EHNOTE

  Orlando, FL – October 2025  – The wait is nearly over. As the ophthalmology world prepares to converge at the  American Academy of Ophthalmology (AAO) 2025  in Orlando, one company is promising to redefine what eye care practices can expect from their technology.  EHNOTE , the only true ophthalmology-centric cloud platform, is gearing up to make a statement at  Booth #3644—right in front of the registration counter. With excitement building across the industry, EHNOTE is not just exhibiting. It is unveiling a bold vision:  a single, unified platform that combines EHR, ASC, PMS, PXM, and RCM into one seamless ecosystem. One Platform. Endless Possibilities. For too long, ophthalmology practices have been forced to juggle multiple systems—  EHRs for patient records  , PMS for administration and reports, a disconnected scheduling system or web forms-where patients easily fall through the cracks, papers for surgical centers, and some generic bil...

  With an aging population, rising prevalence of chronic conditions like diabetes and hypertension, and increasing patient expectations, the demand for  preventive healthcare in ophthalmology  has never been greater. For ophthalmologists, this shift isn’t just about diagnosing and treating eye diseases—it’s about anticipating risks, intervening earlier, and building smarter systems that support long-term vision health. This is where  Ophthalmology EHR software , AI, and advanced data analytics  come in. Together, these tools are transforming how practices identify at-risk patients, manage chronic eye conditions, and deliver personalized care that goes beyond the exam room. Why Preventive Healthcare Matters in Ophthalmology Preventive healthcare focuses on  early detection, proactive monitoring, and lifestyle interventions  that reduce the risk of disease progression. In ophthalmology, prevention can mean the difference between preserved sight and irrev...

  In ophthalmology, time is one of your most valuable resources—second only to clinical precision. And let’s be honest, precision often depends on having enough time in the first place. So, it won’t be wrong to say, time is the most valuable resources. Whether you’re performing a cataract evaluation, planning a  refractive surgery , or managing a chronic dry eye patient, the speed and accuracy of your documentation directly influence both patient experience and clinical outcomes. Yet, for many ophthalmologists, traditional  EHR systems  remain a constant source of frustration. Endless clicking. Repetitive data entry. Navigating through screens that look the same for every visit, regardless of the case. And somewhere in the back of your mind—the worry of missing a crucial detail in the chart. But what if your EHR could work the way you do? What if it could adapt to your specialty, subspecialty, and even the unique flow of your practice? That’s exactly where self-confi...

  Software as a Medical Device (SaMD)  refers to standalone software that performs medical functions (for diagnosis, treatment, monitoring, etc.) without being part of a hardware device. In recent years, such software – especially AI-driven tools – has become widespread in health care. Recognizing the unique risks and innovation potential of SaMD, the FDA (via its Digital Health Center of Excellence) has embarked on a series of new policies and guidance's. In short, the FDA aims to regulate SaMD with a  risk-based, life-cycle approach  that protects patients while enabling innovation. How FDA Regulates SaMD Today The FDA treats SaMD under its existing medical device laws, using established pathways (510(k), De Novo, or PMA) based on risk. Simply put, if a software function meets the definition of a medical device, it is evaluated like any other device. The FDA focuses oversight on higher-risk software (e.g. diagnostic algorithms) and often exercises  enforcement...