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20th Medicinal & Pharmaceutical Sciences Congress, will be organized around the theme “Challenges and New ideas in Pharmaceutical and Medicinal Sciences”

Med Pharma Congress 2020 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Med Pharma Congress 2020

Submit your abstract to any of the mentioned tracks.

Register now for the conference by choosing an appropriate package suitable to you.

Medicinal chemistry or Pharmaceutical Chemistry mainly deals with the drug design, optimization and development of chemical compounds. This field includes multidisciplinary topic such as synthesis of potential drugs followed by studies investigating their interactions with biological targets to understand the medicinal effects of the drug, its metabolism and side-effects

  • Track 1-1Computational Chemistry and Chemical Biology
  • Track 1-2Molecular Stereochemistry
  • Track 1-3Pharmaceutical Biotechnology
  • Track 1-4Pharmaceutical Drug Impurities
  • Track 1-5Genesis of Novel Drugs
  • Track 1-6Drug Designing Methodologies
  • Track 1-7Green Chemistry in Pharma Industry
  • Track 1-8Diastereomers
  • Track 1-9Isomerism chemistry

Pharmacology is that the scientific study of drug action on biological systems. It is the study of the interactions between a living organism and drugs, defined as the branch of medicine concerned with the uses, effects, and modes of action of drugs

  • Track 2-1Immunopharmacology and Immunotoxicology
  • Track 2-2Psychopharmacology
  • Track 2-3Pharmacogenetics and Pharmacogenomics
  • Track 2-4Genetic and Molecular Toxicology
  • Track 2-5Pharmacotoxicology
  • Track 2-6Pharmacokinetics and Pharmacodynamics parameters
  • Track 2-7Cytochrome -P-450 inhibitors / inducers
  • Track 2-8Autacoids

Biopharmaceutical Science contains the study of the drug discovery and their development, and along with their properties, both physical and chemical. It conjointly deals with the biological effects of the medicine like onset and period of action beside their intensity within the body. Bio pharmaceutics facilitate in calculative the bio availability and therapeutic activity of the medicine within the body

  • Track 3-1Clinical Trials on Biopharmaceuticals Products
  • Track 3-2Biopharmaceutical Drug Design and Development
  • Track 3-3Quality Assurance and Quality Control
  • Track 3-4Drug binding and targeting
  • Track 3-5Drug delivery Systems
  • Track 3-6Bioavailability & Bioequivalence studies
  • Track 3-7Biopharmaceutical Pharmacovigilance
  • Track 3-8Clinical Trials and Research
  • Track 3-9Pharmaceutical Analysis
  • Track 3-10Biologics & Biosimilars
  • Track 3-11Pharmaceutics and Pharmacotherapeutics

Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patient. For orally administered drugs, this usually involves incorporating the drug into a tablet or a capsule. It is important to make the distinction that a tablet contains a variety of other potentially inert substances apart from the drug itself, and studies have to be carried out to ensure that the encapsulated drug is compatible with these other substances in a way that does not cause harm, whether direct or indirect.

  • Track 4-1Solid Dosage Forms
  • Track 4-2Semi-Solid Dosage Forms
  • Track 4-3Liquid Dosage Forms
  • Track 4-4Gaseous Dosage Forms
  • Track 4-5Parenteral dosage form
  • Track 4-6Novel Drug Delivery Systems
  • Track 4-7General Considerations in Dosage Forms
  • Track 4-8Drug Formulation Procedures
  • Track 4-9Drug absorption barriers
  • Track 4-10Pharmaceutical Excipients
  • Track 4-11Pharmaceutical Formulations Market

Pharmacovigilance is also known as drug safety, and it is  the practice of monitoring the effects of medical drugs after they have been licensed for use, especially in order to identify and evaluate previously unreported adverse drug reactions

  • Track 5-1Pre-Clinical and Clinical Trials
  • Track 5-2Adverse Drug Reactions
  • Track 5-3Pharmacovigilance and Risk Management
  • Track 5-4Good Pharmacovigilance Practice
  • Track 5-5Pharmacy Practices and its Challenges
  • Track 5-6Pharmacovigilance Significance & Scope
  • Track 5-7PV consulting and Business Opportunity

Ethno medicine is a study or comparison of the traditional medicine based on bioactive compounds in plants and animals and practiced by various ethnic groups, especially those with little access to western medicines, e.g., indigenous peoples. The word ethno medicine is sometimes used as a synonym for traditional medicine

  • Track 6-1Ethno pharmacology
  • Track 6-2Traditional Medicine
  • Track 6-3Phytochemical Studies of Plants and Plant Extracts
  • Track 6-4Herbal and Holistic medicine
  • Track 6-5Trends and Developments in Ethno pharmacology

Pharmaceutical analytical techniques explain the process or different processes to identify and quantify a substance, the components of a pharmaceutical solution or mixture or the determination of the structures of chemical compounds used in manufacturing of the pharmaceutical product. The components monitored include process impurities, chiral or achiral drugs, residual solvents, degradation products, excipients such as preservatives, extractable and leachable from container and closure or manufacturing process, pesticide in drug product from plant origin, and metabolites.

  • Track 7-1Analytical Chemistry
  • Track 7-2Bioanalysis
  • Track 7-3Pharmaceutical Analysis Errors and Validation
  • Track 7-4Spectroscopy and its techniques
  • Track 7-5Pharmaceutical and Biomedical Analysis
  • Track 7-6Electro chemical and Thermo Analytical Techniques

Pharmacoepidemiology is the study of the utilization and effects of drugs in large numbers of people; it provides an estimate of the probability of beneficial effects of a drug in a population and the probability of adverse effects. It can be called a bridge science spanning both clinical pharmacology and epidemiology. Pharmacoepidemiology concentrates on clinical patient outcomes from therapeutics by using methods of clinical epidemiology and applying them to understanding the determinants of beneficial and adverse drug effects, effects of genetic variation on drug effect, duration-response relationships, clinical effects of drug-drug interactions, and the effects of medication non-adherence.

  • Track 8-1Molecular pharmacoepidemiology
  • Track 8-2Pharmacogenetics and pharmacogenomics
  • Track 8-3Toxicology & toxicogenomic studies
  • Track 8-4Renal pharmacoepidemiology & adrenergic drugs
  • Track 8-5Pharmacoepidemiology in health-care and industry
  • Track 8-6Cancer pharmacoepidemiology and genomics
  • Track 8-7Pharmacokinetics and Pharmacodynamics

Phytochemistry is in the study of phytochemicals in plants and other natural sources. Phytochemicals are chemicals derived from plants. In other words the terms are often used to describe the large number of primary and secondary metabolic compounds found in plants. Phytochemicals have properties such as protection against insect attacks and diseases. They also exhibit a number of protective functions for human beings also.

  • Track 9-1Traditional Medicine
  • Track 9-2Clinical Pharmacognosy
  • Track 9-3Aromatic Medicinal Plants
  • Track 9-4Marine Drugs
  • Track 9-5Applied Plant Sciences

Pharmacogenomics is the study of how genes affect a person’s response to drugs. This relatively new field combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop effective, safe medications and doses that will be tailored to a person’s genetic makeup.

  • Track 10-1Translational Pharmacogenomics
  • Track 10-2Applications of NGS to Pharmacogenomics
  • Track 10-3Nutrigenomics
  • Track 10-4Toxicogenomics
  • Track 10-5Biomarker translation and testing
  • Track 10-6Cancer Pharmacogenomics
  • Track 10-7Pharmacogenitics & Individualized therapy
  • Track 10-8Pharmacogenomics in Clinical Therapeutics

Analytical and Bio analytical Techniques in which it includes analytical methods used for the characterization, release, and stability testing for chemical compounds and for new drugs also as well as the biotechnological/biological products and related to sciences and pharma.

  • Track 11-1Electro analytical methods
  • Track 11-2Spectroscopy
  • Track 11-3Gravimetric analysis
  • Track 11-4Electrophoresis
  • Track 11-5Ligand binding assays
  • Track 11-6Mass spectrometry
  • Track 11-7Nuclear magnetic resonance

Healthcare Management may be a totally different system within the management trade. In which it deals with the various field about leadership, management, administration of hospitals, hospital networks, etc. in Hospital Management it is a facility that the services are provided to the hospitals and patients.

  • Track 12-1Healthcare Planning and Marketing
  • Track 12-2Hospital Management and Big-Data Analytics
  • Track 12-3Hospital and Pharmaceutical management
  • Track 12-4Hospital Management and In/Out-patient Care
  • Track 12-5Hospital Management and Nursing
  • Track 12-6Medical Sociology and Public Health
  • Track 12-7Patient Safety
  • Track 12-8Public Health, Infection and Infectious Agents
  • Track 12-9Telemedicine and healthcare Administration

Industrial Pharmacy mainly deals with the drug research, design, development and also testing, treatments of new medicines, and more over ensuring safety and quality of drugs. And it includes areas relates to different functions in the pharmaceutical industry and having contact with the areas like engineering and economics.

  • Track 13-1Waste management
  • Track 13-2Product management
  • Track 13-3Post- marketing surveillance
  • Track 13-4Good manufacturing practices
  • Track 13-5Pharmaceutical Marketing
  • Track 13-6Pharmaceutical Marketing
  • Track 13-7Pharma Companies

Drug Regulatory Affairs refers to all aspects within the pharmaceutical development process and how they are subject to various degrees of regulation. The pharmaceutical law frame, guidelines covering Quality, Safety and Efficacy as well as Health Authorities' attitudes and requirements etc. have a great influence on the drug development process and the success of it. Regulatory affairs professionals deal with these aspects

  • Track 14-1Healthcare Regulatory Affairs
  • Track 14-2Pharmaceutical RA
  • Track 14-3Biologics and biotechnology RA
  • Track 14-4Medical devices RA
  • Track 14-5Biologics license application (BLA)

Industrial property (IP) rights are extremely important for the pharmaceutical industry. The use of the IP system by SMEs in the pharmaceutical industry depends largely on the business strategy of a company, its size, resources, innovative capacity, competitive context and field of expertise. Research-based, innovation-led companies that seek to develop new drugs improve or adapt existing drugs or develop new pharmaceutical/medical equipment or processes, tend to rely heavily on the patent system to ensure they recover the investments incurred in research and development

  • Track 15-1Trademarks
  • Track 15-2Trade dress
  • Track 15-3Infringement of rights
  • Track 15-4Copyright
  • Track 15-5Patents
  • Track 15-6Industrial design rights
  • Track 15-7Trade secrets