Rare Disease Day takes place worldwide, typically on or near the last day of February each year, to raise awareness among policymakers and the public about rare diseases and their impact on patients lives. Rare Disease Day at NIH 2023 Tuesday, February 28, 2023, 9:00am to 5:00pm (registration required) NIH Natcher Conference Center (Building 45) Rare Disease Day takes place worldwide, typically on or near the last day of February each year, to raise awareness among policymakers and the public about rare diseases and their Boston Dr. Gahl isthe Director of the Undiagnosed Diseases Program, a Senior Investigator in the Medical Genetics Branch and the Head of the Human Biochemical Genetics Section of the National Human Genome Research Institute (NHGRI). Most of these people are children. Suite 310 Hot off its heels we saw the accelerated approval of another bluebird bio product, Skysona. On Demand Content Available to Registered Attendees Until March 31, 2023. Crickresearchers are working at the forefront of the scientific response to answer some of the most urgent questions about the SARS-CoV-2 pathogen, from how we can improve testing, to why its deadly in some people but causes no symptoms in others. The goals of Rare Disease Day at NIH are to: Rare Disease Day at NIH was held at NIH Main Campus (Natcher Conference Center) on Tuesday, Feb. 28, 2023, from 9 a.m. to 5 p.m. EST. Connect and exchange with technology developers. Roscoe O. Brady Award Speaker: William A. Gahl, MD, PhD , Basic Science, Translational Research, ClinicalApplications, Contemporary Forum, and Late-Breaking Sessions, Emerging Trends: State-of the-Art for Experts, 2023 Scientific Sessions, ePosters and Satellite Symposia are available On Demand until. With a focus on the most critical topics, including accelerated approval, newborn screening, and equitable access to care, the 2023 NORD Summit promises a full program of productive discussions and collaborative solutions. The .gov means its official.Federal government websites often end in .gov or .mil. In all, nearly 10% of the U.S. population have a rare disease. February 13, 2023 Speaker and Abstract Submissions Open, March 10, 2023 Speaker Submission Deadline, March 15, 2023 Scholarship Application Window Opens, September 5, 2023 Early Bird Registration Closes, July 14, 2023 Abstract Submission Deadline, August 15, 2023 Abstract Decision Notifications by NORD, September 22, 2023 Hotel Room Block Closes, October 15, 2023 NORD Rare Diseases & Orphan Products Breakthrough Summit Welcome Reception, October 16 -17, 2023 NORD Rare Diseases & Orphan Products Breakthrough Summit, What an incredible lineup of speakers. The site is secure. Read more: https://bit.ly/3tGXzXn, Read the @RareDiseases Summit 2022 Recap! International Conference Rare Diseases and its Treatment aims to bring together leading academic scientists, researchers and research scholars to exchange and share their experiences and research results on all aspects of Rare Diseases . Jaguar Health to Present at BioTrinity 2023 Conferences R&D Spotlight on Rare Diseases - read this article along with other careers information, tips and advice on 2023 RARE Patient Advocacy Summit. Please enable JavaScript in your web browser to get the best experience. By RoundTables. The World Orphan Drug Congress brings together leading pharmaceutical and biotech companies, government and regulatory authorities, patient advocacy groups, payers, investors and solution providers. Youll have opportunities to learn quickly, advance your career, and to meaningfully impact our customers and our business. February 21, 2023: Robert J. Gorlin Symposium and Emerging Trends, Hilton Orlando6001 Destination ParkwayOrlando Florida, USA, 32819Phone: +1-407-313-4300Website: hilton.comWebsite: thehiltonorlando.com. WebRarediseases 2023 | 8th International Conference on Rare Diseases and Orphan Drugs 8 th International Conference on Rare Diseases and Orphan Drugs November 13-14, 2023 Osaka, Japan Submit Abstract Register Now Sessions & Tracks Program Schedule Reader Base Search 1000+ Events Join the National Organization for Rare Disorders (NORD) October 15-17, 2023 for the Rare Diseases and Orphan Products Breakthrough Summit. The Lysosomal Disease Network (U54NS065768) is a part of the National Institutes of Health (NIH) Rare Diseases Clinical Research Network (RDCRN), supported through collaboration between the NIH Office of Rare Diseases Research (ORDR) at the National Center for Advancing Translational Science (NCATS), the National Institute of Neurological Disorders and Stroke (NINDS) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). The World Orphan Drug Congress USA is a place where innovation and expertise is showcased, solutions are found and learning is done. NEMSNs Board had picked out six of them as particularly relevant to us. WebThe joint event RE(ACT) Congress and IRDiRC Conference 2023 aims to bring together scientific leaders and experts and young scientists from various breakthrough scientific fields to present cutting-edge research, exchange ideas, and discuss rare diseases research policies. Identify pertinent evolution of Health technologies in RARE DISEASES fields. (February 28, 2023) About Rare Disease Day Launched by EURORDIS-Rare Diseases Europe in 2008, Rare Disease Day is the patient-led international awareness campaign that brings people together in solidarity with the 300 million patients impacted Athanasios VOZIKIS, Professor, Director of LabHEM, University of Piraeus, Department of Economics 2022 has been a landmark year for the global gene therapy space. This years theme is Intersections with Rare Diseases A patient focused event. Participants will have the unique opportunity to: Public Docket We are a biomedical discoveryinstituteresearching the biologyunderlying human health. This website uses cookies to improve your experience. WORLDSymposium receives NO FUNDING of any kind from the LDN, the National Institutes of Health (NIH), or any other federal agency. Terrapinn is proud to be a member of isla. Summary. Rare Disease Day at NIH aims to raise awareness about rare diseases, the people they affect, and NIH collaborations that address scientific challenges and advance research for new treatments. WebThe joint event RE(ACT) Congress and IRDiRC Conference 2023 aims to bring together scientific leaders and experts and young scientists from various breakthrough scientific Read full announcement here. E:info@hansonwade.com, Sheraton Boston Hotel The theme for the conference this year is Bio Markers: Future of Medical Diagnosis and Treatment . Our primary method for achieving this is by creating exclusive business conferences that gather together the world's smartest thinkers and doers. November 18, 2022 Registration is now open for the 2023 Muscular Dystrophy Association (MDA) Clinical & Scientific Conference focusing on neuromuscular diseases, including Duchenne muscular dystrophy (DMD), spinal muscular atrophy (SMA), myasthenia gravis, and Pompe disease, among others. Join our mailing list to receive exclusive content and offers. WebRare Disease Conferences 2023 2024 2025 is for the researchers, scientists, scholars, engineers, academic, scientific and university practitioners to present research activities Discussions will focus on Each year, Global Genes convenes one of the worlds largest gatherings of rare disease patients, caregivers, advocates, healthcare professionals, Changing lives of those with rare disease. The 3rd International Conference on Rare Diseases organized by Rare Diseases Greece (RDG), 95 Rare Alliance Greece and Boussias, following the World Rare Disease Day 2023, will take place on [] Rare Diseases in the XXI Century Scientific Conference. Hanson Wade's goal is to accelerate progress within organisations and across industries. WORLDSymposium and the Lysosomal Disease Network (LDN) are separate and independent entities and are not affiliated in any way. NORD is a registered 501(c)(3) charity organization. ContactOOPDOrphanEvents@fda.hhs.gov | 301-796-7634 Location: Bartosza Gowackiego 35, Lublin, Poland. WebThe conference is a place to meet and brainstorm ways to advance orphan drug development and improve access to life-saving therapies. Conferences, and National Heart, Lung, and Blood Institute, National Institute on Alcohol Abuse and Alcoholism, National Institute of Neurological Disorders and Stroke, Rare Diseases Clinical Research Networks Coalition of Patient Advocacy Groups. After reviewing numerous nominations, and considering many amazing individuals, the WORLDSymposium 2023 Awards Committee has selected Christine as the recipient of the 2023 PAL Award. August 1, 2022Registration for the conference opens. wAIHA Warriors is providing travel , Continue reading "wAIHA Warriors Annual Patient Meeting", Since 2015, the Frank H. Netter MD School of Medicine at Quinnipiac University has hosted the Rare Disease Day Symposium, providing an opportunity for patients, family members, clinicians, and researchers to share their stories, research and insights into the development of novel therapeutics. The 6th Annual Gene Therapy for Rare Disorders 2023 Summit remains devoted to showcasing the top case studies and strategic learnings from the past year. Participants can join in on a virtual walk/run to raise awareness for Rare disease day (wearing stripes!). February 27 @ 9:00 am - 4:45 pm EST. 06885462, with its registered office at 1 Midland Road, London NW1 1AT. July 1, 2022Abstract submission website open. Phone: 617-249-7300, Danbury, CT office We are looking forward to gathering in person for Rare Disease Day 2023 on February 25th starting at 9:00 am at the Prince Conference Center (Grand The conference is a place to meet and brainstorm ways to advance orphan drug development and improve access to life-saving therapies. 15 16 Mar, 2023 Onsite & Online , Meet us at the World Rare Disease Day Conference in Medina, Saudi Arabia, on March 15-16, 2023 to learn more about how we work together with patients, physicians, and pharma partners to deliver data-driven, life-changing answers in rare and neurodegenerative diseases. Massachusetts Biotechnology Council 700 Technology Square, 5th Floor Cambridge, MA 02139 617.674.5100 By Facilitated Meetings. Attendees should look forward to coming together to celebrate five years of JHH successes and to build bridges to , Continue reading "Building Bridges to the Future: Jamals Helping Hands Anniversary BBQ", The Rare Disease Innovation & Partnership Summit, being held March 21-23 in Philadelphia, brings together experts from across the rare disease community to unite in areas of unmet medical need, create life-transforming therapies and breakthroughs, drive therapeutic progress, propel commercial strategies and inspire impactful advocacy. Presentation will cover Jaguar and Napo Therapeutics' focus on development and commercialization of WebMENA Organization for Rare Diseases and UAE Genetic Diseases Association will conduct the MENA Organization for Rare Diseases Annual Meeting 2023 in Dubai from 3 to 5 4 min read. People loved the speakers, the timely topics, the exhibit hall, and networking opportunities. Stakeholders are invited to provide their perspectives on the discussion questions through the public docket. Visit our exhibition on genome editing from 11 February 2023. Contribute to driving and directing the fast growing field of Health. WebKatie Wise - EveryLife Foundation for Rare Diseases | Rare Disease Conference 2023 - Rare Disease Innovation & Partnership Summit Speaker Agenda Speakers Sponsors & Exhibitors Contact Katie Wise Young Adult Rare Representative at EveryLife Foundation for Rare Diseases Profile Kaitlyn (Kate) Wise grew up in Westchester, NY. Demonstrate the NIH commitment to helping people with rare diseases through research. The Francis Crick Institute1 Midland RoadLondon NW1 1AT, View upcoming changes to normal opening times. Explore a selection of reports that spotlight particular areas of research at the Crick over the past five years. By continuing to use this website, you agree to the Terms of Service & Privacy Policy, A Podcast For The Rare Disease Community, Policy Statements & Letters to Policymakers. This years How do lay professionals deal with issues around gender and sexuality in the community? Download the presentation, International Conference on Rare Diseases 2023, Leveraging the momentum for a comprehensive rare disease strategy. The Francis Crick Institute Limited is a registered charity in England and Wales no. Engage with the FDA to provide your perspectives as a patient, caregiver or family member. Rare Disease Therapies Development IL, Virtual Summit. Appraise and qualify unmet needs from clinician users. How are you raising awareness for the rare community this Rare Disease Day? How are you raising awareness for the rare community this Rare Disease Day? All are welcome to join the celebration to cheer on our skaters. Our mission is to promote inter-professional healthcare education and awareness of and , Continue reading "2023 Rare Disease Day Symposium at the Frank H. Netter MD School of Medicine", 1900 Crown Colony Drive Applications for the 2023 PhD programme are open! The conference will start at approximately 13:00 on Monday 24 April 2023 and close at approximately 14:30 on Wednesday 26 April 2023. Understand considerations and challenges associated with clinical trials in small populations. With August came the green light for, As the gene therapy field continues to break records, there are still significant challenges to overcome relating to safety, efficacy, and accessibility. Learn more about how you can attend this event or add it to your calendar. FDA will host Rare Disease Day, a virtual public meeting, on February 27, 2023, 9:00 am 4:45 pm ET, in global observance of Rare Disease Week. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Quincy, MA 02169 The 2023 virtual event is hosted in partnership between CHOC and UCI, together, we will foster new perspectives, ideas, and research collaborations to accelerate , Continue reading "The 2nd Annual CHOC and UCI Rare Disease Symposium & Family Conference", NORD Wisconsin Rare Action Network Rare Disease Day Saturday, March 11, 2023 Evjue Commons space at Olbrich Botanical Gardens 3330 Atwood Ave, Madison, WI 53704 Event is from 1:00pm -3:00 pm There is no cost to participants to attend this event One of the greatest challenges individuals living with a rare disease, their families, and , Continue reading "Wisconsin Rare Disease Day", NORD Iowa Rare Action Network Rare Disease Day Saturday, March 11, 2023 This is a virtual event. Read full announcement here. Join us for three days in Broadly acclaimed speakers, the most recent frameworks, methodologies, and the most current updates in this field are indications of this conference. NORD, along with its more than 300 patient organization members, is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and patient services. October 15-17, 2023 Join our mailing lists to receive updates about our latest research and to hear about our free public events and exhibitions. WORLDSymposium is managed by GMI, Inc. and Saterdalen & Associates, LLC. Congratulations to this years recipients! Join the webcast to watch the livestream on February 27 beginning at 9 a.m. (ET). Exchange the latest rare diseases information with stakeholders to advance research and therapeutic efforts. Phone: 203-263-9938 How are you raising awareness for the rare community this Rare Disease Day? Google Calendar iCalendar Outlook 365 Outlook Live Details Date: February 27 Time: 9:00 am - 4:45 pm EST Event Category: NORD Sponsored Rare Disease Day Event Website: November 15, 2022Notification of abstract acceptance for poster or platform presentation at WORLDSymposium 2023. Translate technological capabilities into clinical applications, relevant to daily practice. By submitting, you agree to receive email communications from Terrapinn, including upcoming promotions and discounted tickets and news. Third International Summit on Human Genome Editing Previous Events; Today Next Events; 1st International UAE Rare Disease Society Congress Feb 28 February 28 - March 1. WebMarketsandMarkets Infectious Disease and Molecular Diagnostics Conference 22nd - 23rd June 2023 Boston, USA The Diagnostics sector has emerged as a prominent game changer in healthcare, because of many technological advancements taking WORLDSymposiumwas pleased to announce the recipients of the 2023 Young Investigator Award. All Info for H.Res.181 - 118th Congress (2023-2024): Expressing support for the designation of February 28, 2023, as "Rare Disease Day". (February 28, 2023) About Rare Disease Day Launched by EURORDIS-Rare Diseases Europe in 2008, Rare Disease Day is the patient-led international awareness campaign that brings people together in solidarity with the 300 million patients impacted This conference is aimed at scientists, clinician scientists and doctors. Fax: 203-263-9938, Washington, DC Office Webcast Information Overseas, July and August brought EMA approvals for PTC Therapeutics'Upstaza and BioMarins Roctavian, the first gene therapies for AADC deficiency and Haemophilia A respectively. Hear from medical students on rare disease education for medical professionals. View CNBC interview with NORDs Peter Saltonstall and Boston Childrens Dr. Olaf Bodamer emphasizing the importance of investment in rare diseases. Sessions will include information from patients, physicians, and researchers regarding wAIHA clinical trials, current treatments, access to care, federal and state advocacy efforts, etc. Summary WebClinical Trials in Rare Diseases 2023 We are pleased to announce the launch of a brand new event: Clinical Trials in Rare Diseases will take place on 13th-14th September 2023 in Princeton! Stay Informed With NORDs Email Newsletter, "Skate Under the Stars: A Rare Disease Celebration", "2023 Illinois Rare Disease Day at the Capital", "The 2nd Annual CHOC and UCI Rare Disease Symposium & Family Conference", "Building Bridges to the Future: Jamals Helping Hands Anniversary BBQ", "Rare Disease Innovation & Partnership Summit", Renaissance New Orleans Pere Marquette French Quarter, "2023 Rare Disease Day Symposium at the Frank H. Netter MD School of Medicine", Launching Registries & Natural History Studies, Skate Under the Stars: A Rare Disease Celebration, CHOC Rare Disease Grand Rounds: Pyridoxine Dependent Epilepsy (PDE), 2023 Illinois Rare Disease Day at the Capital, The 2nd Annual CHOC and UCI Rare Disease Symposium & Family Conference, Building Bridges to the Future: Jamals Helping Hands Anniversary BBQ, Rare Disease Innovation & Partnership Summit, 2023 Rare Disease Day Symposium at the Frank H. Netter MD School of Medicine. Office of Clinical Policy and Programs, Office of Orphan Products Development, More Meetings, Working together to build sustainable events, Multiple Myeloma Research Foundation (MMRF), anti-money laundering & financial crime policy. The goal of WORLDSymposium is to provide an interdisciplinary forum to explore and discuss specific areas of interest, research and clinical applicability related to lysosomal diseases. Suite 500 Even after an accurate diagnosis, treatment often is not available because fewer than 500 rare diseases have FDA-approved treatments. T: (+1) 617 455 4188 WebWorld Rare Disease Day Conference 2023. Registration is required. Download the presentation, Magda CHLEBUS, Executive Director, Science Policy & Regulatory Affairs At EFPIA WebRare Disease Conference 2023 - Rare Disease Innovation & Partnership Summit informaconnect.com Each year, WORLDSymposium hosts a scientific meeting presenting the latest information from basic science, translational research, and clinical trials for lysosomal diseases. This years theme is Intersections with Rare Diseases A patient focused event.. Rare Disease Day at NIH will be held in person at NIH Main Campus (Natcher Conference Center) on Tuesday, Feb. 28, 2023, from 9 a.m. to 5 p.m. WORLDSymposium is a medical education conference focused on lysosomal diseases. 55 Kenosia Avenue WebThe joint event RE(ACT) Congress and IRDiRC Conference 2023 aims to bring together scientific leaders and experts and young scientists from various breakthrough scientific fields to present cutting-edge research, exchange ideas, and discuss rare diseases research policies. Join us for three days in Washington for the most comprehensive program and inclusive gathering of rare disease stakeholders. THE BENEFITS PROVIDED TO THE ATTENDEES ARE: PARTICIPANTS - FIVE REASONS WHY I SHOULD ATTEND THE CONGRESS: PARTNERS - REASONS WHY I SHOULD EXHIBIT DURING THE CONGRESS: Copyright All rights reserved | Design & Developed by, Re-conceptualizing existing paradigms of diagnosis and difficulty, Breaking down silos how different models fit together. Event Details. Shine a spotlight on stories told by people living with a rare disease, their families and their communities. 3RD INTERNATIONAL RARE DISEASES CONFERENCE 2023: Expert speakers from across the UK Rare Diseases community will present their latest research. A global community in the heart of London. WORLDSymposiumwas pleased to announce the recipients of the 2023 New Treatment Award. NORD at UVA Speaker Panel 2023 . We invite you to join us for the 14th Annual Conference on Advancing Rare Disease Research, Therapy, and Patient Advocacy on March 3-4, 2023 in the Jordan Research led by NCATS suggests that nationwide medical costs for individuals with rare diseases are likely as high as those faced by people with common diseases, such as cancer and heart failure. The conference is specifically for patients and caregivers. WebVideo: Rare Disease Day Conference 2023 | Akron Children's Hospital. NORD, a 501(c)(3) organization, is a patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them. On October 17 and 18, the National Organization for Rare Disorders (NORD) hosted the Rare Diseases and Orphan Products Breakthrough Summit. Rare Disease Conferences 2023/2024/2025 lists relevant events for national/international researchers, scientists, scholars, professionals, engineers, exhibitors, sponsors, academic, scientific and university practitioners to attend and present their research activities. http://ow.ly/5Wzs50Lj6CJ #NORDSummit. Rare diseases often are difficult to diagnose it can take years. From: 09/19/2023 To: 09/20/2023. Learn more about how you can attend this event or add it to your calendar. Christines work at Cure GM1 has involved a broad range, including animal models, biomarkers, gene therapy, enzyme replacement therapy, patient registries, patient reported outcomes, newborn screening and the first-ever GM1 caregiver preferences study. Google Calendar. Click here to access the Guide for Authors or to Submit Your Paper. This will be an in-person meeting only. NCATS is committed to using research to address the public health crisis presented by rare diseases. Click here to access the Guide for Authors or to Submit Your Paper. Volunteer. 13 - 14 September 2023 Princeton, New Jersey Register Why attend? The WORLD CONGRESS ON RARE DISEASES - 2023, - An International Conference by BioGenesis Health Cluster is among the Worlds leading RARE DISEASE Conferences. Copyright 2023 NORD National Organization for Rare Disorders, Inc. All rights reserved. It also provides a premier interdisciplinary platform for researchers, practitioners and educators to present and discuss the most recent innovations, trends, and concerns as well as practical challenges encountered and solutions adopted in the fields of Rare Diseases. Each year, WORLDSymposiumrecognizes one individual for innovation and accomplishment in the field of lysosomal disease research and therapy. Washington, DC 20036 NORD is not a medical provider or health care facility and thus can neither diagnose any disease or disorder nor endorse or recommend any specific medical treatments. Download the presentation, Antonis KATTAMIS, Professor of Pediatric Hematology-Oncology, President, Hellenic Society of Pediatric Hematology-Oncology The virtual approach cant replace in-person conversations, but can reach people and enable important connections. WebInternational Conference on Rare Diseases 2023. 39 Dalton St, If you have problems viewing PDF files, download the latest version of Adobe Reader, For language access assistance, contact the NCATS Public Information Officer, National Center for Advancing Translational Sciences (NCATS), 6701 Democracy Boulevard, Bethesda MD 20892-4874 301-594-8966, U.S. Department of Health & Human Services, Clinical and Translational Science Awards (CTSA) Program, Rare Diseases Clinical Research Network (RDCRN), Therapeutics for Rare and Neglected Diseases (TRND), Additional Rare Diseases Research and Initiatives, Patient/Community Engagement & Health Information, Genetic and Rare Diseases Information Center, NCATS Toolkit for Patient-Focused Therapy Development, National COVID Cohort Collaborative (N3C), About NCATS Role in the NIH HEAL Initiative, Accelerating the Translation of Novel Compounds Toward INDs for Subsequent Clinical Testing, Fiscal Year 2019 Funded Projects and Prizes, NIH HEAL Initiative Funding & Collaboration Opportunities Led by NCATS, NCATS Program-Specific Funding Information, Prior NIH Approval of Human Subjects Research Frequently Asked Questions, NCATS Challenges and Prize Competitions Program, Bias Detection Tools in Health Care Challenge, LitCoin Natural Language Processing (NLP) Challenge, NCATS Rare Diseases Are Not Rare! Leveraging the momentum for a comprehensive rare disease strategy Introductory Speech: An Session: R&D Spotlight - Rare Disease Date: Tuesday, April 25, 2023 Time: 4:00 p.m. - 5:15 p.m. Greenwich Mean Time Venue: ETC Venues, 155 Bishopsgate, London, England EC2M 3YD About BioTrinity BioTrinity is a London conference that catalyzes growth and supports in-person re-engagement across the life sciences industry. Sheraton Harbor Island, 1380 Harbor Island Dr, San Diego, CA 92101. iBIO invites you to join patients, families, caregivers and other rare disease community members at this important event to educate Illinois legislators and the general public on the challenges faced by rare disease patients and their families. WebWorld Congress on Rare Diseases - 2023 +91 83102 90512 info@worldcongressonrarediseases.com About Conference The International Research Receive updates on the NORD Summits agenda, speakers, registration, and more by opting into our mailing list. All comments must be identified with the docket number FDA-2022-N-3072-0001 through April 7, 2023. 1140062 and a company registered in England and Wales no. 08:00 AM 05:00 PM UTC-12:00. WORLDSymposium is an annual research conference dedicated to lysosomal diseases. This exciting event brings together over 900 rare disease advocates, experts, and stakeholders from around the world to tackle the most pressing issues facing the rare disease community. Read full announcement here. WebRare Disease Day will be taking place on March 24, 2023 at 5:00 PM (ET). The. Led by 60+ expert speakers and together with your peers, , Continue reading "Rare Disease Innovation & Partnership Summit", The first ever wAIHA Warriors Annual Patient Meeting will take place from March 24-26, 2023, in New Orleans. Rare Disease conference listings are indexed in scientific databases like Google Scholar, Semantic Scholar, Zenedo, OpenAIRE, EBSCO, BASE, WorldCAT, Sherpa/RoMEO, Compendex, Elsevier, Scopus, Thomson Reuters (Web of Science), RCSI Library, UGC Approved Journals, ACM, CAS, ACTA, CASSI, ISI, SCI, ESCI, SCIE, Springer, Wiley, Taylor Francis, and The Science Citation Index (SCI).

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