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Rare Diseases Meet 2020

7th Global Congress on Rare Diseases & Orphan Drug 2020

Dubai, United Arab Emirates
18 - 19 June 2020
The conference ended on 19 June 2020

Important Dates

Early Bird Deadline
28th March 2020
Abstract Submission Deadline
13th April 2020

About Rare Diseases Meet 2020

Conferences Series invites all the Nobel laureates, speakers, delegates, microbiologist from all over the world to attend “7th Global Congress on Rare Diseases & Orphan Drug” during June 18-19, 2020 in Dubai, UAE.

Topics

Orphan diseases and public health, Rare cardiac diseases, Neglected rare tropical diseases, Rare oncology diseases, Rare aging diseases, Rare oral diseases, Rare genetic diseases, Rare neurological disorders, Hematological disorders, Gene therapy for rare diseases, Rare obesity and metabolic disorders, Allergic and immunologic disorders, Clinical trials and treatment, Orphan drugs- development trends and strategies, Pediatric rare diseases, Future hereditary of rare diseases and orphan drugs, Drug approvals for rare diseases

Call for Papers

Rare Diseases Meet 2020  folds reputed scientists, researchers and faculty from universities and research institutions, Dermatologists, Pharmacists, Bacteriologists, Virologists, Ophthalmologist, Microbiologists, Orphan Drugs Companies, Anesthesiologists, CEO’s, Presidents of societies, business delegates, Parasitologists, young researchers and talented student populations under a solitary gable catalyzing information exchange for the advancement of research in the field of Orphan diseases and public health, Allergic and Immunologic Disorders, Pediatric rare diseases, Infectious Diseases, Clinical Trials and Treatment, Rare Neurological Disorders, Neglected Rare Tropical Diseases, Gene Therapy for Rare Diseases, Hematological Disorders,  Rare Obesity and Metabolic Disorders, Rare Oncology Diseases, Rare Oral Diseases, Rare Aging Diseases, Rare Genetic Diseases, Rare Cardiac Diseases, Orphan Drugs- Development Trends and Strategies, Drug Approvals for Rare Diseases, Future Hereditary of Rare Diseases and Orphan Drugs

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