World Pharmacology Congress 2019

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The Pharmaceutical industry is directly impacted by the research conducted with prescription vaccines, OTC drugs and drugs being manufactured based on findings from the examine of lifestyles sciences. Medical trials are conducted to ensure that products being evolved are tested on how well they work on individuals affected by the conditions or diseases they are created to treat.

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Clinical pharmacology is a branch of biomedical science. It consists of drug discovery, the study of the effects of drugs on their targets in living systems and their clinical use, as well as the study of biological function related to these chemicals. Clinical pharmacology includes application of pharmacological principles, such as pharmacokinetics and pharmacodynamics.

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Pharmacogenomics is the study of how our DNA impacts our response to different medications. DNA contains our genetic code and serves as the blueprint for building the cells of the human body. All of us have small differences, or variants, in our DNA that make each of us specific. Few are germline variants and others somatic variants are acquired throughout life, frequently due to environmental factors. Our distinctive genetic makeup often way that a one-size-fits-all method to drug treatment might not be most reliable. Humans receiving the same medication at the same dose for the same health condition may have vastly different experiences.

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Pharmacokinetics is presently defined as the study of the time course of drug distribution, absorption, excretion and metabolism. Clinical pharmacokinetics is the utility of pharmacokinetic ideas to the safe and effective therapeutic management of drugs in an individual patient. Primary goals of scientific pharmacokinetics include enhancing efficacy and decreasing toxicity of a affected person's drug therapy. The development of strong correlations between drug concentrations and their pharmacologic responses has enabled clinicians to use pharmacokinetic principles to real patient conditions.

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Pharmacoepidemiology is the study of the utilization and effects of drugs in large numbers of humans. It provides an estimate of the probability of beneficial results of a drug in a population and the chance of negative effects. It can be called a bridge science spanning both epidemiology and clinical pharmacology. Pharmacoepidemiology concentrates on medical affected person consequences from therapeutics through the usage of techniques of medical epidemiology and applying them to expertise the determinants of beneficial and detrimental drug effects, effects of genetic variation on drug effect, period-response relationships, medical effects of drug-drug interactions, and the consequences of medicine non-adherence.

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The word posology is derived from the Greek (Poses- how much and logos- science) is the branch of pharmacology dealing with doses. This depends upon various factors including age, climate, weight, sex, and elimination rate of drug, genetic polymorphism and time of administration.

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Neuropharmacology is the study of the effects of drugs on the nervous system, with the aim of growing compounds that offer therapeutic benefit in human beings with neurological disease and psychiatric . We consider that an understanding of a drug's action requires an integrated knowledge of the cellular and molecular mechanisms by which the drug exerts its effects upon brain circuitry and ultimately human behavior.

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Psychopharmacology refers to the study of drugs and the effects it has on mood, wondering, conduct and sensation. It brings collectively psychology, neurology, chemistry, and other different stem fields with the intention to construct a specialized field that makes a speciality of studying what drugs are helpful for people who are trying to keep intellectual health conditions.

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Pediatric Pharmacology basically concerns around the investigation of medication activity in children. All the more particularly, it is the investigation of the distinctive impacts which seems with the utilization of medication in the variety of age groups like neonate, preterm, child, infant and adolescent. This examination likewise demonstrates age related pharmacokinetic contrasts in children contrasted with grown-ups. Pediatric Pharmacology plans to distribute discover devoted in particular to fundamental, translational and clinical pharmacology in children.

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Toxicology is the study of chemicals that can cause issues for living things. It's a wide-ranging field. The chemicals may occur naturally or created in a lab or factory. The living things may be human beings, pets, livestock, or microbes living in a pond. And the issues that concern toxicologists stretch from inconvenience to disaster from mild skin irritation, for instance, to death.

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Theoretical pharmacology is a fairly new and hastily expanding discipline of research interest wherein the some of the strategies used to compute the electronic structures of disconnected and solvated drugs and biomolecules and their intermolecular co-operations are portrayed and their relative benefits or lacks assessed.

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Behavioral pharmacology, as an area, is closely intertwined with the experimental analysis of conduct, and, for that reason, relies closely on its methodology, concept and conceptual bases. In reality, it's far feasible to argue that had been it not for the experimental analysis of conduct there might be no research area called behavioral pharmacology.

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Environmental Pharmacology is a relatively new and rising distinctiveness of pharmacology. It involves the examine of gene-environment interaction, toxin-environment interaction and drug-environment interaction. It is important to emphasize at this stage that the different terms used interchangeable with environmental pharmacology include pharmacoenvironmentology ecopharmacology and ecotoxicology. Environmental Pharmacology entails the study of environmental science, chemistry, medicine, ecology and genetics.

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Drug delivery refers to formulations, technologies, systems and approaches for transporting a pharmaceutical compound in the body as needed to safely achieve its desired therapeutic effect. It is able to involve scientific site-targeting on inside the frame, or it would contain facilitating systemic pharmacokinetics. In any case, it is typically concerned with both duration and quantity of drug presence. Drug delivery is often approached thru a drug's chemical formulation. However it can also contain drug-device or medical devices combination products.

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The process of the discovery and design of drugs commonly involves understanding the character of targets related to the disorder, setting-up the concept of drug design, imparting lead compounds and design and lead optimisation by means of analysing structure-activity-relationships. A deep understanding of this process in addition to the mode of action at a molecular level will help pharmacists with decisions on appropriate dosing and management of drugs.

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Bioequivalence is a measure of comparability between dosage sorts of the identical drug and is used to determine whether the two drug products may be used interchangeably. Bioavailability is a size of the charge and quantity to which a therapeutically active chemical is absorbed from a drug product into the systemic circulate and will become to be had on the site of action.

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Adverse drug reactions are not unusual. Identifying authentic drug allergy reaction, but can be difficult. Complicating elements of drug reactions encompass the myriad clinical symptoms and multiple mechanisms of drug-host interaction, a lot of that are poorly understood. Similarly, the relative paucity of laboratory trying out this available for drug allergy makes the diagnosis dependent on clinical findings.

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Reproductive pharmacology is a branch of pharmacology which deals with the medicine that affects on reproductive system. Reproductive pharmacology is a large topic with application in all characteristics of reproductive and sexual health. Because of pharmacological interventions there are most of the upgrades in maternal and infant morbidity and mortality. Treatment of infertility indicates increasing success this is a growing enterprise which often now relies on specific pharmacological intervention

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Pharmacovigilance is part of pharmacoepidemiology that includes chronic monitoring, in a population, for unwanted results and different protection concerns arising in drugs which can be already available on the market. Pharmacoepidemiology occasionally also entails the behavior and evaluation of programmatic efforts to improve medication use on a population foundation. The function of Drug Safety can range depending on company length, type of products and many others. But they will normally contain series, detection, evaluation, monitoring, reporting and prevention of negative outcomes and following these statistics up with a report. In the end, Pharmacovigilance and Drug Safety are concerned with identifying the hazards associated with pharmaceutical products and with minimising the risk of any harm that may come to patients.

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Pharmaceuticals and personal care products include numerous chemical classes. Pharmaceuticals are used primarily to treat or prevent human & animal disease, whereas personal care products are used to improve the quality of daily life and include products such as, lipsticks, shampoos, hair colors, deodorants, toothpastes and moisturizers.

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Radiopharmaceuticals are the radioactive drugs or radioactive substances for therapeutic or diagnostic interventions. They may be given to the patient in different ways. However, when small amounts are used, the radiation human body receives from them is very low and is considered safe. When larger amounts of these agents are given to treat disorder, there may be different effects on the body. Some radiopharmaceuticals are used in larger quantities to treat certain kinds of cancer and other diseases.

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