5th World Congress on Advanced Clinical Trials and Clinical Research
Date: May 14-15, 2018
Place: Singapore
5th World Congress on Advanced Clinical Trials and Clinical Research, (Clinical Trials Congress 2018) hosts a wide range of Keynote presentations, Oral talks, Poster presentations, Symposia, Workshops, Exhibitions and Career development programs. It strives to bring all the Researchers, Students and Business people under one roof to share their ideas and conduct a collaborated research.
ConferenceSeries.com hosts 3000+ Global Events that includes over 1000+ International Conferences, 1000+ Symposiums and 1000+Workshops and preconference workshops on diverse Medical, Pharmaceutical, Clinical, Engineering, Science, Technology, Business and Management fields. Over 25 Million visitors flock to our websites to observe the attest developments in these fields.
Clinical Trials Congress is one of the well-established conference among Pharmaceutical Conferences organized by Conference Series Ltd.
Why to Attend???
Clinical Trials Congress 2018 Conference is a multidisciplinary program with broad participation with members from around the globe focused on learning about clinical research and its advances. The program focuses on key issues and opportunities in the clinical trial industry, including patient recruitment, site selection, data integration, existing data sources, mobile tech, project management, outsourcing, vendor management, budgeting and contracting, quality (QbD) in trial conduct, risk-based monitoring, Bioinformatics in clinical research and trials, Nano technology in clinical trials, Entrepreneurs investment meet, Post marketing surveillance and clinical auditing. This is your best opportunity to reach the largest assemblage of participants from Clinical Trials community which includes academia, clinical research entities, medical groups, related associations, societies, government agencies, pharmaceutical, biomedical device industries and many business groups.
Clinical trials congress 2018 will examine different orders required in the pre-clinical research, conduct of clinical trials; it will teach healthcare analysts about plan, operation, organizing, computation of the data, administrative angles and reporting of clinical trials. it promotes better comprehension by the overall population about the significance of clinical trials in anticipation, determination, morals related with the clinical trials and treatment of ailments. presentations, distribute information, meet with current and potential researchers, make a sprinkle with new clinical research improvements, and get name acknowledgment at this 2-days occasion. widely acclaimed speakers and the latest techniques, improvements, newest updates in clinical research are hallmark of this gathering and furthermore we attempt to empower the sprouting researchers by felicitating them with appealing prizes.
Who should attend and Who You'll Meet
Directors/Senior Directors/Executive Directors and Vice Presidents/Senior Vice Presidents/Executive Vice Presidents and Heads/Leaders/Partners of
Medical Directors, Principal Investigators, Methodologists, and other clinical research professionals along with Academicians: University Faculties like Directors, Senior Professors/Assistant Professors/ Associate Professor, Research Scholars, scientists who are related to clinical and medical research.
Clinical/Pharmaceutical and biotech industry professionals with responsibilities in:
4th International Conference on Clinical Trials
Date: September 11-13, 2017
Place: San Antonio, Texas, USA
4th International Conference on Clinical Trials, (Clinical Trials 2017) includes a wide range of Keynote presentations, Oral talks, Poster presentations, Symposia, Workshops, Exhibitions and Career development programs.
Why to Attend???
Clinical Trials 2017 Conference is a multidisciplinary program with broad participation with members from around the globe focused on learning about clinical research and its advances. This is your best opportunity to reach the largest assemblage of participants from Clinical Trials community that is from academia, clinical research entities, medical groups, related associations, societies and also from government agencies, pharmaceutical, biomedical and medical device industries.
Clinical Trials 2017 will discuss various disciplines involved in the pre-clinical research, conduct of clinical trials; it will educate health care researchers about design, operation, organizing, research computing, regulatory aspects and reporting of clinical trials. It promotes better understanding by the general public about the importance of clinical trials in prevention, diagnosis and treatment of disease. This conference conduct presentations, distribute information, meet with current and potential scientists, make a splash with new clinical research developments, and receive name recognition at this 3-days event. World renowned speakers and the most recent techniques, developments, the newest updates in Clinical Research are hallmarks of this conference.
Who Should Attend and Who You'll Meet
Directors/Senior Directors/Executive Directors and Vice Presidents/Senior Vice Presidents/Executive Vice Presidents and Heads/Leaders/Partners of
Medical Directors, Principal Investigators, Methodologists, and other clinical research professionals along with Academicians: University Faculties like Directors, Senior Professors/Assistant Professors/ Associate Professor, Research Scholars, scientists who are related to clinical and medical research.
Clinical/Pharmaceutical and biotech industry professionals with responsibilities in:
2nd International Conference on Clinical Trials and Therapeutic Drug Monitoring
Date: August 22-24, 2016
Place: Philadelphia, Pennsylvania, USA
2nd International Conference on Clinical Trials and Therapeutic Drug Monitoring is a multidisciplinary approach. Drug concentration measurements are requested to assist the management of a patient's current medication regimen or to screen for a medicine. The Drug Monitoring studies are performed for monitoring drugs with narrow therapeutic ranges, drugs with marked pharmacokinetic variability, medications for which target concentrations are difficult to monitor, and drugs known to cause therapeutic and adverse effects. The process of TDM is predicated on the assumption that there is a definable relationship between dose and plasma or blood drug concentration, and between concentration and therapeutic effects. Accurate and clinically meaningful drug concentrations are attainable only by complete collaboration by a TDM team, typically comprised of scientists, clinicians, nurses, and pharmacists. OMICS International organizes a conference series of 1000+ Global Events inclusive of 300+ Conferences, 500+ Upcoming and Previous Symposiums and Workshops in USA, Europe & Asia with support from 1000 more scientific societies and publishes 700+ Open access journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.
Why to Attend??
Drug Monitoring 2016 gives you access to leading-edge pharmaceutical information and valuable new professional contact from all over the world. Its large international participation provides excellent opportunities for global sharing of technology, expertise, products, and best practices. There are exhibitions which run in parallel with the conference and offer you the chance to get up-to-date information from companies active in your area of interests. We are grateful to our sponsors and exhibitors for their interest and support for the conference.
Target Audience:
International Conference on Clinical Trials
Date: July 27-29, 2015
Place: Orlando-FL, USA
The International Conference on Clinical Trials, with target audience as Principle Investigators, Methodologists and CRO/Industry professionals, the conference will focus on prevailing approaches in various Clinical Trials and how to increase its efficiency during different phases of trials to develop low cost therapeutic approach with higher efficacy. OMICS International Organizes 300+ conferences, 500+workshops and 200+symposiums on Clinical, Medicine, Pharma and Science & Technology every year across USA, Europe, Asia, Middle East, Australia and UK with support from 1000 more scientific societies and Publishes 500 open access journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.
Clinical Trials Management System has made enormous progress in past few years, and according to Transparency Market Research the estimated net worth is approximately US$844 million in 2013, while growing at a compound annual growth rate of 14% during the forecast period, the worldwide Clinical Trials Management System market is expected to acquire market value worth US$1,848.5 million by 2019. United States is the major center in the field of Clinical Trials with Florida being one of its major contributing states. Florida is considered to be a hot spot for various investigation sites of different Pharmaceutical Industries and Medical devices. Florida, Orlando, Miami and Tampa are major cites which are focused for Clinical Trials and Research.
