Online / Physical Event

2nd World congress on


Theme: Navigating the Future of Advanced Clinical Research and Clinical Trials

Event Date & Time

Event Location

Texas , USA

Program Abstract Registration Awards

18 years of lifescience communication

Performers / Professionals From Around The Globe

Tracks & Key Topics


Academic Key Topics


Business Key Topics




EuroSciCon welcomes you to attend the 2nd World Congress on Advanced Clinical Research on February 25-26, 2022., at Texas , USA,and this we focus on the theme “Navigating the Future of Advanced Clinical Research and Clinical Trials “. Clinical Research 2022 includes prompt Keynote presentations, Oral talks (Speaker forum and Young research forum), and Poster presentations, Workshops, Symposium and Exhibitions.

Clinical Research 2022 is a global overview which will provide an international platform for the discussion of Clinical research & trials. This event gathers all the eminent persons, professors, scientists, doctors, medical practitioners, health workers, professionals, students, and industrialists all over the world to exchange their ideas, researches and their experiences. 

 Why to attend our conference

World Forum on Advanced Clinical Research and Clinical Trials Conference is a multidisciplinary program with wide support with individuals from around the world concentrated on finding out about clinical research and its advances. This is your best chance to achieve the biggest array of members from Clinical Trials, Clinical Research and Epidemiology people group that is from the scholarly community, clinical research elements, restorative gatherings, related affiliations, social orders and furthermore from government organizations, pharmaceutical, biomedical and medicinal gadget enterprises.

Clinical Research 2022 will examine different orders engaged with the pre-clinical research, lead of clinical preliminaries; it will teach medicinal services scientists about outline, activity, sorting out, explore processing, administrative perspectives and detailing of clinical preliminaries. It advances better comprehension by the overall population about the significance of clinical preliminaries in counteractive action, determination and treatment of malady. Lead introductions, circulate data, meet with ebb and flow and potential researchers, make a sprinkle with new clinical research advancements, and get name acknowledgment at this 2-days occasion. Widely acclaimed speakers and the latest strategies, improvements, the most up to date refreshes in Clinical Research and empowering world toward directing Clinical Research and Clinical Trials are signs of this gathering.

Target Audience

Target audience for Clinical Research 2022 Includes

  • CROs and CMOs
  • Directors of Clinical Research Sites
  • Pharma/Biotech and Medical Device industries
  • Hospitals
  • Clinical Associations
  • Clinical research institutes
  • Societies
  • Medical Directors
  • Principal Investigators
  • Methodologists
  • Clinical research professionals
  • Academicians
  • University Faculties
  • Research Scholars
  • Scientists
  • Students

Clinical/Pharmaceutical and biotech industry professionals with responsibilities in:

  • Clinical Research & Development 
  • Clinical Bioinformatics
  • Clinical Nanotechnology
  • Clinical Design/ Protocol Design/ Clinical Strategy
  • Global Clinical Operations/ Clinical Outsourcing 
  • Biostatistics/Data management
  • Patient Recruitment/Enrollment 
  • Clinical Trial Management/Clinical Trial Supplies
  • Regulatory Affairs

Opportunities for Conference Attendees:

For Researchers & Faculty:

  • Speaker Presentations
  • Poster Display
  • Symposium hosting
  • Workshop organizing

For Universities, Associations & Societies:

  • Association Partnering
  • Collaboration proposals
  • Academic Partnering
  • Group Participation

For Students & Research Scholars:

  • Poster Competition (Winner will get Best Poster Award)
  • Young Researcher Forum (YRF Award to the best presenter)
  • Student Attendee
  • Group Registrations

For Business Delegates:

  • Speaker Presentations
  • Symposium hosting
  • Book Launch event
  • Networking opportunities
  • Audience participation

For Companies:

  • Exhibitor and Vendor Booths
  • Sponsorships opportunities
  • Product launch
  • Workshop organizing
  • Scientific Partnering  
  • Marketing and Networking with clients



Track 1: Clinical Research

Clinical research is a part of medicinal services science that decides the wellbeing and viability (adequacy) of meds, gadgets, analytic items and treatment regimens proposed for human utilize. These might be utilized for anticipation, treatment, analysis or for diminishing side effects of an infection. Clinical research is unique in relation to clinical practice. In clinical practice set up medications are utilized, while in clinical research proof is gathered to set up a treatment. Once the promising candidate or the molecule is identified in the lab, it is subjected to pre-clinical studies, human cell studies or animal studies where different aspects of the test article including its safety toxicity and efficacy, are studied, moreover this study will help us to take the drug or molecule to large scale population which is collectively known as clinical trials which is carried out in different phases and set of population.

Track 2: Innovations in Clinical Trials & Research

Clinical survey design includes the measure of study volunteers, their division in perspective of contrasting factors, and their treatment all through the clinical preliminary handle. Analyze design is a key piece of clinical preliminaries, and the treatment of all patients particularly impacts the quantifiable authenticity of data. Consider hoard errand has similarly been broadly improved starting late. Experts have found numerous favorable circumstances to randomized undertaking versus observational errand, in light of characteristics like sex, age, race, etc., The randomized method has been found to yield more tried and true results than observational audit assignments.

Starting late, the use of Adaptive arrangement strategies in clinical research has ended up being logically outstanding a direct result of its flexibility and adequacy. Adaptable designs offer the likelihood to diminish look at range and patient presentation while expanding the probability of a productive outcome. Another advancement in clinical preliminaries is the Bucket plan. Bowl preliminaries are planned to utilize one particular drug and test that medicine against different unmistakable ailments. The advantage of this methodology is that patients with different diseases can be "pooled" together under one greater preliminary as opposed to bundles of more diminutive preliminaries, thusly saving time and resource in an equivalent methodology, and there are more headways in clinical preliminaries.

Track 3: Pharmacovigilance & Drug Safety

Pharmacovigilance (PV or PhV), also known as drug safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. The main purpose of Pharmacovigilance and Drug Safety is to disseminate the information regarding safety, efficacy, side effects, adverse effects, and toxicity of the new interventional drug. Pharmacovigilance heavily focuses on adverse drug reactions, or ADRs, which are defined as any response to a drug which is noxious and unintended, including lack of efficacy the condition that this definition only applies with the doses normally used for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological disorder function was excluded with the latest amendment of the applicable legislation. Safety monitoring of medicines is a continuous process, it is performed during clinical trials when medicines are developed, once medicines are launched and throughout the entire period where a medicine is available for patients to use. Medication errors such as overdose, and misuse and abuse of a drug as well as drug exposure during pregnancy and breastfeeding, are also of interest, even without an adverse event, because they may result in an adverse drug reaction.

Track 4: Clinical Trials

Examinations or observations done to find out the effectiveness or efficacy of clinical research is known as clinical trials. Clinical trials have designed in 3 stages such as pre-clinical studies, clinical trials in 4 phases and post clinical studies where it involves different population in countries and regions. Clinical trial phase start with drug design and drug discovery then proceed on to animal testing, which is known as pre-clinical studies.  If the pre-clinical studies give expected results then researches begin the clinical phase of development by testing for safety in a few human subjects this set of studies will be carried out in different set of population which varies in number, region, race, gender and age. Further they will expand research to test in many study participants to determine if the treatment is effective.

Clinical trials are of 3 types

  • Clinical Trials of drugs
  • Clinical Trials of devices
  • Clinical Trials of procedures

This session provides the exclusive opportunity to discuss the outcomes or efficacy of the generic drugs which is undergoing clinical trials.

Track 5: Clinical and Experimental Dermatology

Clinical Dermatology is the specialty of medicine that encompasses the complete range of diseases and conditions of the skin, hair and nails. Clinical Research carried out in order to find new generic medicines and formulations for the diseases associated with skin, hair, and nails is termed as experimental dermatology. These set of experiments must get the get FDA approval since its plays a major part in Human life. This session deals with the clinical and experimental clinical research carried out to get the better, smarter and sustainable beauty & health products.

Track 6: Clinical Biotechnology & Clinical Bioinformatics

Clinical biotechnology is the branch of biotechnology with direct application in hospital/ clinical scenarios on actual human patients rather than on laboratory or animal-based studies. Clinical Biotechnology includes clinical research, clinical trials, Clinical Studies carried out in the gene therapy, stem cell therapies, in humans, it also includes bio-medical applications such as devices for patient monitoring, treatment etc.

Clinical bioinformatics is an area of healthcare science responsible for developing and improving methods for acquiring, storing, organizing and analyzing biological data that supports the delivery of patient care. Clinical Bioinformatics has been divided into 3 sectors Genomics Clinical Bioinformatics, Health related clinical bioinformatics, Physical sciences related Bioinformatics. Genomic Clinical Bioinformatics is the sector connects computing, biology and medicine; those working in this area generally come from a variety of backgrounds including biology, computer science, statistics and informatics. Health Science - Clinical Bioinformatics information analysis and computing, as well as clinical, biomedical or physical sciences. This unique combination will enable you to integrate into a clinical-health informatics environment. Bioinformatics in physical sciences involves network topologies, standards compliance and computer programming.

Track 7: Pediatric Clinical Research

Clinical researches carried out for the welfare of children who facing health issues, diseases, rare genomic conditions etc., is known as pediatric clinical research. Pediatric clinical research considered little complex study as the subjects are infants as the physician or researcher have to take note of the infant individuality, vulnerabilities, behavior, anatomy and developmental peculiarities additionally they have to take note of the difference reactions and to take note of their fundamental biological differences between adults and children. To be moral, analysts must acquire the full and willful educated assent of taking an interest human subject. On the off chance that the subject can't assent for him/herself, specialists can look for assent from the subject's lawfully approved agent. For a minor youngster this is commonly a parent or gatekeeper since as younger than 18 can't lawfully offer agree to take an interest in a clinical preliminary. This pediatric sector seems to be very peculiar and essential for our generations. this topic covers all the clinical researches carried out for children.

Track 8: Clinical Chemistry

Clinical Chemistry (otherwise called synthetic pathology, clinical natural chemistry or restorative organic chemistry) is the region of science that is for the most part worried about investigation of organic liquids for demonstrative and helpful purposes. It is a connected type of organic chemistry (not to be mistaken for therapeutic science, which includes fundamental research for medication advancement).

The order began in the late nineteenth century with the utilization of basic compound response tests for different parts of blood and pee. In the numerous decades since, different strategies have been connected as science and innovation have progressed, including the utilization and estimation of catalyst exercises, spectrophotometry, electrophoresis, and immunoassay. There are currently many blood tests and clinical pee tests with broad symptomatic capacities.

Track 9: Clinical research in Microbiology and Clinical Pathology

Clinical Microbiology is the study of microbes like virus, bacteria, fungi, protozoa, which causes the infection and illness in humans and other living creatures. Clinical microbiology is the study of disease origination, development, transmission and their effects in humans. With this study they can able to formulate the medicine and drugs to treat these epidemic diseases. Formulated drugs will undergo clinical trials in 4 phases and their adverse reactions also recorded. With these researches it will take almost 10 years to reach the actual market.

Clinical pathology supports the diagnosis of disease using laboratory testing of blood and other bodily fluids, tissues, and microscopic evaluation of individual cells. Clinical pathology is itself divided into subspecialties, the main ones being clinical chemistry, clinical hematology/blood banking, hematopathology and clinical microbiology and emerging subspecialties such as molecular diagnostics and proteomics. This session deals with undergoing clinical researches in Microbiology and pathology to prevent and treat the epidemic and no epidemic diseases in a short period of time.

Track 10: Design of Clinical Studies & Clinical Trials

Clinical examination configuration is the plan of preliminaries and trials, and also observational examinations in therapeutic, clinical and different kinds of research (e.g., epidemiological) including human beings. The objective of a clinical report is to evaluate the wellbeing, viability, and/or the system of activity of an investigational restorative item or methodology, or new medication or gadget that is being developed, yet possibly not yet endorsed by a wellbeing specialist (e.g. Sustenance and Drug Administration). It can likewise be to explore a medication, gadget or technique that has just been endorsed however is still needing further examination, normally as for long haul impacts or cost-adequacy.

Track 11: Clinical Immunology & Clinical Oncology

Clinical Immunology & oncology is the session covers the undergoing clinical researches and clinical trials in cancer and immune system. Clinical immunology is the study of diseases caused by disorders of the immune system (failure, aberrant action, and malignant growth of the cellular elements of the system). It also involves diseases of other systems, where immune reactions play a part in the pathology and clinical features. Immuno-Oncology is the study carried to find the innovative ways to treat or destroy the cancer cells by activating the immune responses. This study involves the novel drug delivery systems with help of nano-medicine to induce the immune system. This type of inducing will help the body to destroy cancer cells naturally without making much destruction to healthy cells. This type of treatment considered to be very effective and less harmful, as traditional treatments like chemotherapy, radiotherapy etc., make the human system weak and prone to other diseases. As per the clinical market analysis many researches are under clinical trials and it also leads to effective cancer treatment methods which will enhance the health of our society.

Track 12: Clinical Cardiology & Clinical Psychology

Clinical Cardiology is the sector that treats the heart related health issues and taking steps to prevent cardiac diseases. According to the statistical studies About 92.1 million American adults are living with some form of cardiovascular disease or the after-effects of stroke. Direct and indirect costs of total cardiovascular diseases and stroke are estimated to total more than $329.7 billion; that includes both health expenditures and lost productivity. Clinical psychology is an integration of science, theory and clinical knowledge for the purpose of understanding, preventing, and relieving psychologically-based distress or dysfunction and to promote subjective well-being and personal development.

 This session covers the clinical researches and clinical trials in both cardiology & psychology which includes researches in treatment, genomic studies, adverse effects, health issues, behavioral studies, Genomic transmission, Psychological problems etc.

Track 13: Clinical Toxicology

Clinical toxicology is a sub specialty of medicine focusing on toxicology and providing the diagnosis, management, and prevention of poisoning and other adverse effects due to medications, occupational and environmental toxicants, and biological agents. Clinical toxicologists are involved in the assessment and treatment of a wide variety of problems including acute or chronic poisoning, adverse drug reactions (ADRs), drug overdoses, envenomation, substance abuse, industrial accidents, and other chemical exposures. Clinical Research in Toxicology discovers the science behind the toxic nature of drugs, medicines, or any other chemical substances which leads to the formulation of generic medicines and treatments. This session covers researches and their outcomes in toxicology.

Track 14: Pharmacodynamics & Pharmacokinetics

Pharmacodynamics is the study of how a drug affects an organism, whereas pharmacokinetics is the study of how the organism affects the drug. Both together influence dosing, benefit, and adverse effects. Pharmacodynamics is sometimes abbreviated as PD and pharmacokinetics as PK, especially in combined reference (for example, when speaking of PK/PD models). Pharmacokinetics is a branch of pharmacology dedicated to determining the fate of substances administered to a living organism. The substances of interest include any chemical xenobiotic such as: pharmaceutical drugs, pesticides, food additives, cosmetics, etc. It attempts to analyze chemical metabolism and to discover the fate of a chemical from the moment that it is administered up to the point at which it is completely eliminated from the body. This session deals with researches to find the effects of drug, medicine or treatment.

Track 15: Clinical Studies in Drug Delivery

Regardless of the ongoing advances in innovation to advance the assimilation, circulation, digestion and end (ADME) properties of new and promising restorative items to diminish clinical disappointments, the examination of medication mien in the pediatric and elderly populaces keeps on being under assessed. With the expanding predominance of maturing populaces around the world, there is a developing worry from medicinal services suppliers, controllers and the overall population that medication conveyance is still not as much as ideal for the defenseless patient populaces prone to be touchier to antagonistic impacts of the new investigational drugs. This survey of the database uncovered a quickly expanding number of clinical preliminaries and a pattern towards more extensive incorporation criteria of the elderly populace in clinical preliminaries in the course of recent years. In any case, when we condensed preliminaries by medication conveyance, organic stages, and infection classes, under 10% of these preliminaries included pharmacokinetic assessment in elderly subjects more prominent than 65 years old, and under 4% included pharmacokinetic assessment in youngsters under 17 years old. Over the different malady regions, the level of preliminaries that included pharmacokinetic assessment in the kids and elderly has stayed low and is reliably not as much as the examinations that incorporated the more youthful 18 to 65 age gathering. Accordingly, it isn't known whether the correct data is being produced from the developing number of clinical preliminaries to control ideal dosing proposals in exceptional patient populaces.

Track 16: Clinical Research in Nano Medicine

Nanomedicine is a generally new and quickly advancing field consolidating nanotechnology with the biomedical and pharmaceutical sciences. Nanoparticles (NPs) can grant numerous pharmacokinetic, adequacy, security, and focusing on advantages when they are incorporated into medication formulations. Many nanodrugs have entered clinical practice, and much more are being researched in clinical preliminaries for a wide assortment of indications. However, Nano pharmaceuticals additionally confront challenges, for example, the requirement for better portrayal, conceivable poisonous quality issues, an absence of particular administrative rules, cost– advantage contemplations, and winding down excitement among some social insurance experts. For these reasons, assumptions about nanodrugs that are in beginning times of improvement or clinical preliminaries need to remain realistic.

Track 17: Vaccine and Antibiotic clinical Research

Vaccine clinical research is the study carried out to develop a vaccine molecule or drug that acquires immunity against the particular disease. Antibiotic clinical research is the research carried to check the efficacy of antibiotics against the disease and to compare the effectives with existing medicines, efficacy can be calculated with the help of pre-clinical studies and clinical trials There is a developing thankfulness for the job of immunizations in standing up to the issue of antimicrobial obstruction (AMR). Immunizations can decrease the pervasiveness of opposition by lessening the requirement for antimicrobial utilize and can diminish its effect by decreasing the aggregate number of cases. By diminishing the quantity of pathogens that might oversee a specific clinical disorder, antibodies can allow the utilization of smaller range anti-microbials for exact treatment. These impacts might be opened by crowd insusceptibility, stretching out insurance to unvaccinated people in the populace. Since much choice for opposition is because of determination on observer individuals from the typical vegetation, immunization can diminish weight for obstruction even in pathogens excluded in the antibody. A few immunizations have effectively affected medication safe heredities inside the objective species, an advantage that could be even more intentionally misused in antibody plan. We portray the impacts of current immunizations in controlling AMR, study a few antibodies being developed with the possibility to do as such further, and examine procedures to open these advantages. We finish up with a talk of research and approach needs to even more completely enroll immunizations in the fight against AMR.

Track 18: Clinical Nursing & Nutrition

Clinical nursing research sessions provides an opportunity to discuss the advanced clinical practices and to know more about the efficacy of the drug among the population Clinical nourishment is sustenance of patients in social insurance. Clinical in this sense alludes to the administration of patients, including outpatients at facilities, as well as (and chiefly) inpatients in healing centers. It fuses basically the logical fields of sustenance and dietetics. It expects to keep a solid vitality balance in patients, and in addition giving adequate sums different supplements, for example, protein, vitamins, minerals.

Track 19: Public Health & Health Care

Public health is the expertise area of preventing disease, prolonging life and promoting human health through various efforts of society, organizations, both public and private, communities and individuals", while healthcare is the maintenance or improvement of health via the prevention, diagnosis, and treatment of disease, illness, injury, and other physical and mental impairments in human beings. Analyzing the health of a population and the threats is the basis for public health. Constant researches are going on to improve the health of the population and to prevent from infectious diseases. Clinical researches carried out to develop the medications and drugs to treat and to prevent (vaccines) are discussed under this topic.

Track 20: Clinical Ethics and Clinical Statistics

Clinical ethics is a system of moral principles that apply values to the practice of clinical medicine and in scientific research. Clinical ethics depends upon the conviction that, notwithstanding when perplexity is extraordinary, and feelings run high, doctors and attendants, patients and families can work helpfully to distinguish, break down and resolve a significant number of the moral issues that emerge in clinical solution. Clinical ethics is a practical discipline that provides a structured approach to assist physicians in identifying, analyzing and resolving ethical issues in clinical medicine.

Clinical statistics deals with applications of statistics to medicine and the health sciences, including epidemiology, public health, forensic medicine, and clinical research. Statistics play a distinct role in any clinical trial from design, conduct, analysis, and reporting in terms of controlling for and minimizing biases, confounding factors, and measuring random errors. Clinical research involves investigating proposed medical treatments, assessing the relative benefits of competing therapies, and establishing optimal treatment combinations. Statistical methods provide formal accounting for sources of variability in patients’ responses to treatment. With the recorded statistics in clinical trials, allows the clinical researcher to form reasonable and accurate inferences from collected information, and sound decisions in the presence of uncertainty. Clinical Statistics is the science of summarizing, collecting, presenting and interpreting data in medical practice, and using them to estimate the magnitude of associations and test hypotheses. Clinical statistics has a central role in medical investigations.

Track 21: Latest technologies in Biomedical Research

An incorporated approach utilizing compound, scientific and PC reenactments, in vitro tests, entire creature models, and human epidemiological examinations and clinical trials is right now the best way to deal with propel science, grow new items and medications, and treat, cure and anticipate sickness. Concoction, mechanical, numerical and PC recreations demonstrate most valuable in the preparatory phases of research where they can fortify thoughts regarding new research bearings. These are compelling examination models yet they can't supplant research center testing. PC reproductions are a successful research instrument since they increment speed and effectiveness of existing information. Human examinations include taking research center information on the security and adequacy of new immunizations or solutions and assessing them in precisely arranged clinical trials utilizing educated human volunteers. At the point when people are utilized as a part of biomedical research contemplates drugs are normally tried

  • Animal Models for Human Diseases
  • The Ethical Basis for Animal Use in Research
  • Databases for Biomedical Animal Resources
  • Improved Models for Animal Research

Track 22: Clinical Trials in Developing Countries

Clinical research concentrates that investigate whether a restorative methodology, treatment, or gadget is protected and successful for people. Ponder indicate which medicinal methodologies work best for specific sicknesses or gatherings of individuals. The reason for clinical trials is research, so the reviews take after strict logical gauges. These guidelines secure patients and deliver dependable review comes about. Clinical research is one of the last phases of a long and cautious research handle. Clinical trials are directed for each malady. The primary purpose behind doing trials is to figure out if one treatment is superior to another, 19% by and large increment in number of enlistment every year in Clinical Trials, 47.0% expansion in Market Investment in Clinical Trials from 2013-2015

  • Asia Clinical Trials
  • Globalization of Clinical Trials
  • Canada Clinical Trials
  • Japan Clinical Trials
  • Europe Clinical Trials
  • USA Clinical Trials
  • UK Clinical Trials

Track 23: Clinical Trials on Different Diseases

Clinical Trials for various infections and clutters are led for assessing at least one medication (for instance, drugs, restorative gadgets, and ways to deal with surgery or radiation treatment) for treating a malady, disorder, or condition furthermore discovering approaches to keep the underlying advancement or repeat of an ailment or condition. These can incorporate meds, immunizations, or way of life changes, among different methodologies. A diabetes prevention clinical research is testing whether a successful, but expensive, hospital-based strategy of identifying people with pre-diabetes and helping them lose weight can be adapted to be delivered at the community level, using peer-led interventions

  • Research and Trials on Human Cells
  • Research in Pathology
  • Research and Studies on wounds and injuries
  • Clinical trials on rare diseases
  • Medical Devices Clinical Trials

Track 24: Bioethics and Regulatory Compliance

Bioethics is the investigation of the commonly questionable moral issues rising up out of new circumstances and potential outcomes realized by advances in medication. It is additionally moral insight as it identifies with therapeutic approach, practice, and research. Bioethicists are worried with the moral inquiries that emerge in the connections among life sciences, biotechnology, prescription, clinical research, and reasoning and so forth. One of the principal ranges tended to by present day bioethicists was that of human experimentation. The National Commission for the Protection of Human Subjects of Biomedical and Behavioural Research was at first settled in 1974 to recognize the fundamental moral rule that ought to underlie the lead of biomedical and behavioural research including human subjects.

Clinical research morals are the arrangement of significant morals considered in the direct of a clinical trial in the field of clinical research. It acquires from the more extensive fields of research morals and restorative morals. Nature of clinical trials relies on upon information respectability and subject security. Globalization, outsourcing and expanding multifaceted nature of clinical trials have made the objective of accomplishing worldwide quality testing. The quality, as judged by administrative assessments of the examiner locales, supports/contract inquire about associations and Institutional Review Board, has been of worry to the US Food and Drug Administration, as there has been not really any adjustment in recurrence and nature of basic insufficiencies. Great Clinical Practice (GCP) is the general moral and logical quality standard for leading clinical trials. The GCP standard applies to all parts of the clinical trial.

  • Ethics & Human Subject Protection
  • Ethical and regulatory issues
  • Compliance and regulatory requirements in clinical research
  • Regulatory Inspections of Research Sites
  • Techniques for designing case report forms in clinical research

Track 25: Future of Clinical Trials

The eventual fate of clinical research showed as takes after. Get to and connect with the patient online – Attract patients to the trial – Consent patients and change over to subjects – Remotely oversee subjects and gather information. The support arrangements to draw in the patient through online networking, for example, Facebook, and standard email overhauls keeping in mind the end goal to pull in the patient to the trial, and once the patient consents to take in more about the trial, the support sends the patient a bundle containing portable wellbeing gadgets, which gather restorative demonstrative information and sends that information to the support. The patient turns on the tablet, which contains an electronic assent and a video of a doctor clarifying the clinical trial in detail. Refinement in computerized media is accepted to be a powerful instrument that is utilized to speak with patients. Amid the clinical trial, the subject can get to live doctors either for all intents and purposes or through adjacent restorative group focuses.

Remote medical caretakers visit the subject at their homes to gather tests. What's more, the patient uses the portable wellbeing gadget to naturally transfer think about information specifically to the support's EDC database. Recent advances in clinical research have enabled to understand the molecular basis of disease. Equally important, a growing suite of biomarkers now provides predictive value for diagnosis and prevention/remission. Clinical research techniques are targeting new sources of information from patients, recognizing the uniqueness of individual subjects and producing massive quantities of data. Clinical research toolbox has grown so extensively that the research community is no longer limited

  • Embracing the clinical trial of the future
  • Designing the clinical trial of the future
  • Cloud based medical image management for clinical trials
  • Clinical development of the future
  • Clinical trial site of the future
  • Mobile technology
  • Paperless Clinical Trials

Track 26: Patient Recruiting & Retention

Enlisting and selecting patients for clinical trials can frequently be a long and troublesome process. It's not shocking at that point, that finding the objective statistic, qualifying and selecting patients can expend significant time and cash. Hence, it is basic that the way toward enrolling is all around arranged and fits inside the convention spending plan and timetable. When patients are enlisted in an examination, it can be similarly as difficult to hold them. An assortment of startling variables can lead patients to pull back from the examination, bringing about insufficient information and conceivably, a costlier trial. Before you set out on a patient enlistment crusade, it is vital to have an arrangement. Taking a gander at your accessible assets, doing your examination, and defining objectives can enable spare to time and cash over the long haul. The best and minimum costly patient to select into an examination originates from the site's own particular database or practice. These patients as of now have an association with the site, know about their examination, and have been most agreeable while taking an interest in investigate. Consequently, setting the site up for viable inside enlistment through enrolment arranging is imperative to the accomplishment of any investigation.

  • Informed Consent
  • Purpose of the Manual of Procedures
  • MOP Template and Mechanics
  • Safety definitions for clinical research





Media Partners/Collaborator

A huge thanks to all our amazing partners. We couldn’t have a conference without you!


A huge thanks to all our amazing partners. We couldn’t have a conference without you!