric #DataPrivacy #Pharmatching #HealthTech #IntegratedCare
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Thanks to Vittorio Martinelli for sharing this chart about medtech companies. I am surprised to see some companies at the top, but also some at the bottom. What do you think? #medicaldevices #healthcare #medical #medtech
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I can't be the only one who avoids asking pharmacists for medicine, and prefers stuff of the shelf, can I? Relatably, it seems Merck were prepared for people like me when offering a medicine that is newly available over the counter. They asked my colleagues at Innovia Technology to take a holistic approach to the challenge and map out the different biological, medical, behavioural and psychological factors that they should consider when preparing a new launch. Read more about the work over on our Consumer Health Hub: https://lnkd.in/eTRkWKRt #ConsumerHealth #Medication #Innovation
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Managing Partner SS Clini Research LLP | Director Research & Education Dr. RK's | Clinical Research & Educational Consultant | Startup TN Mentor | Adjunct Faculty Saveetha Medical College | Public Speaker & Motivator
ð Unlocking the Future of Healthcare: The Power of Benefit-Risk Analysis in Medical Device Development ð In the dynamic world of medical technology, our top priority is simple: patient safety and efficacy in healthcare innovation. Benefit-risk analysis ensures that every device we create transforms lives safely and efficiently. ⨠Why Benefit-Risk Analysis Matters? ð #PatientSafety: Our analysis ensures innovations improve lives without compromising safety ð #RegulatoryCompliance: Approvals from bodies like the FDA require clear evidence that benefits outweigh risks ð¤ #BuildingTrust: Evaluations build confidence, showing our commitment to excellence and safety ð #ProofofEfficacy: Clinicians trust new devices when rigorous analysis demonstrates clinical benefits, leading to better patient outcomes ð¼ #EthicalCommitment: Beyond compliance, we must ensure our devices offer genuine benefits without causing unnecessary harm ð§ Our Approach to Benefit-Risk Analysis: -Identifying Benefits and Risks: Scrutinizing every clinical improvement and adverse event -Risk Assessment: Prioritizing mitigation strategies by quantifying risks -Benefit-Risk Evaluation: Balancing pros and cons with stakeholder insights. -Risk Mitigation: Implementing design tweaks, clear labeling, and user training -Post-Market Surveillance: Continuously updating analysis based on real-world data By centering benefit-risk analysis in medical device development, we're not just creating products but transforming lives Letâs continue to innovate responsibly and make a lasting impact on global health! Contact us at sscliniresearch@ssshealthcareedu.com SS Clini Research LLP Dr. RK's FDA CDSCO StartupTN Martin King #MedicalDevices #HealthcareInnovation #PatientSafety #RegulatoryCompliance #RiskManagement #FutureOfHealthcare
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Copywriter at DMSI | Virtual Assistant | Laboratory Technician | Product Owner | Website Design & Management | SEO Specialist | Social Media Management
The Future of Laboratory Testing: Innovations to Watch 2. The Rise of Point-of-Care Testing Point-of-care testing (POCT) is gaining popularity due to its convenience and rapid results, allowing diagnostic tests to be conducted near patient care sites like clinics, pharmacies, or even at home. Faster Results: POCT devices provide immediate results, enabling quicker clinical decisions and reducing follow-up appointments. Increased Accessibility: POCT improves access to healthcare, especially in remote or underserved areas. Product Manager Tip: Focus on developing portable, user-friendly POCT devices that deliver quick and accurate results. Partner with healthcare providers and explore direct-to-consumer models to expand market reach. ...
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