Theme: Exploring the Advancements in Cell and Gene Therapy
Cell gene Therapy 2019
- About Conference
- Session and Tracks
- Market Analysis
- Past conference Report
- Visa and Trip advisor
- Submission Deadlines
- Abstract Submission Criteria and Eligibility
Cell gene therapy 2019 takes intense pleasure and honour in welcoming you all for “International Conference on Cell and Gene Therapy” during November 26-27, 2019 at Lisbon, Portugal. Prominent keynote speakers, plenary speeches, young research forum, poster presentations, technical workshops and career guidance sessions are involved in the conference.
The conference focusses with an exciting Theme on “Exploring the advancements in Cell and Gene Therapy”.This scientific session offers a great platform with its well defined scientific sessions to the audience to share and express their innovative ideas on topics like Gene Therapy, Cell Therapy, Immunotherapy, Biomarkers, Stem cell in Gene therapy, Genomics, Tissue Science and Regenerative medicine, Viral Gene therapy, Epigenetics, Proteomics, Genome Editing, Nanotherapy, Advanced Gene Therapeutics and much more .
Significance of Cell and Gene Therapy Conference:
Cell and gene Therapy Conferences is enhance propels methods and presentation of recent improvement to the revelation of advances in Cell and genetic field and Gene therapy is useful in inadequate qualities responsible for treatment of diseases using advancement and Cellular Therapies which is efficacious to deliver Regenerative Cells and aides in quality in Cellular development of Tissues.
Cell gene Therapy 2019 provides a Universal Platform to fulfil and provide innovative research on Novel and future methodologies in assuaging infections and provides combination of Researchers, Geneticist, Biologists ,Business Delegates of Specific companies and Scientists to fulfil and provide concerning recent strategies and Advances on the various circle. Cell gene Therapy 2019 Conferences main concentration is uniting Scientists, Physicians, International mix of driving Universities, Cell therapy institutions to share their examination valuable for restoring of Genet, diseases and facilitate in approaches for new strategies through our Conference.
Cell gene Therapy 2019 can address key problems regarding disease viewpoints in Genetic and Hereditary malady and encourages in achieving learning receptive to society.
Target Audience:
- Cell Therapy Scientists, Researchers and Students
- Biotechnologists
- Gene Therapy Researchers, Scientists and Students
- Cell and Gene Therapy Faculties
- Stem Cell Lecturers
- Immunologists
- Genetic Engineering Researchers
- Immunologists
- Health-care professionals
- Business Entrepreneurs
Track 1: Gene Therapy
Gene therapy essentially involves the introduction or alteration of genetic material among the cell or organism with associate intention of curing of the sickness. The individual cell therapy and gene therapy uses overlapping fields of medical analysis with the goals of repairing the direct Genetic diseases in polymer or cellular population respectively, the invention of DNA technology within the 1970’s provided tools with efficiency develop gene theraphy. Scientists use these techniques to promptly manipulate infective agent genomes, isolate genes and establish mutations concerned in human sickness, characterize and regulate sequence expressions, and engineer numerous infective agent and non-viral vectors. Numerous long-term treatments for anemia, hemophilia, mucoviscidosis, genetic defect, Gauscher’s sickness, lysosomal storage diseases, vas diseases, polygenic disease and diseases of bones and joints are resolved through successful gene therapy.
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Europe: European Society of Gene and Cell Therapy(ESGCT), Thierry Latran Foundation, UK Stem Cell Bank, Cambridge Stem Cell Initiative, Stem Cell Network North Rhine-Westphalia, European Federation of Immunological Societies, EuroStemCell (European Consortium for Stem Cell Research), European Biophysics Programs - Biophysical Society
United States: North Carolina Integrative Medicine Society, Alternative and Integrative Medical Society, American Association of Integrative Medicine, Society for Integrative and Comparative Biology, Canadian Integrative Cancer Therapies Association.
Asia: Stem Cell Society Singapore, All India Institute of Medical Sciences (AIIMS), National Centre for Biological Sciences, Tiantan Puhua Stem Cell Center China, Indian Pancreas Club, Taiwan Society for Stem Cell Research, Alzheimer’s Cure Foundation
Track 2: Cell Therapy
Cell therapy or cytotherapy is the transfer of cells into a patient with a goal of curing the illness. From starting blood transfusions were thought of to be the primary form of cell therapy to be experienced as routine. Later, Bone marrow transplantation has conjointly become a well established idea that involves treatment of the many reasonably blood disorders together with anemia, leukemia, lymphyoma and rare immunological disorder diseases. Various medical practitioners perform cell therapy within the kind of many completely different names together with transplantation therapy, organ therapy, and recent cell therapy. It's been claimed by the proponents of cell medical care that it's been used with success to repair medulla spinalis injuries, strengthen weaken system, treats reactive diseases like AIDS, facilitate patients with medical specialty disorders like Alzheimer’s illness, parkinson’s illness and brain disorder.
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Track 3: Immunotherapy
Due to quick pushing field in study of neoplasm, there has been age of some of latest procedures for treating development known as Immunotherapies. This therapy may be a variety of treatment that extends the character of safe response against tumors either by enabling the activities of specific sections of safe structure or by checking signals sent by sickness cells that covers safe responses. Some of forms of therapy are known as life treatment or biotherapy. Late movements in development immunotherapies have given new adjuvant systems. The treatment in-situ commencement of platelets with stop inhibitors for post-careful development therapy ,centers in oncology,safe stop blockade and connected endocrinopathies use the tumors associated with macrophages.’
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Track 4: Biomarkers
Biomarkers have rapid evolvement in the advance of personalized medicine and individual health Biomarkers refers to a broad subcategory of medical signs which include objective indications of medical state that are determined from outside the patient – which might be measured accurately and reproducibly. Medical signs change distinction to medical symptoms, that are restricted to those indications of health or sickness perceived by patients themselves.
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Track 5: Stem Cell in Gene Therapy
Stem cell treatment is a process where the stem cells are used to make disease free of life through treatment of diseases. They have the potential to treat various life threatening diseases. The unique feature of these cells to divide into multiple stem cells and differentiate into specialized cells make them apt for the treatment of many diseases. The present researches suggest that stem cells can be used for treating the genetic disorders as well. Apart from treating diseases like brain injuries, Osteoarthritis, diabetes, learning disabilities, various types of blood cancer,Sickle cell anemia, Parkinson’s, Haemophilia, and Thalassemia, etc. The cell defect due to mutation result in a wide of variety of genetic disorders. The transplantation of stem cells where the normal stem cell replaces the defected cells can be used for treatment of genetic disorders and diseases.
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Track 6: Genomics
Genomics is a part within genetic science that involves the sequencing in analysis of an organism’s ordering. It additionally involves the study of intragenomic processes like biological process, heterosis and pleiotropy still because the interactions between loci and alleles inside the genome. The fields of genetics and molecular biology are primarily involved with the study of the role and performance of single genes, a serious topic in today’s biomedical research. It does not involve single gene research unless the purpose is to understand a single gene’s effects in context of the entire genome.
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Track 7: Tissue Science and Regenerative Medicine
Tissue science is essentially study and understanding the organization of tissue during a complexed human system and its structure and functions of it. As we tend to all understand that every tissues tends to make the organ.so it’s all necessary to know concerning the tissues
Regenerative Medicine is that the a part of translational analysis in tissue engineering and biology. This field contains the hope of engineering broken tissues and organs. Regenerative medicine has the risk of growing tissues and organs within the laboratory and implanting them so as to administer the capability to the body to heal by itself. If a regenerated organ's cells are basically derived from the patient's own tissue or cells, this could facilitate to discover the matter of the shortage of organs obtainable for donation, and also the downside of surgical procedure rejection.
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Track 8: Viral Gene Therapy
Applications of infectious agent vectors have found an encouraging new starting in sequence medical aid in recent years. Important enhancements in vector engineering, delivery, and safety have placed infectious agent vector-based medical aid at the forefront of recent medication. Infectious agent vectors are used for the treatment of various diseases like metabolic, vas, muscular, haematological, ophthalmologic, and infectious diseases and differing types of cancer. Recent development within the space of therapy has provided each preventive and therapeutic approaches. moreover, sequence silencing generating a reversible impact has become a noteworthy various, and is well-suited for delivery by infectious agent vectors. Variety of presymptomatic studies have incontestible therapeutic and prophylactic efficaciousness in animal models and moreover in clinical trials. Many infectious agent vector-based medication have additionally been globally approved.
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Track 9: Epigenetics
Epigenetics provides a software system that packages deoxyribonucleic acid, while not dynamical the first base sequence, to ascertain inherited patterns of organic phenomenon. In cancer, several aspects of the epigenome, controlled by deoxyribonucleic acid methylation, chromatin, and nucleosome positioning, square measure altered united suggests that by that tumour cells maintain abnormal states of self-renewal at the expense of traditional maturation. Epigenetic and genetic abnormalities therefore collaborate in cancer initiation and progression, as exemplified by frequent mutations in genes encryption proteins that management the epigenome. There is a growing stress on exploitation epigenetic therapies to reprogram growth cells toward a standard state. Several agents targeting epigenetic regulation square measure beneath development and coming into clinical trials.
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Track 10: Proteomics
Proteomics can be defined as broad scale examination of proteomes. A protein could be a course of arrangement of proteins created during a living being, structure, or regular setting. Which could be tend to apply. For example, the protein of a creature composes (for example, Homo sapiens) or an organ (for example, the liver). The protein is not relentless; it fluctuates from cell to cell and changes when your time. To some extent, the protein reflects the key transcriptome. Regardless, macromolecule activity (regularly reviewed by the reaction rate of the systems during which the macromolecule is incorporated) is equally modified by varied parts despite the verbalisation level of the suitable quality.
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Track 11: Genome Editing
Genome editing is that the deliberate alteration of a specific desoxyribonucleic acid sequence in a very living cell. A strand of desoxyribonucleic acid is cut at a particular purpose and naturally existing cellular repair mechanisms, then fix the broken desoxyribonucleic acid strands. The approach they're repaired will have effect on gene performand new desoxyribonucleic acid sequences is delivered once the desoxyribonucleic acid is cut and act as templates for generating an altered sequence. Genome editing techniques is applied to delete sections of desoxyribonucleic acid or alter however a gene functions: for instance, by dynamic a variant that will create to malady to at least one that functions unremarkably.
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Track 12: Nanotherapy
Targeted nanotherapeutics could be a novel strategy for treating a range of diseases associated and is a rising technology that provides benefits over current treatment ways. The nanoscale size, combined with the flexibility to surface functionalize the delivery vehicle to alter targeting and incorporate a therapeutic payload, give a brand newand innovative therapeutic platform to treat surgical diseases that has nevertheless to be absolutely accomplished within the surgical arena.
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Track 13: Advanced Gene Therapeutics
Therapeutics is that the branch of science handling the appliance of remedies of diseases. The medication of gene therapeutics is tend to develop a remedy for a sickness through the genetic material.
Advanced gene therapeutics may be a medication which use the medicine to treat a sickness by developing dose forms to optimize drug action, underpin new formulations that concentrate on molecules spatially inside the body, enhance the bioequivalence of poorly soluble medicine and biologics, and improve patient expertise and compliance
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Track 14: Clinical Trials on Cell & Gene Therapy
Clinical Trials of Cell and gene therapy product usually variable from the clinical trials design for alternative varieties of pharmaceutical product. This variations in trial design that are necessitated by the distinctive options of those product. The clinical trials additionally replicate previous clinical expertise and proof of drugs. Early experiences with Cell and gene therapy product indicate that some CGT product might cause substantial risks to subjects because of impact at cellular and genetic level. The planning of early-phase clinical trials of Cell and gene therapy product usually involves the subsequent thought of clinical questions of safety, diagnosing problems, and chemistry, producing and controls (CMC) problems that can be encountered
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Market Analysis:
Cell gene therapy 2019 cordially invites you all to join us on International Conference on Cell and Gene Therapy scheduled during November 26-27, 2019 at Lisbon, Portugal. The conference was taking place under the theme on “Exploring the advancements in Cell and Gene Therapy”.
For more details: https://genetherapy.geneticconferences.com/
Scope: Scope of the meeting is to assemble each one of the Doctors, Researchers, Business Delegates and Scientists to approach and convey each one of the participants regarding the premier current logical headways. It is the variable circle or associated logical controls .This Cell and succession treatment Conference is that the top knowledge understanding individual and structure conduct and basic leadership with relevance science examination and bioscience, biotechnology, pharmaceuticals, medicals and other areas.
Importance: Gathering on Cell therapeutic care can be a bottomless praised meeting that essentially manages the foremost current investigation and enhancements within the circle of Cell and natural science. This Conference will provides a excellent stage to any or all the International mix of driving investigation understudies, and Scientists accomplished distinction in their field of study, examination academicians from the universities and investigation foundations, mechanical examination specialists and business connects along side pH scaled. Understudies to come back and educate each one of the participants with reference to the most recent logical headways on the few circles.
Why Lisbon???
Lisbon is the stunning capital city of Portugal, and is one of the most charismatic and vibrant cities of Europe. It is a city that effortlessly blends traditional heritage, with striking modernism and progressive thinking.As a holiday destination, Lisbon offers a rich and varied history, a buzzing nightlife and is blessed with a glorious year-round climate. Lisbon is a bustling and exciting city, that boasts a wide choice of activities and fascinating tourist attractions. The city has a welcoming and liberal atmosphere, while still embracing its deep-rooted heritage and extensive history. Lisbon will appeal to a diverse selection of ages and tourists; it can form a cultural trip, a nightlife extravaganza, a family holiday, a relaxed city-break or even as a base for a beach holiday. Lisbon has hot dry summers, pleasant springs and autumns, and mild, but possibly wet winters. The best time of year to visit Lisbon is in the late spring (May-June) when the days are bright and sunny, but the temperatures are not so high. The peak season is between June and August, and if you visit at this time of year, you should expect the city to feel crowded. The weather is suitable for spending time on the beach from May until the end of September.
Global Cell Therapy Market:
Cell medicinal guide item, that region unit got from dedifferentiated cells, tissues, and organs develop in labs, region unit infused into patients. The developing assortment of clinical preliminaries, government and individual finance, and increasing scope of associations between corporations territory unit driving the extension of the globe cell restorative guide advertise. "Cell and Sequence restorative guide item that region unit offered within the market depends on autologous and allogeneic cells. The raise of cell treatment is increasing."
Quality restorative guide includes connection of an engineered or a modified succession misuse modified irresistible operator vectors that encourage convey the grouping at implicit site of activity or even execute the cell which can cause the disease. This treatment is for the foremost part a one-time treatment or wants simply few measurements of prescription to fully fix the disease.
The examiners estimate the globe cell therapeutic guide market to develop at a CAGR of 9.5% during the year 2019-2026. The report covers this scenario and on these lines the event prospects of the globe cell therapeutic guide business center for 2019-2026. The report introduces a close-by image of the market by strategies for study, blend, and summation of information from varied sources.
List of university in Lisbon:
- Nova University of Lisbon
- Catholic University of Portugal
- ISCTE – University Institute of Lisbon
- Universities Lusíada of Lisbon
List of university in Portugal:
- University of the Azores
- University of Algarve
- University of Aveiro
- University of Beira Interior
- University of Évora
- University of Coimbra
- Atlantic University
- Lusófona University
- University of Oporto
- University of Tras-os-Montes and Alto Douro
- University of Madeira
- Open University
Top Universities around the Globe
- University of Washington/Hutchinson Cancer Center
- Oregon Stem Cell Centre
- University of California Davis
- King's College London
- Cambridge university
- Oxford University
- Middlesex University
- University of Glasgow
- University of Manchester
- University of Edinburg
- Charles university
- University of Uppsala
- University of Bristol
- University of Italy
- Imperial college of London
- Bakers laboratory centre
- Max plank Davis centre
- University of duke
- Stanford University
Statistical Analysis of universities
List of Companies Associated with Cell and Gene Therapy Research
- Bellicum Pharmaceuticals
- BIOCELLULAR THERAPIES
- Bio-Tissue
- BioTissue Technologies
- Bluebird Bio
- Caladrius
- CellBioMed
- Cell Medica
- CellSeed
- Celyad
- CRC for Cell Therapy Manufacturing
- Cynata Therapeutics
- DiscGenics
- Cytori Therapeutics
- Dendreon
- Fibrocell Science
- Fortress Biotech
- GlaxoSmithKline
- Histogen
- Holostem Terapie Avanzate
- Immunocellular Therapeutics
- Intercytex
- Janssen Pharma
- Juventas Therapeutics
- Kite Pharma
- LifeNet Health
- Lonza
- MEDIPOST
- Nanofiber Solutions
- Neuralstem
- Northwest Biotherapeutics
- Ocata Therapeutics
- Orbsen Therapeutics
- Pharmicell
- Prima BioMed
- Regenerexx
- Regenerys
- Regrow
- ReproCELL
- RenovaCare
- Vericel
- RESSTORE
- ReNeuron
- RepliCel
- Regience
- Regeneus
- Q Therapeutics
- Pluristem Therapeutics
- Pfizer
- Opexa Therapeutics
- NovaRx
- Newlink Genetics
- Nanotope
- Mesoblast
- MaxCyte
- Living Cell Technologies
- Kiadis Pharma
- Kensey Nash
- Juno Therapeutics
- ISTO Technologies
- Integra Life Sciences
- Humacyte
- Histogenics
- Healthpoint
- Gamida Cell
- Forticell Bioscience
- Fate Therapeutics
- DiscGenics
- Cynata Therapeutics
- Cytori Therapeutics
- CryoLife
- CESCA THERAPEUTICS
- CellPraxis
- Celgene
- Capricor Therapeutics
- Bone Therapeutics
- BrainStorm Cell Therapeutics
- BIOTIME
- Biogen Idec
- BioCardia
- AxoGen
- Athersys
- Antibe Therapeutics
- Amorcyte
- Antibe Therapeutics
Top Major Societies Associated with Cell and Gene Therapy
- International Society for Cancer Gene Therapy (ISCGT)
- Australasian Gene Therapy Society (AGTS)
- British Society of Gene Therapy (BSGT)
- Swedish Society for Gene and Cell Therapy (SSGCT)
- Austrian Network for Gene Therapy
- German Gene Therapy Society (DGGT)
- Spanish Society of Gene and Cell Therapy (SETGyC)
- Israeli Society of Gene & Cell Therapy (ISGCT)
- Finnish Gene Therapy Society (FGTS)
- Netherlands Society of Gene and Cell Therapy (NVGCT)
- Irish Society for Gene & Cell Therapy (ISGCT)
- American Society of Gene and Cell Therapy (ASGCT)
- Japan Society of Gene Therapy (JSGT)
- British Society and Gene and Cell Therapy
- Korean Society of Gene and Cell Therapy (KSGCT)
- Société Francophone de ThérapieCellulaire et Génique (SFTCG)
- European Society of Gene and Cell Therapy (ESGCT)
- Turkish Society of Gene & Cell Therapy (TSGCT)
Pie Chart between Companies and Societies associated
Market Value on Cell and Gene Therapy:
Gene medical care may be a attractive area for drug development as a result of with the proper target and approach; it will address the premise reason for a severe malady. Evidently disorders where acknowledged genetic mutations as a result of deficient or non-functional molecule production, sequence medical care can fix the underlying defect and provide a path to produce the sensible molecule.
The worldwide sequence medical care market was valued at $584 million in 2016, and is determinable to reach$4,402 million by 2023, registering a CAGR of 33.3% from 2017 to 2023. the increase in funding for R&D activities referring to sequence medical care and increase in awareness regarding sequence medical aid unit the foremost vitalfactors that drive the market growth.
Cell gene therapy 2019 Report
Thanks to all of our marvellous speakers and conference attendees for making the conference a grand success.
The International Conference on Cell and Gene Therapy was hosted by the Conference Series on November 26-27, 2019 at Lisbon, Portugal with the theme “Exploring the Advancements in cell and gene therapy ". Benevolent response and active participation was received from the scientists, engineers, researchers, students and leaders from the fields of genomics and genetic Engineering, who created this event victorious.
Our organizing committee would like to give a special thanks to our moderator Gheorghita Menghiu from West University of Timisoara who put the esteemed effort for smooth running of conference.
The meeting was distributed through numerous sessions, during which the discussions were persevered the subsequent major scientific tracks:
· Nanotherapy
· Advanced Gene Therapeutics
· Clinical Trials on Cell & Gene Therapy
· Gene Therapy
· Cell Therapy
· Immunotherapy
· Biomarkers
· Stem Cell in Gene Therapy
· Genomics
· Tissue Science and Regenerative Medicine
· Viral Gene Therapy
· Epigenetics
· Proteomics
· Genome Editing
The conference was initiated with a series of lectures delivered by both Honourable Guests and members of the Keynote forum .The list included:
Clelia Rejane Antonio Bertoncini, University of São Paulo, Brazil
Alex M Mawla, University of California, USA
Iftikhar Qayum, Rehman Medical Institute, Pakistan
Joanne D. Caguiat, Philippine Rice Research Institute, Philippines
Leen Abu Safieh, King Fahad Medical City Research Cente,Saudi Arabia
Isaac Adeyemi Adeleye, University of Lagos, Nigeria
Conference Series Ltd offers its heartfelt appreciation to Organizing Committee Members; adepts of field, various outside experts, company representatives and other eminent personalities who supported the conference by facilitating the discussion forums .Conference Series also took privilege to felicitate the Organizing Committee Members who supported this event.
With the grand success of Cell gene therapy 2019, Conference Series Ltd is proud to announce the "2nd International Conference on Cell and gene therapy” scheduled during June 22-23, 2020 at Paris, France.
For more details visit: https://genetherapy.geneticconferences.com/
Planning a Trip to Lisbon?? Attend our Meeting!!!
Issue with VISA!!
Cell gene Therapy 2019 Committee will be glad to help you in all regards to plan your trip to Lisbon, Portugal. Get the official invitation letter from us to attend this event and ahead with a closer step for approval of your VISA
Mail to: smithcaro44@gmail.com
City Attractions of Lisbon:
- Castelo de são jorge.
- Mosteiro dos jerónimos.
- Museu calouste gulbenkian.
- Museu nacional de arte antiga.
- Torre de belém.
- Padrão dos descobrimentos.
- Serra de sintra.
- Arco da rua augusta.
- Igreja do carmo.
- Basílica da estrela. and many more...
NOTE: The invitation letter will be provided after the attendee confirms his/her participation by reserving their delegate/ speaker slot for the conference.
Submission Deadlines
Early Bird Abstract Submission: July 15, 2019
Second Line Abstract Submission: August 25, 2019
Final Submission Deadline: October 20, 2019
Registration Deadlines
Early Bird: August 10, 2019
Second Round: Septmebr 20, 2019
Final Registration: November 26, 2019
Abstract Submission Criteria & Eligibility
PRESENTATION REQUIREMENTS:
- Presenting authors are responsible for registration, travel, and hotel costs. Note: Those with accepted abstracts will receive an acceptance mail allowing them to register for the conference.
- Abstracts will be compiled and conference books are made available to participants at the conference.
- Any presenter who is unable to attend should arrange for another qualified individual to present the paper/poster in question. If such a change is necessary, please notify our conference team
SUBMISSION OPTIONS:
- Oral paper presentations will have 30-minute time slots and be clustered by theme into sessions. The keynote session will have for 45-minute time slot, workshop/ special session will have 60-minute time slot and symposium will have 60-minute time slot followed by 5-minute Q&A session.
- Graduate & Masters students are eligible to submit their abstracts under poster and e-poster presentation category.
- Ph.D. students are eligible to submit their abstract under special YRF (young researcher’s forum), poster and e-poster presentation category.
NOTE: YRF category includes short oral presentation especially for Ph. D. students
- Extended abstract: Submissions should utilize the Abstract Template. Papers submitted in this category may represent original empirical research, theoretical development, reviews, or critiques.
To share your views and research, please click here to register for the Conference.
To Collaborate Scientific Professionals around the World
Conference Date | November 26-27, 2019 | ||
Sponsors & Exhibitors |
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Speaker Opportunity Closed | Day 1 | ||
Poster Opportunity Closed | Click Here to View |
Useful Links
Special Issues
All accepted abstracts will be published in respective Our International Journals.
- Journal of Molecular & Genetic Medicine
- Journal of Medical Microbiology & Diagnosis
- Journal Of Bioprocessing & Biotechniques
Abstracts will be provided with Digital Object Identifier by