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23rd World Congress on Toxicology and Pharmacology, will be organized around the theme “Probing novel facts in Toxicology and Pharmacology”

Toxicology Congress 2021 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Toxicology Congress 2021

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Toxicology is the qualitative and quantitative study of the adverse effects of chemicals and other materials on living organisms. The dose of the substance is an important factor in toxicology, as it has a relationship with the effects on the individual. Factors that influence toxicity include the dose, the route of exposure, shape and structure of the chemical, the species, individual human factors and environment. Toxicology and Pharmacology are both studies that involve in assessing the properties of chemicals and their actions on the body, but differ significantly in other areas. Pharmacology focuses on the therapeutic effects of pharmaceutical substances and how they can be used most effectively for medical purpose. Whereas, toxicology is closely related to the adverse effects that can occur in living organisms that come into contact with chemical compounds. Toxicologists are also concerned with determining the risk of certain substances with risk assessment tools.

  • Track 1-1Clinical toxicology
  • Track 1-2Geriatric toxicology
  • Track 1-3Pediatric toxicology
  • Track 1-4Drug and chemical toxicology
  • Track 1-5Comprehensive toxicology
  • Track 1-6Organ toxicity
  • Track 1-7Neurotoxicology and Teratology
  • Track 1-8Systemic toxicology
  • Track 1-9Predictive toxicology

Risk assessment includes the characterization of the uncertainties inherent in the process of inferring risk. Toxicology data helps to determine the risk of exposure to certain chemicals. The practices of risk assessment are used to assess the related health risks to provide a scientific basis for regulatory standards development and risk management decision making for human health protection. The presence of chemicals in our environment is a subject of deep interest owing to the many potential adverse health effects to humans following exposure to these chemicals. The validity of an estimation of risk derived from a risk assessment depends greatly on the quality and accuracy of data. Where data do not exist or are contradictory, regulatory agencies are required to rely on default values, uncertainty factors, and modeling approaches to fill in the blanks. These defaults and extrapolations introduce uncertainty into the risk estimates. New methodologies and testing methods could fill key data gaps, clarify data inconsistencies, or otherwise reduce uncertainty. If applied appropriately, these approaches have the potential to improve the accuracy and scientific credibility of regulatory decision making. Human health risk assessment is the process of investigating information to determine whether an environmental hazard might cause harm to exposed persons. The risk-assessment process incorporates many disciplines of Toxicology.

  • Track 2-1Safety evaluation, risk and hazard assessment
  • Track 2-2Chemical research in toxicology
  • Track 2-3Regulatory toxicology
  • Track 2-4Computational toxicology
  • Track 2-5Toxicokinetics and Toxicodynamics

Analytical toxicology laboratories may be involved in activities such as the assessment of exposure following chemical incidents, therapeutic drug monitoring, monitoring the drugs of abuse and forensic analyses. They may also be involved in research like determining the pharmacokinetic and toxicokinetic properties. Liquid chromatography-mass spectrometry and Gas chromatography-mass spectrometry are generally used today in analytical toxicology. While planning the development of an analytical toxicology service there are a number of considerations. These comprise the pattern of poisoning and, therefore, the specific substances for which analyses will be required, the existing infrastructure, the availability of ongoing technical support, spare parts and reagents from suppliers, the availability of a team of trained staff and the capacity to train new staff and provide continuing professional development.

  • Track 3-1Animal testing methods
  • Track 3-2Alternative testing methods
  • Track 3-3Drug discovery, development and evaluation
  • Track 3-4In vitro toxicity testing
  • Track 3-5Pre-clinical toxicity testing

In Genotoxicity testing, to assay for genotoxic molecules, researchers assay for DNA damage in cells exposed to the toxic substrates. Techniques like in vitro and in vivo Toxicology Tests, Ames Assay and Comet Assay have been developed to determine the chemical’s potential to cause DNA damage that may lead to cancer. Genotoxicity tests are designed to detect drugs which can cause genetic damage directly or indirectly by various mechanisms of action. Compounds which are identified as genotoxic in these tests have the ability to be human carcinogens and ultimately may induce cancer and heritable defects. Genotoxicity testing of new chemical entities is an integral part and is a regulatory requirement prior to the approval of new drugs, in Drug Development process. Late stage failures can be reduced by identifying genotoxicity at an early stage in Drug Discovery rather than during regulatory assessment.


  • Track 4-1Genotoxic drugs
  • Track 4-2Genotoxicity testing
  • Track 4-3In vitro and in vivo testing
  • Track 4-4Pharmacogenetics & pharmacogenomics
  • Track 4-5Genotoxicity and mutagenicity

The primary concern of Forensic Toxicology is to obtain and interpret the results. Toxicological analysis can be done to various kinds of samples. Forensic toxicology involves not only determining the presence of Toxic substance in the post-mortem body, but how the body’s natural processes affect the substance, including chemical change and dilution. Forensic toxicologists perform scientific tests on tissue samples and bodily fluids to identify any chemicals or drugs present in the body. The choice of method for testing is highly depends on the material on which the testing is performed and what kind of substance one expects to find. Analytical methods used in forensic toxicology should be carefully tested by performing a validation of the method to ensure definite results at all times. Forensic toxicologists also work on cases involving environmental contamination, to determine the impact of chemical spills on living organisms. Investigators rely on the forensic toxicologist to make reliable conclusions about the impact a specific amount of a specific substance would have on a specific individual. Currently, forensic toxicology is the study of drugs, alcohol and poisons, including their chemical composition, identification and preparations. It comprises knowledge about the absorption, distribution and elimination process of such substances in the body, as well as the manner in which the body responds to their presence and the factors which define Drug Safety and efficacy.

  • Track 5-1Forensic samples for toxicology testing
  • Track 5-2Forensic toxicology applications
  • Track 5-3Challenges in forensic toxicology
  • Track 5-4Forensic toxicology today
  • Track 5-5Post-mortem Forensic Toxicology

Food safety includes the origins of food including the practices relating to food labelling, food additives, pesticide residues and food hygiene as well as policies on Biotechnology and food. Food can transmit disease from person to person as well as help as a growth medium for bacteria that can cause food poisoning. In developed countries there are sophisticated standards for food preparation, whereas in lesser developed countries the main issue is simply the availability of sufficient safe water, which is usually a critical item.  Harmful effects of biological and chemical agents can include toxicants from pesticides, pollutants, fertilizers and insecticides all of which can impact an organism and its population through shifts in species diversity and abundance contributing to Environmental Toxicology.

Living organisms can be exposed to Toxicants at various stages of their life cycle. The amount of toxicity can vary depending on where the organism is found within its food web.


  • Track 6-1Food safety and food allergies
  • Track 6-2Risk assessment of chemicals in food
  • Track 6-3Environmental and occupational health
  • Track 6-4Particle and fibre toxicology
  • Track 6-5Industrial and metallic toxicology
  • Track 6-6Plant toxicology
  • Track 6-7Aquatic Toxicology
  • Track 6-8Food Toxicology
  • Track 6-9Veterinary Toxicology

The development of novel drugs requires non-clinical safety studies to be performed on candidate drug compounds. Such studies typically assess general toxicology safety pharmacology and Genetic Toxicity test batteries. These studies notify development of candidate drugs from the “discovery phase” through clinical development to regulatory submission and registration. Less importance was placed on the evaluation of safety issues for projects while still in the drug design phase. Therefore, this led to a number of major failures of candidate drugs in early development due to toxicological issues. In response to this costly attrition, many pharmaceutical companies have now dedicated in “Discovery-phase Toxicology” or “Discovery Safety” to detect likely hazards and to take steps to design out or significantly reduce unwanted properties at an earlier stage, with the ultimate aim of improving the probability of success in non-clinical and clinical drug development.


  • Track 7-1Nanotoxicology
  • Track 7-2Innovations in applied toxicology and toxicological sciences
  • Track 7-3Emerging in-vitro models for the toxicity studies
  • Track 7-4Developmental and reproductive toxicology
  • Track 7-5Application of toxicology in drug development

Experimental toxicology results in more number of drug reactions which we come across during practical session. The animals which are used in experimental purpose are given drugs at different doses to know the drugs bioavailability, pharmacokinetics, pharmacodynamics and their functions on various temperatures. The in vivo and in vitro are the two major studies which help in practical study.


  • Track 8-1Toxicologic pathology
  • Track 8-2In Vitro and In Vivo mechanisms
  • Track 8-3Xenobiotic Risk Characterization

Some of Medical and Clinical Toxicology encounters are Unintentional and intentional overdoses, Exposure to industrial chemical products and environmental hazards, Drug abuse management, Diagnosis and management of exposures and Independent medical examinations, assessing injury or disability resulting from toxic exposures.

  • Track 9-1Drugs of abuse
  • Track 9-2Unintentional and intentional overdoses
  • Track 9-3Evaluation of chemically induced diseases
  • Track 9-4Pre-Clinical toxicology studies

We live in the most modernized and industrialized world where we get exposed to the number of the chemicals and toxic substances which cause severe damage to the body and the environment. In this part the industrial workers are widely exposed to the chemicals which cause severe damage to the body. The industrial toxicology deals with the safety of workers and the various steps to be taken to prevent the bioaccumulation of the heavy metals.


Toxicology testing, also known as safety assessment, or toxicity testing, is conducted to determine the degree to which a substance can damage a living or non-living organisms. Toxicity tests examine finished products such as pesticides, medications, cosmetics, food additives such as artificial sweeteners, packing materials, and air freshener, or their chemical ingredients. The substances are applied to the skin or eyes; injected intravenously, intramuscularly, or subcutaneously; inhaled either by placing a mask over the animals.

  • Track 11-1In vitro toxicity testing
  • Track 11-2Toxicity testing in preclinical development
  • Track 11-3Toxicity evaluation
  • Track 11-4Toxicological screening methods
  • Track 11-5Experimental toxicology
  • Track 11-6Human toxicology

Pharmacological studies involve examining the interactions between chemical substances and living systems, with a view to determining the properties of drugs and drug actions, including the drug molecules and drug receptors interactions and how these interactions elicit an effect. The study of chemicals requires good knowledge of the biological system affected. With the knowledge of biochemistry and cell biology increasing, the field of pharmacology has also changed significantly. It is now possible to design chemicals that act on specific cellular signaling or metabolic pathways by affecting sites directly on cell-surface receptors, through molecular analysis of receptors.


  • Track 12-1Clinical pharmacology
  • Track 12-2Biochemical pharmacology
  • Track 12-3Neuropharmacology
  • Track 12-4Psychopharmacology
  • Track 12-5Respiratory pharmacology
  • Track 12-6Pediatric pharmacology
  • Track 12-7Geriatric pharmacology

Applied pharmacology is the study of how drugs affect body. Drugs can be used to both maintain a healthy lifestyle and treat or cure disease. It also provides explanation for different drugs having connected with the pharmacological action. It gives clarifications about drug interactions and the action of various drugs on the many organs in the body when they are in diseased state with side effects contradictions.


  • Track 13-1Molecular and cellular pharmacology
  • Track 13-2Nanomedicine in pharmacology
  • Track 13-3Pharmacological testing
  • Track 13-4Behavioral pharmacology
  • Track 13-5Clinical application of systems pharmacology models

Pharmacological Testing includes both Pharmacologic stress testing and nuclear stress test. Whereas the Pharmacologic stress testing is the set up after activity testing, is an analytic system in which cardiovascular anxiety affected by pharmacologic operators is shown in patients with diminished useful limit or in patients who can't work out. And Pharmacological nuclear stress test is a demonstrative test used to assess blood stream to the heart. Amid the test, a little measure of radioactive tracer is infused into a vein. A unique camera, called a gamma camera, identifies the radiation discharged by the tracer to create PC pictures of the heart.

  • Track 14-1In vitro and In vivo models
  • Track 14-2Randomized controlled clinical trials
  • Track 14-3Pharmacokinetics
  • Track 14-4Pharmacologic stress testing
  • Track 14-5Drug reaction testing

Cardiovascular Pharmacology understanding of not only general pharmacologic principles and mechanisms of action of cardiovascular drugs, but more importantly, with an understanding of the rationale for drug use.


  • Track 15-1Heart diseases and failure
  • Track 15-2Cardiovascular pharmacotherapies, cardiac procedures and surgeries
  • Track 15-3Risk factors for cardiovascular diseases
  • Track 15-4Interventional cardiology
  • Track 15-5Nuclear cardiology and echocardiography
  • Track 15-6Cerebrovascular heart diseases
  • Track 15-7Diseases associated with cardiovascular diseases
  • Track 15-8Heart diseases in different rationale

Medicine Development includes many new medications or chemicals which may influence the strength of people are required by law to be tried on creatures. The safety tests provide data for arranging human trials; speak to a little extent of the advancement procedure for another medication. The tests can't anticipate the greater part of the responses a human may have to a given substance, more extensive inquiries concerning impacts on the heart, liver, lungs or skin are replied through creature concentrates so that its relative danger is known. Intense poisonous quality tests, where a solitary, high dosage of a substance is given to creatures, are performed right off the bat being developed.

  • Track 16-1Pharmacodynamics and pharmacokinetics
  • Track 16-2Ethical and legal issues
  • Track 16-3Drug screening and discovery
  • Track 16-4Drug-drug interactions
  • Track 16-5Pharmacovigilance