Meet Inspiring Speakers and Experts at our 3000+ Global Events with over 1000+ Conferences, 1000+ Symposiums and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World’s leading Event Organizer

Conference Series Conferences gaining more Readers and Visitors

Conference Series Web Metrics at a Glance

  • 3000+ Global Events
  • 100 Million+ Visitors
  • 75000+ Unique visitors per conference
  • 100000+ Page views for every individual conference

Unique Opportunity! Online visibility to the Speakers and Experts

Renowned Speakers

David R. Schoneker

David R. Schoneker

President/Owner/Consultant, USA

Vladimir Matveevich Gruznov

Vladimir Matveevich Gruznov

Professor Russian Academy of Sciences, Russia Russia

Oleg Shpigun

Oleg Shpigun

Professor Lomonosov Moscow State University, Russia

Gilles Goetz

Gilles Goetz

Principal Scientist Pfizer, USA

Haifei Zhang

Haifei Zhang

Doctor The University of Liverpool, UK

Divya Chadha Manek

Divya Chadha Manek

Head of Business Development NIHR Clinical Research Network, UK

Ibrahim Nassar

Ibrahim Nassar

Professor of Organic Chemistry Ain Shams University, Egypt

George Perry

George Perry

Dean and Professor The University of Texas at San Antonio, USA

Recommended Global Pharmaceutical Sciences Webinars & Conferences

Europe & UK
Asia Pacific & Middle East



On behalf of the organizing committee, we are pleased to announce that the 3rd World Congress on Rare Diseases & Orphan Drugs September 27-28, 2023 Amsterdam, Netherlands. Rare diseases meet 2023 provides a head interdisciplinary stag for analysts to introduce the most recent research discoveries and portray developing advances, and bearings in Rare diseases and Orphan Drug. The event attempts to contribute to presenting novel research results in all aspects of Rare diseases-Orphan Drug.

The conference main aim is to unite leading academic scientists, researchers and research scholars to exchange and share their experiences and research results about all aspects of Rare diseases-Orphan Drug. It provides the first grades integrative scientists, professors, specialists, researchers, students and practitioners to represent their latest research results, taughts, developments, and applications in all areas of Rare diseases-Orphan drug. This conference will bring up with the leading academic scientists, researchers, industrial delegates, healthcare professionals and scholars in the field of interest from around the world. The main aim of this conference is to provide a scientific forum for all international prestige scholars around the world and enable the interactive exchange of state-of-the-art knowledge. This conference will mainly focus on complete evidence-based benefits proven in clinical trials and scientific experiments.Rare diseases meet 2023 comprises of well-organized scientific program coursed with interactive sessions, one to one discussion rounds, industry-academia interaction programs, industrials presentations, special regulatory sessions, and networking sessions.

Theme:  Strive for the eradication of rare diseases.

Why to attend

Rare Diseases 2023 is giving a worldwide stage to analysts that afford new insights into the concealed rare diseases. This conference will feature a global audience of scientific leaders, academia and health care professionals, and Orphan Drugs experts who are going to discuss today’s emerging treatments and diagnostics. It is designed to provide an educational forum that stimulates clinical, research, government and patient communities to create a coordinated and comprehensive approach for advancing the implementation of research, clinical care, care delivery coordination and other public health interventions critical to improved outcomes in Rare Diseases.

Who should attend?










Rare Disease Associations and Societies

Medical Colleges

Pharmaceutical Companies and Industries

Health care professionals




Training institutes

Drug manufacturing companies


Track 1 : Rare Diseases and Ultra Rare Diseases

Interest in rare diseases has expanded in recent times, as substantiated by politicians and health authorities' dockets, yet ultra-rare conditions still admit far too little attention. Although no legal bracket of an “ultra-rare" complaint has been created, the National Institute for Health and Care Excellence has informally designated this subcategory for specifics having suggestions for diseases with a frequency of lower than one in per 50 000 people. The approach, by which ultra-rare complaint exploration should be conducted, as well as the question of quality, is both critical considerations. Although lower strict criteria may be used for orphan medicinal than for medicines treating more current conditions, this shouldn't be used as a reason to deny people with rare conditions the stylish available treatment. When a case is diagnosed with a rare or ultra-rare condition, having the correct croakers and treatment plan is just as vital as having a support system.

Track 2 : Orphan Drug Therapeutics

Orphan therapeutics is pharmaceuticals used to diagnose, help, or treat life-changing or life-altering conditions or diseases that are rare. Because of the small case groups needed for clinical trials, orphan medicine development is particularly delicate. By description, rare conditions affect smaller than Americans, with some affecting only a many hundred. There are about 7000 circumstances like this. Because the pharmaceutical business has little interest in developing and promoting treatments for a bitsy number of cases, these medicines are appertained to as "orphan" medicines. The exceptionally high cost of bringing a remedial product to the request would not be covered by prognosticated deals, according to medicine makers. As a result, the prospective request for new pharmacological treatments is minimal, and the pharmaceutical assiduity would suffer a financial loss as a result. The FDA has handed several gratuities and impulses to medicinal and exploration businesses to help with drug development and treatment choices for orphan diseases.

  • Challenges in Orphan Drug Development
  • Drug Repurposing/Repositionin
  • Regulatory Considerations for Drug Repurposing
  • Future Perspectives

Track : 3 Rare Genetic Diseases/Disorders

A genetic complaint is a medical condition caused by one or further gene mutations. A chromosomal abnormality or a mutation in a single gene (monogenic) or multitudinous genes (polygenic) might beget it. Because of the high number of inheritable abnormalities, one out of every twenty-one people is affected with a" rare" inheritable complaint (generally defined as affecting lower than 1 in people). The maturity of inheritable conditions is rare in and of itself. The prevalence of rare disorders is used to define them rather than unifying pathological or clinical criteria. Rare conditions cover a wide range of pathologies and pathogenesis mechanisms since they're distinguished by their low frequency. Rare inheritable conditions serve as a springboard for uncovering new biology that has far-reaching counteraccusations for common mortal diseases. Changes in DNA are intertwined in the cause of around 80 rare diseases. Indeed if the symptoms are not constantly apparent, numerous conditions are present throughout a person's life. Rare Endocrine Genetic Diseases

  • Paediatric Rare Genetic Disorders
  • Rare Disease Genomics
  • Detection of Rare Genetic Diseases

Track 4: Challenges in Rare Diseases

With strict rules executed for unprecedented infirmities, it's to a great degree delicate to share in phenomenal sickness ask about on a subject without the backing of a clinician also constraining the clinical trials limited keeping in mind the end thing to have a trust of filling them. Generally, there's an insufficiency of benefits for exploration on exceptional conditions of disseminates included with a little request degree and nonattendance of being written work and endured specialists are some huge challenges. 452 medicines and inoculations being produced for remarkable conditions use stimulating new coherent and particular data. A strong bit of the specifics, which offer look for after those anguish from one of the rights around unknown conditions, address imaginative better ways to deal with target affliction.

Track 5 : Orphan Drugs Clinical Research

Clinical trials funding for orphan products have been shown to be a viable technique of fostering and promoting the development of novel, safe, and effective medical products for rare diseases and conditions. Orphan drug clinical development is both challenging and exciting. There is no single aspect that is truly unique to it; rather, it encompasses the majority of the challenges: design, outcomes, recruiting, ethics, cost, probability, and predictability. To solve these challenges, academic institutions, small and major pharmaceutical firms, patient representatives, and health authorities must work together to give assistance and creative ideas. The ultimate goal is to provide medications with a good benefit-risk ratio to individuals with unmet medical needs. FDA is focusing their efforts with a new funding opportunity to facilitate and move new therapies along in drug development in a safe and efficient manner by encouraging innovative clinical trial methods such as adaptive and seamless trial designs, modelling and simulations, and basket and umbrella trials to address the remaining unmet need and lack of treatments for the majority of rare diseases. These techniques are critical for effective trials and data analysis, which can help speed up drug development.

Track 6 : Global Rare Diseases and Orphan Drug Market

A rare complaint, occasionally known as an orphan complaint, is one that affects a small proportion of the world's population. Indeed if symptoms may not develop incontinently, the maturity of these rare conditions is inherited and present throughout a case's continuance. There has been an increase in the circumstance of rare conditions each across the world. An orphan medicine is a pharmaceutical product used for the opinion, forestalment, and treatment of colourful rare conditions or conditions, according to the European Organization for Rare Conditions. These conditions are distinct from other conditions in that they've a veritably low frequencies rate relative to other conditions, and so are bought by a veritably limited patient population. The global orphan medicine request was valued atUS$147.56 billion in 2019 and is prognosticated to grow at a CAGR of 10 toUS$413.36 billion by 2030.

  • Business Strategies
  • Research & Development Activities
  • Supply Chain Analysis
  • Competitive Landscape
  • Market Composition Analysis
  • Analysis and Forecasts

Track 7 : Advancing Research for rare diseases

Rare disease research is difficult due to the scarcity of patient information on the conditions. Because there are so few people affected, patient recruitment for clinical studies might be very difficult. To address these difficulties, a number of charities, patient advocacy organisations, and government agencies have developed online registries to collect patient data for researchers, doctors, and public health experts to use. It's crucial to remember that study into the aetiology, processes, and treatment approaches of rare diseases can help to advance advancements in common diseases. Rare diseases are biologically complex, and scientists are working hard to figure out what causes them and how they progress clinically. As researchers identify the molecular and genetic drivers of many diseases, we've witnessed amazing progress in the creation of medicines to treat patients with rare diseases.

Track 8 : Living with a Rare Disease

Uncommon Dis temperatures are a different miscellaneous gathering of affections with a little in like way beside of their abnormality impacting with affecting the people. 80 of uncommon ails have honored inheritable origins and others may have some natural factors, there are wide and a many which are yet to be analysed. Some uncommon ails are gained while some impacted people go about as Conditions audited. Notwithstanding anomaly, they speak to a critical medicinal and medical issue due to their event. For different uncommon distemperatures have no treatment, still in the event that it exists and if began on time as conveniently accessible to cases, there's a decent conjecture for them to be able for typical life. The issues of cases reflected and affected by uncommon distemperatures are related to the nonappearance of conclusion and accessible passing and their treatment or balancing exertion.

Track 9 : Genomics and Proteomics of Rare Disease

Despite our understanding of the inheritable mutations that uphold uncommon conditions, little is known about their cellular impacts. Because developments in genome sequencing have far surpassed the throughout in functional follow-up examinations, functional studies on rare conditions have fallen behind gene identification. Likewise, pharmaceutical and biotech enterprises have many impulses to invest in medicine exploration and development for conditions that only impact a small number of people. Rare conditions have always been delved at the cellular position on an individual base. A study published lately phenotyped a library of rare complaint-causing variations and their wild- type alleles in detail. Whole-genome sequencing can give sapience into the genetics of rare diseases; it can miss up to half of the cases that are screened. The experimenters discovered that integrating proteomics and genomics increases rare complaint individual delicacy.

  • Protein Modification
  • Protein Translation
  • Genomic Studies
  • Transcriptomics

Track 10 : Overview on Rare Diseases

An orphan drug is a pharmaceutical specialist that has been produced particularly to treat an uncommon remedial condition, the condition itself being indicated to as a fugitive sickness or uncommon infection. Fugitive specifics for the utmost part take after an indistinguishable executive advancement way from whatever other pharmaceutical item, in which testing concentrates on pharmacokinetics and pharmacodynamics, dosing, security, good and acceptability. In any case, some factual weights are dropped with an end thing to keep up enhancement force. The enhancement of fugitive specifics has been fiscally boosted through US law by means of the Orphan Drug Act of 1983.

Track 11 : Patient Concerns for Orphan Drugs

Orphan medicines are vaccines or antibodies proposed to treat, avoid or assay an orphan complaint. Cases of rare affections incorporate inheritable conditions, uncommon tumours, infectious tropic affections and degenerative infections. The meaning of uncommon affections shifts cornerwise over wards yet generally considers disease commonness, soberness and presence of indispensable remedial options.

Track 12 : Gaming and Abuse of Orphan Drugs

The 1983 Orphan Drug Act was planned to give compose associations liberal motivators to produce particulars that may not generally appear to be salutary gambles. Organizations regularly apply for a fugitive drug assignment ahead of schedule in the drug advancement handle. On the off chance that a fugitive drug is at last championed for the request, the FDA postpones the US$2.17-million customer charge that associations must pay to the FDA for new specifics. The associations also get put credits for caused clinical- trial costs, alongside seven times of request restrictiveness, amid which time signatures for relative specifics are blocked.

Track 13 : Pharmacology and Toxicology

Due to the unique characteristics of rare diseases, developing specifics for them might be delicate. The oddity of a condition makes medicine development delicate. Due to a deficit of people, well- designed clinical trials to demonstrate efficacy can be delicate to conduct, and studies substantial enough to determine major hazards are nearly insolvable to do. When no other options are available, cases may be ready to risk side goods in exchange for implicit benefits, but the benefit-to- detriment balance is delicate to quantify and may be unfavourable in some situations. Clinical pharmacology, a translational discipline, is a critical element of medicine development, including remedial development for rare conditions. Health directors have fiscal challenges when it comes to innovative medicinally, particularly orphan medicines. Individual rare diseases impact a small number of people, yet they inclusively affect a significant portion of the population. They bear our assistance.

  • Drug Repurposing
  • Safety Assessment
  • Clinical Trials
  • Patient Involvement
  • Translational Research
  • Clinical Pharmacolog
  • Orphan Drug Development

Track 14 : Revolutionary Changes

Regrettably," rare diseases" has historically been low on the public health agenda, a fact that the 350 million individuals worldwide who suffer from these conditions are well apprehensive of. This is unsurprising since, while each of these rare conditions has too little a health burden to make a simple health-economic justification, rare conditions are allowed to be just as common as other diseases. Rare complaint discovery and operation is an illustration of an area that has served from technological advancements. The integration of new drugs for rare conditions into being care systems, on the other hand, calls into question a translational drug premise that there's a direct pathway from bench to bedside. In mindfulness of the impact of patterns of clinical interventions and associated health services on cases and their families' quality of life, a range of case-acquainted issues may be most applicable to examine for incremental curatives.

Track 15 : Entrepreneurs Investment Meet

A stage meant to associate Entrepreneurs, Proposers, and Investors around the world. It's anticipated to make and encourage the most advanced and reasonable meeting place for drawing in individualities in worldwide business addresses, assessment, and prosecution of promising business studies. A fiscal specialist might discover the most noteworthy implicit enterprise openings widely, which give a great degree of profitability. For business people, this would be a perfect place to discover reasonable bookmakers and cohorts to begin as well as grow their business. In this way, it's an indefectible place to associate Entrepreneurs, Business Owners, Early Stage Companies, and Established Corporates with National or International Investors, Corporate Investors, and Implicit Business Mates.


Orphan Drugs are kind of pharmaceutical drugs that are utilized as a part of the treatment of rare genetic diseases or uncommon therapeutic conditions. The worldwide pharmaceutical medications market was esteemed at around $962.1 billion in 2012, which is the parent advertise for orphan drugs. FDA and European commission are included in giving unique kind of convention to organizations that are encountering business hindrances, for example, item rivalry and inventory network barriers. The aggregate number of infections arranged as orphan stands at around 7,000 at present, with almost 250 new maladies being annexed to this rundown every year. Orphan Drug sales expanded by $85 billion from the earlier year. That contrasts and a 2.1% decrease in general physician endorsed medicate deals, which tumbled to $645 billion. Kyprolis, a medication from onyx Pharmaceuticals for numerous myeloma, was the most encouraging new vagrant medication in 2012, with U.S deals anticipated that would reach $897 million in 2020. With the overall orphan drug market set to reach $127 billion by 2018, representing about 16% of aggregate physician recommended sedate deals it’s turning into the following field for some of pharma’s greatest leaps forward and fiercest patent wars. FDA market research analyst has estimated the global orphan drugs market to exhibit a moderate growth rate during the forecast period and is envisaged to surpass USD 156 billion by 2020 The orphan products clinical trials grants program has been accustomed to convey more than 55 items to advertising endorsement. Awards guarantee that item advancement happens in an opportune way with an extremely unobtrusive speculation. As a rule, OOPD allow subsidizing goes on for three-four years. At any one time, there are regularly 60 to 85 on-going stipend supported activities. A noteworthy part of the appropriated stores (ordinarily roughly $15 million) for a given monetary year go towards kept financing of early endorsed gifts. The fast increment in the cost of clinical trials as of late has blocked an expansion in the quantity of new OOPD awards. OOPD normally subsidizes 12-18 new concedes per financial year.


To Collaborate Scientific Professionals around the World

Conference Date September 27-28, 2023

For Sponsors & Exhibitors

Speaker Opportunity

Past Conference Report

Supported By

Journal of Infectious Diseases & Therapy Journal of Heavy Metal Toxicity and Diseases

All accepted abstracts will be published in respective Conference Series International Journals.

Abstracts will be provided with Digital Object Identifier by