On Demand Content Available to Registered Attendees Until March 31, 2023. Event Details. Join our mailing lists to receive updates about our latest research and to hear about our free public events and exhibitions. WebRare Diseases Meet 2023 provides a premier interdisciplinary platform for researchers to present the latest research findings and describe emerging technologies, and directions in rare diseases and orphan drugs issues. Planning committee members included representatives from the following organizations: Progress in data science and an increased understanding of disease genetics lead experts to agree that more than an estimated 10,000 rare diseases are affecting about 30 million people in the United States. Engage with the FDA to provide your perspectives as a patient, caregiver or family member. If you would like to find out more about how we manage your personal information please see our privacy policy. Each year, WORLDSymposiumrecognizes one individual for innovation and accomplishment in the field of lysosomal disease research and therapy. Download the presentation, International Conference on Rare Diseases 2023, Leveraging the momentum for a comprehensive rare disease strategy. Stakeholders are invited to provide their perspectives on the discussion questions through the public docket. Join us virtually or in-person on March 10 for the 10th Annual Rare Disease Symposium. Marriott Marquis in Washington, DC, NORD Leads the Way: 900+ Influential Rare Disease Stakeholders from FDA, Patient Organizations, and Industry Gather for #NORDSummit 2023. The site is secure. Congratulations to this years recipients! Receive updates on the NORD Summits agenda, speakers, registration, and more by opting into our mailing list. Connect, exchange with clinicians and health policy makers. 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. NEMSNs Board had picked out six of them as particularly relevant to us. 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. 1779 Massachusetts Avenue WORLDSymposium receives NO FUNDING of any kind from the LDN, the National Institutes of Health (NIH), or any other federal agency. The World Orphan Drug Congress USA is a place where innovation and expertise is showcased, solutions are found and learning is done. WebGT+R 2023 is a novel event, curating seasoned experts from across the gene therapy and rare disease therapeutic research and development industries. Read full announcement here. Each year, Global Genes convenes one of the worlds largest gatherings of rare disease patients, caregivers, advocates, healthcare professionals, Your meeting registration confirmation will include a link to generate a customized letter of invitation, which can be used when applying for a visa. 39 Dalton St, Christine founded the Cure GM1 Foundation in April 2015 in honor of her daughter Iris and all those affected by GM1 gangliosidosis. Join the webcast to watch the livestream on February 27 beginning at 9 a.m. (ET). FDA Meetings, Conferences and Workshops, Recalls, Market Withdrawals and Safety Alerts, FDA Meetings, Conferences, and Workshops: Past Events, Public Calendar - Meetings With FDA Officials, Public meeting: FDA Rare Disease Day 2023 - 02/27/2023, RDD 2023 Meeting Packet Brochure 02-02-2023_final_508. Keep up-to-date on the latest NORD Summit news, Director of Development and Strategic Partnerships, The Myositis Association, Lois Vierk, President, National Eosinophilia Myalgia Syndrome Network, Susan Fernbach, RN, Director of Genetic Outreach, Baylor College of Medicine and member of NORDs Summit Advisory Committee. Sessions will include information from patients, physicians, and researchers regarding wAIHA clinical trials, current treatments, access to care, federal and state advocacy efforts, etc. Challenges faced by lay professionals in the community, Certificates will be provided to all speakers, delegates and students, Opportunity to meet worlds renowned at this event, Keynote forums by Prominent Physicians & Professors, Best platform for Global business and networking opportunities, Oral/Poster presentations by Young Researchers. This will be an in-person meeting only. Speakers Sponsors Media Centre Contact Us Register close 2023 Sponsors Included: Why attend? Summary. Our primary method for achieving this is by creating exclusive business conferences that gather together the world's smartest thinkers and doers. MA 02199 WebRare Disease Day will be taking place on March 24, 2023 at 5:00 PM (ET). Youll have opportunities to learn quickly, advance your career, and to meaningfully impact our customers and our business. Thank you for the opportunity to present on the vitally important topic of transition of care., NEMSNs Board thanks you very kindly for your scholarship to our organization to attend the 2020 Rare Summit. The WORLD CONGRESS ON RARE DISEASES - 2023, - An International Conference by BioGenesis Health Cluster is among the Worlds leading RARE DISEASE Conferences. 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. Rare Disease Therapies Development IL, Virtual Summit. How are you raising awareness for the rare community this Rare Disease Day? 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 Click here to access the Guide for Authors or to Submit Your Paper. WebRare Disease Conferences 2023 2024 2025 is for the researchers, scientists, scholars, engineers, academic, scientific and university practitioners to present research activities 2020 Challenge Details, Translational Science Education & Training, Translational Science Training at Partner Institutions, Translational Science Training and Education Resources, Drug Discovery, Development and Deployment Maps, Assay Development and Screening Technology (ADST), Bridging Interventional Development Gaps (BrIDGs), Discovering New Therapeutic Uses for Existing Molecules, Genetic and Rare Diseases Information Center (GARD), A Specialized Platform for Innovative Research Exploration (ASPIRE), A Translational Approach to Addressing COVID-19, Clinical Trial Readiness for Rare Diseases, Disorders and Syndromes, Multidisciplinary Machine-Assisted, Genomic Analysis and Clinical Approaches to Shortening the Rare Diseases Diagnostic Odyssey, The Accelerating Medicines Partnership Bespoke Gene Therapy Consortium (BGTC), Cures Acceleration Network (CAN) Review Board, Division of Rare Diseases Research Innovation (DRDRI), access shareable resources to help raise awareness about rare diseases. WORLDSymposium is a medical education conference focused on lysosomal diseases. Broadly acclaimed speakers, the most recent frameworks, methodologies, and the most current updates in this field are indications of this conference. 4 min read. Location: Bartosza Gowackiego 35, Lublin, Poland. WebRare Disease Day will be taking place on March 24, 2023 at 5:00 PM (ET). Before sharing sensitive information, make sure you're on a federal government site. Explore a selection of reports that spotlight particular areas of research at the Crick over the past five years. Applications for the 2023 PhD programme are open! 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. http://ow.ly/5Wzs50Lj6CJ #NORDSummit. WebThe 2023 Gordon Research conference on Lysosomal Diseases will cover the latest discoveries that advance knowledge about basic lysosomal function; how exactly function is impaired in lysosomal diseases - and how they inform more universal application in How do lay professionals deal with issues around gender and sexuality in the community? 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. Phone: 202-588-5700. The conference will start at approximately 13:00 on Monday 24 April 2023 and close at approximately 14:30 on Wednesday 26 April 2023. This will coordinate appears, disperse information, and meet with recurring pattern and potential investigators and get name affirmation at First Virtual Conference. Information on how to claim education credits is given only to registered attendees and is available in the 2023 WORLDSymposium mobile app. So you can: Exchange ideas, Build brand, Form friendships and partnerships, Grow your professional network, Explore the future, Uncover new opportunities., ADVANCED THERAPIES - CLINICAL DEVELOPMENT. 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). WORLDSymposium is excited to announce the return of Peter Marks, MD, PhD, director of the Center for Biologics Evaluation and Research (CBER) at the Food and Drug Administration, as the 2023 Keynote Speaker. 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. NORD at UVA Speaker Panel 2023 . 06885462, with its registered office at 1 Midland Road, London NW1 1AT. Dr. Marks Keynote Address: Taking Gene Therapy to the Next Level, was presented on Friday, February 24, 2023 at 7:30 AM EST, at the 19th Annual WORLDSymposium in Orlando, Florida. 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. WebLeveraging the momentum for a comprehensive rare disease strategy The 3rd International Conference on Rare Diseases organized by Rare Diseases Greece (RDG), 95 Rare WebThe Second Annual CHOC and UCI Rare Disease Symposium & Family Conference will bring together over 100 advocates, researchers, clinicians, students, and families to Registration is required. 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 In all, nearly 10% of the U.S. population have a rare disease. 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. This exciting Google This year conference will comprises of major sessions designed to offer comprehensive sessions that address current issues in various field of RARE DISEASES. Over 830 enthusiastic attendees from across the globe convened to address and take action on the opportunities and challenges facing the rare disease community. Working together to build sustainable events, Multiple Myeloma Research Foundation (MMRF), anti-money laundering & financial crime policy. Presentation will cover Jaguar and Napo Therapeutics' focus on development and commercialization of February 27 @ 9:00 am - 4:45 pm EST. Download the presentation, Panagiota MITROU, Deputy Head of the Autonomous Department of Therapeutic Protocols & Patient Registries, Ministry of Health Click here to access the Guide for Authors or to Submit Your Paper. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. 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. 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. February 21, 2023: Robert J. Gorlin Symposium and Emerging Trends February 22-26, 2023: Research Meeting Hilton Orlando, Orlando, FL, USA Scientific Web3RD INTERNATIONAL RARE DISEASES CONFERENCE 2023: GREEK CHAPTER Mar 6 March 6 - March 8. Assess and understand application challenges with current technology features. 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. E:info@hansonwade.com, Sheraton Boston Hotel This years theme is Intersections with Rare Diseases A patient focused event.. Even after an accurate diagnosis, treatment often is not available because fewer than 500 rare diseases have FDA-approved treatments. Join the webcast to watch the livestream on February 27 beginning at 9 a.m. (ET). 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. Davide Zecchin and Sara Barbera Martin (Senior Post-Doctoral Research Associates, Kinsler lab, Francis Crick Institute), Prof Rob Semple, Professor of Translational Molecular Medicine, University of Edinburgh, What causes insulin resistance, and what can we do about it?, Prof Steve Hart, Professor in Molecular Genetics, UCL, Dr Helen Brittain, Clinical Lead for Rare Disease Diagnostics, Genomics England, "The 100,000 Genomes Project and beyond: An update on Rare Disease Diagnosis and Research", Prof Sergi Castellano, Professor of Genomics, UCL, Prof Hannah Mitchison, Professor of Molecular Medicine, UCL, "Rare genetic respiratory diseases and targeting genetic therapies to the airways", Prof Alan Warren, Professor of Haematology, University of Cambridge, "Convergent somatic evolution commences in utero in a germline ribosomopathy", Prof Veronica Kinsler, Professor of Paediatric Dermatology and Dermatogenetics, GOSH, UCL and the Francis Crick Institute, Maanasa Polubothu (clinical academic PI, UCL and consultant Great Ormond St) and Dale Bryant (senior post-doctoral research associates, Kinsler lab, Francis Crick Institute), Dr Antoine de Fougerolles, CEO Evox Therapeutics, "Exosome therapeutics: creating and enabling genetic medicines", Prof Mina Ryten, Professor of Clinical Genetics, GOSH and UCL, "Leveraging transcriptomics to understand rare genetic diseases of the human brain", Prof Siddharth Banka, Professor of Genomic Medicine and Rare Diseases, University of Manchester, "Mechanistic and clinical heterogeneity of single gene disorders illustrated by non-muscle actinopathies", Prof Paul Gissen, Professor of Paediatric Metabolic Diseases, GOSH and UCL, "Towards understanding a rare membrane trafficking disorder ARC", Prof Mariya Moosajee, Professor of Molecular Ophthalmology, Moorfields, UCL and the Francis Crick Institute, "Choroideremia - is it just a rare eye disease? By App. Massachusetts Biotechnology Council 700 Technology Square, 5th Floor Cambridge, MA 02139 617.674.5100 Hear from medical students on rare disease education for medical professionals. October 15-17, 2023 All attendees who registered for On Demand will receive an email with a link to access the On Demand platform starting Monday, February 27 until Friday, March 31, 2023. Most of these people are children. 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. By RoundTables. Rare Disease Conferences 2023/2024/2025 is an indexed listing of upcoming meetings, seminars, congresses, workshops, programs, continuing CME courses, trainings, summits, and weekly, annual or monthly symposiums. ContactOOPDOrphanEvents@fda.hhs.gov | 301-796-7634 The event agenda featured panel discussions, rare diseases stories, exhibitors and scientific posters. Advancing Rare Disease Research with Patient Centrality and Precompetitive Approaches- Screen4Care as a Case. Rare diseases often are difficult to diagnose it can take years. Download the presentation, Magda CHLEBUS, Executive Director, Science Policy & Regulatory Affairs At EFPIA WebRare Disease Day will be taking place on March 24, 2023 at 5:00 PM (ET). Join us for three days in Annual Summit on Rare Diseases and Orphan Drugs, International Conference on Rare Infectious Diseases (ICRID), International Conference on Rare Diseases and Indigenous Genetics (ICRDIG), International Conference on Orphan Drugs for Rare Diseases (ICODRD), International Conference on Clinical Genetics and Rare Diseases (ICCGRD), International Conference on Orphan Drugs, Rare Diseases and Conditions (ICODRDC), International Conference on Orphan Drugs and Rare Diseases (ICODRD), International Conference on Rare Diseases and Orphan Drugs (ICRDOD), Creative Commons Attribution 4.0 International license. Dr.Marks gave presentations to the WORLDSymposium audience in 2020 and 2021, providing important updates on the FDAs role in rare disease research, and he presented the 2023 Keynote Address on Friday, February 24, 2023. United States. 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). Sheraton Harbor Island, 1380 Harbor Island Dr, San Diego, CA 92101. Illinois Rare Disease Day at the capital brings together rare disease advocates from across the state to make , Continue reading "2023 Illinois Rare Disease Day at the Capital". 1140062 and a company registered in England and Wales no. 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. Join us for a celebration of Rare Disease Day with an opportunity for Rare Disease Warriors to Skate Under the Stars at the Centene Community Ice Center outdoor rink in Maryland Heights, MO. Translate technological capabilities into clinical applications, relevant to daily practice. 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. Read full announcement here. Thank you for the well-organized machinery that allowed us opportunities to arrange meetings. Hear directly from the FDA on initiatives to advance medical product development for rare diseases. Congratulations to Christine Waggoner, the recipient of the WORLDSymposium 2023 Patient Advocate Leader (PAL) Award. Changing lives of those with rare disease. Connect and exchange with technology developers. WORLD is an acronym that stands for Were Organizing Research on Lysosomal Diseases. NCATS is committed to using research to address the public health crisis presented by rare diseases. 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. Download the presentation, Mari MUREL, ERICA Project Manager Read full announcement here. Brain Injury Alliance of Webcast Information Learn more about how you can attend this event or add it to your calendar. Events will run over a span of time during the conference depending on the number and length of the presentations. View CNBC interview with NORDs Peter Saltonstall and Boston Childrens Dr. Olaf Bodamer emphasizing the importance of investment in rare diseases. Learn more about how you can attend this event or add it to your calendar. November 15, 2022Notification of abstract acceptance for poster or platform presentation at WORLDSymposium 2023. About Rare Disease Day . 2022 has been a landmark year for the global gene therapy space. This free family-friendly BBQ will feature live music, a kid's zone, food trucks, educational resources, and more! Phone: 617-249-7300, Danbury, CT office 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. Overview, new treatments, and the potential for Newborn Screening for Pyridoxine Dependent Epilepsy (PDE) Speaker: Curtis R. Coughlin II, PhD, MS, MBE CHOC Grand Rounds is part of the CHOC UCI Rare Disease Day. 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. By Hangin Out. 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. Featuring content on the most critical rare issues including accelerated approval, newborn screening, equitable access to care the 2022 NORD Summit was host to a week of conversations and collaborations in the global community. Demonstrate the NIH commitment to helping people with rare diseases through research. October 1, 2022Deadline for submission of full-length manuscripts for peer-review in the Lysosomes issue of Molecular Genetics & Metabolism, February, 2023. How are you raising awareness for the rare community this Rare Disease Day? With August came the green light for bluebird bios Zynteglo in the US, the first FDA approval for a gene therapy in over three years. The International Research Conference Aims and Objectives. WORLDSymposium and the Lysosomal Disease Network (LDN) are separate and independent entities and are not affiliated in any way. Present and discuss your plans, activities and products. Shine a spotlight on stories told by people living with a rare disease, their families and their communities. WebWelcome The BLACKSWAN Foundation and IRDiRC, the International Rare Diseases Research Consortium, will host the joint in-person event RE(ACT) Congress and IRDiRC 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. Workshops, Public meeting: FDA Rare Disease Day 2023, An official website of the United States government, : 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. WebInternational Conference on Rare Diseases 2023. WebConference Series LLC Ltd welcomes you to attend the Biomarkers, Cancer Therapy & Clinical Research Conference to be held in Vancouver, Canada on September 23-24, 2023. Vice President, Discovery and Translational Research. 13 - 14 September 2023 Princeton, New Jersey Register Why attend? Identify pertinent evolution of Health technologies in RARE DISEASES fields. Event is from 2:00pm -4:00 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 patient advocates have is finding and accessing information , Join the Jamals Helping Hands (JHH) five-year anniversary, Building Bridges to the Future, honoring their community, resilience, and strength. Presentations. This years conference will include presentations on next generation technology, long-read genome sequencing, patient empowerment and health equity, and more. 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. Join the National Organization for Rare Disorders (NORD) October 15-17, 2023 for the Rare Diseases and Orphan Products Breakthrough Summit. 2nd Crick Rare Diseases Conference | Crick 28 February 2023 09:00 - 17:00 The Francis Crick Institute Symposia Register on Eventbrite What's on Expert As the gene therapy field continues to break records, there are still significant challenges to overcome relating to safety, efficacy, and accessibility. Get your product or solution in front of the leaders in the rare disease industry from pharma, biotechs, governments, payers, investors and patient/patient advocates. We are always looking for ambitious people to join our team. Expert speakers from across the UK Rare Diseases community will present their latest research. 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. On October 17 and 18, the National Organization for Rare Disorders (NORD) hosted the Rare Diseases and Orphan Products Breakthrough Summit. Join our mailing list to receive exclusive content and offers. Leveraging the momentum for a comprehensive rare disease strategy Introductory Speech: An 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. We have kicked off 2023 with our continued support of Medics4RareDiseases (M4RD) during their annual symposium, and today, the emotive Visit our exhibition on genome editing from 11 February 2023. 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. WebThe conference is a place to meet and brainstorm ways to advance orphan drug development and improve access to life-saving therapies. Fax: 203-263-9938, Washington, DC Office Web8th International Conference on Rare Diseases and Orphan Drugs Osaka, Japan November 13-14, 2023 6th International Conference on Tropical and Infectious Diseases Bali, Indonesia December 07-08, 2023 6th Pathology and Infectious Disease Conference Prague, Czech Republic December 14-15, 2023 13th European Epidemiology and Public
