All posts by imreal

Aragon Research Publishes New Research Note on How Organizations Should Use the U.S. Executive Order on AI


All organizations with an interest in AI must recognize that while these executive orders hold a direct impact on government agencies, they also present a framework applicable to all organizations and users engaged in harnessing and governing the potential impact of AI,” said Betsy Burton. “Our focus is on providing clear, concise actionable advice within each section that serves as a valuable compass for shaping your organization’s strategic and operational plans.”

This note is a must-read; it meticulously summarizes the immediate executive orders for action that must be implemented, and furnishes a comprehensive foundation for future policies, governance, regulatory requirements and, even, future legislation. Government and private sector entities must understand and take action on the issues highlighted in this executive order and on Aragon Research’s advice when embracing, employing, and fabricating AI systems.

Aragon’s clients can access further details regarding this new executive order and the associated actionable advice by referring to the document titled “How Your Organization Should Use the US Executive Administration Order on AI as a Framework.”

About Aragon Research

Aragon Research delivers high-impact visual research, consulting, and advisory services to provide enterprises the insight they need to make better technology and strategy decisions. Aragon Research serves business and IT leaders and has a proven team of veteran analysts. For more information, visit https://www.aragonresearch.com.

Media Contact

Paula Quiroz, Aragon Research, 650-285-9889, [email protected], Aragonresearch.com 

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SOURCE Aragon Research



GlobalMed Technologies Launches Omnilux Mini, a line of three, FDA-cleared, flexible, portable, and affordable LED devices


The Eye Brightener targets dark circles and wrinkles with 633nm red light and 830nm near-infrared light. The device adheres to the skin with a hydrocolloid patch infused with amino acid-rich peptides and niacinamide for maximum hydration.

The Blemish Eraser fights acne, clears congested skin, and calms redness + inflammation with 415nm blue light and 633nm red light. The device adheres to the skin with hydrocolloid patches infused with salicylic acid and green tea to spot-treat stubborn acne.

The Skin Corrector improves fine lines and appearance of age spots while soothing redness with 633nm red light and 830nm near-infrared light. The device adheres to the skin with hydrocolloid patches infused with vitamin C and azelaic acid to help brighten tone and diminish pigmentation.

Additional hydrocolloid patches are available in packs of 20 for $44.

With over 40 clinical studies proving the effectiveness of its technology, Omnilux is the brand of LED phototherapy systems most recommended and used by dermatologists for in-office treatments. Now, the company is offering consumers the chance to receive that same standard of treatment through affordable, targeted treatment devices. For more information on the company and its products, visit www.omniluxled.com.

Press Contact

Jeneration PR for Omnilux

Sarah Blackledge

1 5046153259

[email protected]

About Omnilux Mini

Omnilux has been recognized as the world leader in medical-grade LED light therapy devices since 2003. Now, the company has an at-home device specifically for the treatment of acne based on its proven technology. Omnilux Mini is a line of three, FDA cleared, flexible, portable, and affordable LED devices that contain 12 individual LEDs, encased in 6 dual chip bulbs for targeted treatment of your most troubling spots. Each Mini device provides professional results from virtually anywhere with three 10-minute treatment sessions per charge. The Eye Brightener targets dark circles and wrinkles with 633nm red light and 830nm near-infrared light. The Blemish Eraser fights acne, clears congested skin, and calms redness + inflammation with 415nm blue light and 633nm red light. And lastly, the Skin Corrector improves fine lines and appearance of age spots while soothing redness with 633nm red light and 830nm near-infrared light. To learn more, or to order online, visit www.omniluxled.com.

About GlobalMed Technologies

GlobalMed Technologies (GMT) is a leading medical technology company based in the San Francisco Bay Area. Specializing in light-based devices used in various clinical and cosmetic applications, throughout its almost 25-year history GMT has manufactured or distributed some of the most recognizable brands in the industry, including Omnilux Medical™, Strata XTRAC™, CoolTouch™, VASER™, BTL™, and Radiancy™.

SOURCE JenerationPR

CAMP in Texas Hill Country offering premier spots to media to film the 2024 Total Solar Eclipse!


We are inviting YOU to broadcast from this beautiful Texas Hill Country vantage point. View this 90-second video to learn more about CAMP and see an aerial view at the end of the video.

As a special guest of CAMP, viewing spots for media are in a stellar location (excuse the pun), with reserved parking for your crew. Many activities will occur throughout the day (after all, that is what we do!) including eclipse-related and camp activities for all ages. Gates open to the public at 7:00 a.m. and close at 6:00 p.m. (to allow traffic to subside). Breakfast, lunch, and snacks will be sold throughout the day.

Total Eclipse at CAMP event tickets (for the general public) are $100 for adults and $50 for children (12 and younger) and include entrance onto CAMP’s property; ISO glasses to safely view the eclipse; spots with clear view of the skies; knowledgeable astrology speakers; and educational and camp activities for families. Parking is additional for the public. While folding chairs are available for media, you are encouraged to bring your own comfortable lawn chairs.

About CAMP:
Since 1979, Children’s Association for Maximum Potential (known locally as Camp CAMP) has provided safe and fun-filled recreational experiences year-round for individuals (ages 5 – 55) with mild to severe disabilities, with diagnoses such as Autism Spectrum Disorder, Intellectual Disability, Cerebral Palsy, Down syndrome, Traumatic Brain Injury, Spina Bifida, visual impairment, and hearing impairment.

Campers are racially diverse with 26% Hispanic, 5% African American, 3% Asian, 1% Native American, 47% Caucasian, and 18% identified as Multi-Race/Other.

On average, CAMP serves over 1,400 individuals with disabilities annually in our summer and school-year programs. As a result of these campers garner independence, self-confidence and encouragement through medically safe recreational activities (like swimming, horseback, canoeing, archery, music recreation, arts & crafts, karaoke and a CAMP dance) and social interactions, while parents and siblings receive well-deserved respite from around-the-clock care of their family member. CAMP successfully adapts activities that allow participants to experience a sense of mobility, independence and fun. Due to the severity of their disabilities, many served by CAMP are not eligible to participate in other camps or programs offered within that community.    

CAMP also provides leadership development for high-school students/young adults, and hands-on educational experiences and CEUs for healthcare professionals. In 2022, 1,429 teen and young adults volunteers dedicated 87,700 hours of service; 152 Healthcare professional volunteers dedicated 15,616 hours of service.

CAMP is located at 515 Skyline Drive, Center Point, Texas 78010.

Please let me know if you are interested so we can save you a spot.

MEDIA CONTACT: Jeanne Albrecht, CAMP Board Member since 2019
210-392-9047
[email protected]

SOURCE CAMP

Pasternack Presents Advanced Rubberduck and Whip-Style Antennas


Particularly, the stubby-style antennas stand out, striking a balance between compactness and top-tier functionality. From the bustling frequency of 2.4 GHz to the distinct 916 MHz, these antennas encapsulate a vast bandwidth catering to multiple wireless needs.

Distinctive features of this innovative range are vast and varied. A broad frequency palette, gains peaking at 4.5 dBi, and designs ranging from the subtle concave to the adaptable tilt and swivel styles, showcase the breadth of this collection. Moreover, with fine-tuned performance in the 4G LTE and 5G realms, these antennas are primed to address the burgeoning demands of next-generation connectivity.

Flexibility remains at the core of Pasternack’s design philosophy. These antennas come equipped with both SMA male and RPSMA connectors, making integration effortless. The inclusion of a 90-degree connector introduces adaptability, and with features such as resilience against water and dust ingress, linear polarization, and the advantage of dual-band Wi-Fi, they stand as unparalleled assets in the antenna domain.

“At Pasternack, we believe in shaping the future of wireless communication,” said Product Line Manager Kevin Hietpas. “Our rubberduck and whip-style antennas are a testament to our unwavering pursuit of excellence and our passion to provide next-level solutions.”

Pasternack’s rubberduck and whip-style antennas are in stock and available for same-day shipping. For inquiries, please call +1 (949) 261-1920.

About Pasternack:

A leader in RF products since 1972, Pasternack is an ISO 9001:2015-certified manufacturer and supplier offering the industry’s largest selection of active and passive RF, microwave and millimeter wave products available for same-day shipping. Pasternack is an Infinite Electronics brand.

About Infinite Electronics:

Infinite Electronics has a global portfolio of leading in-stock connectivity solution brands. Infinite’s brands help propel the world’s innovators forward by working urgently to provide products, solutions and real-time support for their customers. Backed by Warburg Pincus, Infinite’s brands serve customers across a wide range of industries with a broad inventory selection, same-day shipping and 24/7 customer service. Learn more at infiniteelectronics.com.

Media Contact

Peter McNeil, Pasternack, +1 (978) 682-6936, [email protected], https://www.infiniteelectronics.com 

SOURCE Pasternack

Smileyscope Therapy is the First Virtual Reality Device to Receive FDA Class II Clearance for Acute Pain


Smileyscope has made history by becoming the first virtual reality (VR) device to receive FDA Class II clearance for acute pain. This approval recognizes Smileyscope’s innovative Procedural Choreography™ technique, which uses positive virtual stimuli to reduce pain and anxiety during medical procedures. With this milestone, Smileyscope aims to revolutionize pain and anxiety management, partnering with hospitals and clinicians globally to enhance patient experiences and improve clinical workflows.

WASHINGTON, Nov. 6, 2023 /PRNewswire-PRWeb/ — The FDA has granted Class II clearance to Smileyscope™ Therapy, making Smileyscope Therapy the first and only VR Analgesic™ available in the US. Smileyscope is the premier provider of drug-free pain and anxiety treatments for procedures, worldwide.

FDA clearance of Smileyscope’s flagship therapeutic highlights Smileyscope’s position as a leader in Digital Therapeutics. Digital Therapeutics are “a new category of medicine” which “deliver medical interventions directly to patients using evidence-based, clinically evaluated software” (1) achieving clinically important effects. The Digital Therapeutics market is expected to reach 32.5 billion USD by 2030. (2)

Shortly after the close of their funding round, Smileyscope attained another major accomplishment on September 25th, 2023 when FDA cleared their groundbreaking VR system to “temporarily reduce and/or manage pain and temporarily relieve acute procedural anxiety associated with needle procedures.”

FDA clearance included critical, independent evaluation of Smileyscope’s patented Procedural Choreography™. Procedural Choreography is Smileyscope’s proprietary technique that takes negative real-world stimuli (e.g. a needle) and replaces it with psychologically-preferable positive virtual stimuli (e.g. a friendly fish). Granted in 2022, Smileyscope’s Procedural Choreography patent powers an unmatched safety and efficacy profile and underlies future therapeutic products.

Smileyscope’s studies, the world’s largest randomized trials in procedural VR, were reviewed by the FDA during the Class II filing. These demonstrated reductions in child self-rated pain of up to 60% and anxiety of up to 40%, laying the clinical groundwork for this first-ever clearance of a VR device for acute pain and anxiety. Studies also demonstrated benefits of up to 75% in caregiver distress and of up to 48% reduction in the use of physical restraints. (3)

The medical community has rapidly embraced Smileyscope. The Infusion Therapy Standards of Practice (4) uniquely cites Smileyscope’s studies for management of vascular access pain. Smileyscope’s trials are referenced in UpToDate®, the healthcare industry-leading clinical decision resource, as a nonpharmacological intervention which may avoid procedural sedation (5). Only months after the American Medical Association issued CPT® codes recognizing VR, Smileyscope’s FDA clearance is an important milestone for the industry. Smileyscope’s clearance represents not only the first FDA-cleared VR Analgesic for acute pain, but also the first clearance of a therapeutic VR system for the pediatric population.

“Smileyscope has now transformed over 100,000 procedures globally. Building on regulatory approvals in three other geographies, this confirms the strength of our data and the therapeutic power of our product,” said Dr. Paul Leong, Smileyscope’s Chief Marketing Officer and co-founder. “Smileyscope is the only VR device worldwide purpose-built for procedural support.”

“We were thrilled to receive this FDA Class II clearance. The FDA affirms Smileyscope’s long-held position that we are a transformational, therapeutic VR device, raising the standard of care,” said Dr. Evelyn Chan, CEO and co-founder of Smileyscope.

“We will build on this success. Our robust pipeline of drug-free pain and anxiety management treatments during common medical procedures spans children and adults. We look forward to the future where Smileyscope is in every hospital room, every doctor’s office, and every patient can benefit from our drug-free treatments,” said Chan.

“We are truly excited to receive FDA clearance. It is another recognition of our industry-leading status, along with best-in-class efficacy, best-in-class ease of use, and standard-elevating features like Procedural Choreography,” said Gavin West, VP of Sales and Marketing. “Results like this are what is driving the VR/XR and digital health spaces, making them amongst the fastest growing segments of healthcare.”

To learn more about Smileyscope, please visit www.smileyscope.com.

About Smileyscope:

Smileyscope is a multi-award-winning digital therapeutics company with proprietary technology that reframes medical procedures using choreographed virtual-reality (VR) experiences to help reduce patient pain and anxiety, improving patient experience and improving clinical workflows. Smileyscope Therapy is FDA-cleared for acute pain and anxiety reduction for needles procedures in children. Globally, Smileyscope has been utilized by clinicians across a range of medical procedures such as vaccines, bloodwork, wound dressings, anesthetic inductions, cast applications/removals, medical imaging and avoiding sedation. Smileyscope has partnered with over 50 US hospitals to implement the technology.

Disclaimer

Smileyscope, VR Analgesic and Procedural Choreography are registered trademarks of Smileyscope Holding Inc. The names and logos of third-party products and companies are the property of their respective owners and may also be trademarks. All trademarks, service marks and company names (e.g. AMA CPT®, UpToDate®) are the property of their respective owners.

References:

Digital Therapeutics Alliance, Understanding DTx, Accessed October 31 2023

Research and Markets, Digital Therapeutics Market Size, Share & Trends Analysis, 2023-2030, Accessed October 31 2023

Chan E, et al. Virtual Reality for Pediatric Needle Procedural Pain: Two Randomized Clinical Trials. The Journal of Pediatrics. 2019;209:160–7.

Gorski LA, et al. Infusion Therapy Standards of Practice, 8th Edition. Journal of Infusion Nursing. 2021;44(1S):S1–224.

Cravero JP, Roback MG. Procedural Sedation in Children: Approach. UpToDate, Accessed September 25 2023.

Media Contact

Cristy Brusoe, Smileyscope, 1 6518955842, [email protected], www.smileyscope.com 

SOURCE Smileyscope

American Canadian School of Medicine Receives welcomes 30 enthusiastic students from the Arthur Waldron SDA Academy


“ACSOM’s presence in Dominica is a new, transformative force. Our dedication to community, excellence, and student success is driving change that extends well beyond the classroom. The visit by students of Arthur Waldron SDA Academy is just one aspect of ACSOM’s overarching mission; which is to serve as a dynamic community partner, contributing to the enhancement of healthcare education and provision in Dominica.” said Dr. White.

The students were treated to immersive tours of ACSOM’s state-of-the-art facilities, including the Anatomy Lab and Simulation Lab. These hands-on experiences provided practical insights into medical training, supplementing knowledge beyond what textbooks alone can offer.

The collaboration between ACSOM and the Arthur Waldron SDA Academy extends beyond traditional education, embodying a shared vision of empowering the next generation of healthcare professionals, fostering dreams, and encouraging ambitious aspirations.

ACSOM’s presence in Dominica is a transformative force. The institution’s dedication to community, excellence, and student success is driving change that extends well beyond the classroom. The visit by Arthur Waldron SDA Academy students is just one aspect of ACSOM’s overarching mission to serve as a dynamic partner, contributing to the enhancement of healthcare standards in Dominica.

ACSOM has expressed its commitment to continue to be a valuable resource and partner to other local schools and leaders, reinforcing its dedication to advancing healthcare education accessibility across the region.

For more information about the American Canadian School of Medicine, its mission, and its ongoing efforts to elevate healthcare education and practice in Dominica, please visit ACSOM’s official website.

Media Contact

Elliot Polak, American Canadian School of Medicine, 8058891978, [email protected], www.acsom.edu.dm

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SOURCE American Canadian School of Medicine

Labroots Announces Agenda for its 14th Annual Clinical Diagnostics & Research Online Event


Over a decade of driving innovation with recognized experts and collaboration in clinical diagnostics and precision medicine

YORBA LINDA, Calif., Nov. 6, 2023 /PRNewswire-PRWeb/ — Labroots, the leading scientific social networking website offering premier, interactive virtual and hybrid events and webinars, today announced its 14th annual event in the Clinical Diagnostics & Research Virtual Event Series scheduled on November 8, 2023. This event will continue its long-standing commitment to advance clinical diagnostics, novel research and medicine, and to align research scholars, clinicians, top scientists, healthcare professionals and experts from leading academia and industry institutions under a virtual roof on a global basis.

For over a decade, this premier event serves as the premier educational catalyst for thought leaders dedicated to discussing emerging topics such as Emerging Diagnostic Technologies, Precision Medicine and Special Population, The Lab’s role in Advancing Equity, and Regulatory Compliance for Clinical Diagnostics.

At this year’s meeting, the jam-packed scientific agenda will highlight ground breaking advances covering the assay design and considerations in the development of lateral flow assays, the benefits of molecular diagnostic assay lyophilization, and important considerations in process development, benefits of real-time PCR Multiplexing, limitations of current TBI diagnostic methods in accurately characterizing and identifying TBI, interferences in lab assays by dietary supplements, the advantages of mass spectrometry in protein analysis, point of care testing for equitable access, the advantages and limitations of various methodologies used for paraproteinemia analysis, and more. Attendees will also see multiple panels and presentations from key industry sponsors including, Sartorius, Thermo Fisher Scientific, and Roche Diagnostics.

The opening keynote delivery titled, “Transforming the Clinical Lab through Equity, Inclusion, and Diversity” with a live Q&A session, will be presented by Dr. Linda Hasadsri, Director Molecular Technologies Laboratory, Chair of Equity, Inclusion, and Diversity, Department of Laboratory Medicine and Pathology at the Mayo Clinic. “The Department of Laboratory Medicine and Pathology at Mayo Clinic has adopted a number of creative and innovative approaches to addressing health disparities and supporting diversity in the workplace. I am thrilled that Labroots can serve as a platform to raise awareness of inequities in healthcare, particularly at the level of the clinical lab, and, better yet, be a vehicle for change. Together we can enhance the experiences of all people, all patients worldwide through equity, inclusion, and diversity in laboratory science,” stated Dr. Linda Hasadsri.

Labroots is a proud partner of Chati, a virtual event platform that allows for the hosting of engaging and interactive virtual and hybrid events, catering to businesses for any vertical or size. Hosted by Labroots and produced on Chati, participants in the event can connect seamlessly across desktop and mobile devices while engaged in a complete educational and interactive experience. Attendees will visit the lobby with leaderboard and gamification, an auditorium featuring live-streaming video webcasts with live attendee chats during scheduled presentations, an exhibit hall to interact with sponsors at their booths including ABSA International, Thermo Fisher Scientific, and Sino Biological highlighting their recent contributions in the field, a poster hall including a poster competition, live chat conversations, and a newly added Poster Networking Hour with live poster author meet and greets, and a networking lounge to encourage collaborations with colleagues. By attending this event, you can earn 1 P.A.C.E. Continuing Education credit per presentation for a maximum of 30 credits.

To register for the event click here. Use the hashtag #LRclinical to follow the conversation and connect with other members of the global Clinical & Molecular Dx Community!

Follow @Diagnostics_LR on Twitter and @ClinicalandMolecularDiagnostics.LR on Facebook to connect with our specialist Clinical & Molecular Dx Writers and stay up to date with the latest Trending News in Clinical & Molecular Dx. Join our Clinical & Molecular Dx Interest Group on LinkedIn to connect with us, and the wider professional community!

About Labroots
Labroots is the leading scientific social networking website, and primary source for scientific trending news and premier educational virtual events and webinars and more. Contributing to the advancement of science through content sharing capabilities, Labroots is a powerful advocate in amplifying global networks and communities. Founded in 2008, Labroots emphasizes digital innovation in scientific collaboration and learning. Offering more than articles and webcasts that go beyond the mundane and explore the latest discoveries in the world of science, Labroots users can stay atop their field by gaining continuing education credits from a wide range of topics through their participation in the webinars and virtual events. Now, Labroots offers more than ever with Chati, a flexible, highly scalable event platform that allows for the creation of unique, effective, and memorable virtual events.

Media Contact

Lynn Brainard, Labroots, 714-771-4397, [email protected], www.labroots.com

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SOURCE Labroots



Luniko Technologies Secures $700,000 in Non-Dilutive Pre-Seed Funding


Luniko Technologies Secures non-dilutive funding to develop cutting-edge products and services designed to accelerate an organization’s ability to adopt AI.

CALGARY, AB, Nov. 6, 2023 /PRNewswire-PRWeb/ — Luniko Technologies, a rapidly emerging technology firm, is thrilled to announce its acquisition of $700,000 in non-dilutive pre-seed funding. This capital injection will be directed towards the research and development of cutting-edge products and services designed to accelerate an organization’s ability to adopt AI.

Yassen Horanszky, CEO of Luniko, shared his excitement: “We envision a future where businesses can easily navigate the complexities of AI with confidence and clarity. With this investment, we are making significant strides towards actualizing this vision, and fulfilling our mission of enabling Canadian businesses to effectively integrate AI into their corporate DNA. The AI market is in its infancy, and our team will be delving deeper into identifying emerging trends and techniques that will define the future of AI adoption.”

As industries globally recognize the transformative power of AI, Luniko’s latest R&D initiatives aim to keep clients at the forefront of this technological evolution. By continuing to refine the “AI Readiness Gameplan,” Luniko ensures businesses possess both the knowledge and tools essential for effective AI integration.

For more information or to schedule an interview, contact: [email protected] 

About Luniko Technologies

Stationed at the heart of Calgary, Luniko Technologies is dedicated to assisting Canadian organizations incorporate AI into their operational framework. Recognizing that the first challenge with AI adoption is knowing where to start, Luniko leverages vast consulting experience on digital transformations to enable businesses by kickstarting their AI journey. Creating tailored AI gameplans to realize the edge that emerging technology can provide.

Media Contact

Alisa, Luniko, 1 4034047372, [email protected], www.lunikoconsulting.com 

SOURCE Luniko

Dr. Anna Chacon Continues Partnership With Exclusive Haute Beauty Network


Dr. Anna Chacon continues her partnership with Haute Beauty Network in her second year as a Skin Expert representing the Miami, FL market.

NEW YORK, Nov. 6, 2023 /PRNewswire-PRWeb/ — Dr. Anna Chacon is a board-certified dermatologist who has a passion for helping patients resolve their dermatologic conditions from the comfort of their homes. She grew up in Miami, Florida, and has lived in many different regions such as Chicago; Los Angeles, California; Providence, Rhode Island; Arctic Alaska; Cairo, Egypt; Haifa, Israel; and Buenos Aires, Argentina. She has a lifelong passion for being a doctor and physician, which was inspired by her father, Dr. Chacon, a pioneer in critical care in South Florida and founder of the largest private intensive care unit in the area. After frequently attending work with her father at the hospital, rounding and watching him care for others during natural disasters and times of need with a great sense of compassion, she knew from a young age that becoming a doctor was her calling and what she was born to do.

Alucio™ Adds Sage Therapeutics to Further Deepen Its Customer Base


Beacon will also compliantly enable MSLs to assemble custom presentations to meet the individual information needs of their Key Opinion Leaders (KOLs). Additionally, Beacon’s hybrid engagement functionality will provide unique, industry-specific features to enrich Sage’s virtual meetings across leading video conferencing platforms like Zoom and Teams. It will also power in-person meetings with HCPs using both tablets and laptops where data service is unavailable.

Beacon’s unifying scientific exchange workflow will seamlessly integrate into Sage’s broader enterprise CMS-CRM eco-system, providing Sage leadership with access to even more comprehensive content and engagement metrics for strategic decision making.

“Alucio’s Beacon platform will streamline and elevate our field based scientific exchange activities to help strengthen our relationships with HCPs”, said Colville Brown, Vice President – Global Medical Affairs Depression Franchise. “Beacon was developed specifically for medical affairs needs and provides us with the modern capabilities we were seeking to support our ambitious growth plans.”

Sage adds to Alucio’s fast-growing roster of life science companies that have become Beacon customers. The platform can support both large and small pharma, biotech, and medical device companies seeking to manage and distribute scientific content more efficiently and expand their relationships with both medical KOLs and payers.

“We are thrilled that Sage selected Beacon as part of their Medical Affairs and Field Medical vision”, said Jeff Asada, Co-Founder and Head of Customer Success at Alucio, “We look forward to supporting their growing commercialization success while ensuring that Sage’s field medical team can deepen KOL relationships as part of Sage’s omnichannel orchestration efforts.”

About Alucio:
Alucio is dedicated to the development of innovative software applications specifically for the life sciences industry. Alucio’s flagship product, Beacon, is a modern, cloud-based scientific exchange platform that enhances scientific dialogue and engagement between life science companies and healthcare professionals. For more information, please visit the company’s website at http://www.alucio.io or contact: Lisa Amin at [email protected] (925) 788-3533.

Media Contact

Lisa Amin, Alucio, 925-788-3533, [email protected], www.alucio.io

SOURCE Alucio