Webinar on Clinical Trials welcomes all the professionals to the virtual meeting on July 20, 2022 in London, UK (time zone). The theme of the webinar is Clinical Trials: Research for a better and consistent future.
Clinical Trials 2022 focus on various disciplines involved in the pre-clinical research and conduct of clinical trials. It promotes better understanding by the general public about the importance of clinical trials in the prevention, diagnosis and treatment of disease. It is the best platform to encourage the sincere administration of medication by various procedures for various ailments with evidence and providing the righteous option for treating ailments.
Session 1: Innovations in Clinical Trials
Clinical trials for the possibilities of new remedies and their most part started and financed by industry. There are various clinical trials initiated by clinical professionals. Clinical research is frequently performed all over the world, which can now and then, be expansive ones. As an outcome, clinical research is exceedingly controlled.
Session 2: Pre-clinical Research
Pre-clinical research is a stage of research that begins before clinical trials and during which important feasibility, iterative testing and drug safety data are collected, typically in laboratory animals. The main goals of pre-clinical research are to determine a starting, safe dose for first-in-human study and assess for the potential toxicity of the product, which typically include new medical devices, prescription drugs, and diagnostics.
Session 3: Clinical Trials on Different Diseases
Clinical Trials for different diseases leads to assessing at least one medication for treating a disorder or a condition. Discovering approaches to keep the underlying advancement or continuous ailments or conditions. These can incorporate immunizations or way of changes among various aspects.
Session 4: Pharmacovigilance and Drug Safety
Pharmacovigilance is the pharmacological science relates to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. 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.
Session 5: Latest technologies in Clinical Research
Technology plays a critical role in drug development and the R&D value chain by revolutionizing clinical trials and decreasing the failure rate. Though the supply of technology has been increasing and regulation of innovative methods is easing, pharmaceutical companies have been slow to use the emerging technologies, due to the ambiguity prevailing around this space and a highly fragmented supply market.
Session 6: Clinical and Medical Case Reports
A case report is a detailed report of the symptoms, signs, diagnosis, treatment, and follow-up of an individual patient. Case reports may contain a demographic profile of the patient, but usually describe an unusual or novel occurrence. Some case reports also contain a literature review of other reported cases. Case reports are professional narratives that provide feedback on clinical practice guidelines and offer a framework for early signals of effectiveness, adverse events, and cost.
Special session on Pediatric nutrition: Pediatric nutrition considers the dietary needs of infants to support growth and development, including changes in organ function and body composition.
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