Call for Abstract

11th World Congress on Pharmaceutical Sciences, will be organized around the theme “An Insight in to Breakthroughs in Pharmacy & Pharmaceutical Sciences”

World Pharma Congress 2018 is comprised of 17 tracks and 100 sessions designed to offer comprehensive sessions that address current issues in World Pharma Congress 2018.

Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.

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

Pharmaceutical sciences combine a broad range of scientific disciplines that are involved with the design, action, delivery, disposition and use of drugs. This field draws on many areas of the basic and applied sciences such as chemistry, biology, epidemiology, statistics, chemometrics, mathematics, physics and chemical engineering and applies their principles to the study of drugs.


  • Track 1-1Pharmaceutical formulations
  • Track 1-2Biopharmaceutics
  • Track 1-3Preformulation studies
  • Track 1-4Pharmaceutical biotechnology
  • Track 1-5Routes of drug delivery
  • Track 1-6Pharmaceutical materials

Applied pharmaceutical science is a scientific discipline that applies existing scientific knowledge to develop more practical applications, such as technology or inventions. Applied pharmaceutical  science applies the basic science toward practical endeavors. Applied pharmaceutical science is typically engineering, which develops technology. Applied Pharmaceutical Sciences involve in either experimental or theoretical in the following areas:  Pharmaceutics & Biopharmaceutics, Novel &Targeted Drug Delivery, Nanotechnology& Nanomedicine, Pharmaceutical chemistry, Pharmacognosy & Ethnobotany Phytochemistry, Pharmacology & Toxicology, Pharmaceutical Biotechnology & Microbiology, Pharmacy practice & Hospital Pharmacy. 

  • Track 2-1Drug screening and discovery
  • Track 2-2Digital pharma
  • Track 2-3Biomaterials
  • Track 2-4Electrophoresis
  • Track 2-5Pharmacological testing
  • Track 2-6Drug therapies

Drug Discovery changes with the change in the dosage forms and the environmental conditions or   demand. It involves a wide range of scientific disciplines including biology, chemistry and pharmacology. Drug design involves the design of such molecules that are similar to the bio molecular target site in shape and charge in order to bind to it. The process of bringing a new pharmaceutical drug into the market once a lead compound has been identified through the process of drug discovery is called drug development and the research related to drug development is called drug development research.

  • Track 3-1Biomarkers in drug discovery
  • Track 3-2Ligand –based drug design
  • Track 3-3Computer – aided drug design
  • Track 3-4Genetics in drug development
  • Track 3-5Drug target
  • Track 3-6Rational drug design approach

The pharmaceutical industry includes the manufacture, extraction, processing, purification and packaging of chemical materials to be used as medications for humans or animals. Pharmaceutical manufacturing is divided into two major stages: the production of the active ingredient or drug (primary processing, or manufacture) and secondary processing .The pharmaceutical Manufacturing  is largely driven by scientific discovery and development, in conjunction with toxicological and clinical experience.

  • Track 4-1Pharmaceutical market
  • Track 4-2Medication management
  • Track 4-3Pharmaceutical industry
  • Track 4-4Introduction of modern engineering process
  • Track 4-5New measurement and control technologies
  • Track 4-6Development of lean validation and quality management

Pharmaceutical Development and Technology explores the research in the design, development, manufacture and evaluation of traditional and novel drug delivery systems- emphasizing practical solutions and applications to theoretical and research-based problems. Pharmaceutical products are made by transforming chemical compounds with useful effects on the human body into high-quality dosage forms that can appropriately exhibit effects against diseases. Efficacy and safety are the primary requirements for any pharmaceutical product. However, it is becoming significantly more important to provide pharmaceutical products that can be more easily used by patients, healthcare professionals and caregivers in order to respond to the rapid aging of society and the needs for advanced medical care.

  • Track 5-1Quality control
  • Track 5-2Pharmaceutical management
  • Track 5-3Drug delivery technologies
  • Track 5-4Medical devices
  • Track 5-5Pharmaceutical research
  • Track 5-6Pharmaceutical engineering

Radiopharmaceuticals are unique medicinal formulations containing radioisotopes which are used in major clinical areas for diagnosis or therapy, many radiopharmaceutical preparations contain radioisotopes with very short half-lives and such preparations therefore have very short shelf-lives and they require an expiry date and time to be indicated. Radiopharmaceutical preparation is a medicinal product in a ready-to-use form suitable for human use that contains a radionuclide. The radionuclide is integral to the medicinal application of the preparation, making it appropriate for one or more diagnostic or therapeutic applications

  • Track 6-1Clinical laboratory sciences
  • Track 6-2Radiopharmaceutical preparation
  • Track 6-3Radionuclide generator
  • Track 6-4Biomedical data engineering
  • Track 6-5Production of radioisotopes
  • Track 6-6Medicinal formulations

Nanotechnology is the science that deals with the processes that occur at molecular level and of nanolength scale size. Nanotechnology provides intelligent systems, devices and materials for better pharmaceutical applications. Pharmaceutical nanotechnology provides two basic types of nanotools, nanomaterials and nanodevices, which play a key role in realm of pharmaceutical nanotechnology and related fields. It is a combination of various fields like biophysics, bioengineering, and molecular biology and their combined disciplines. It has emerged successful in various medical fields.

  • Track 7-1Characterization of pharmaceutical nanotools and nanomaterials
  • Track 7-2Nano medicine
  • Track 7-3Biomedical nanotechnology
  • Track 7-4Nanoparticles and nanogels
  • Track 7-5Nano in pharmaceutical chemistry
  • Track 7-6Novel nanotechnology applications

Novel Drug Delivery System can be a major advance for solving the problems related towards the release of the drug at specific site with specific rate. The need for delivering drugs to patients efficiently and with fewer side effects has prompted pharmaceutical companies to engage in the development of new drug delivery system. The aim of novel drug delivery System is to provide a therapeutic amount of drug to the appropriate site in the body to accomplish promptly and then maintain the desired drug concentration.

  • Track 8-1Matrix diffusion types
  • Track 8-2Hydrogels
  • Track 8-3Targeted drug delivery
  • Track 8-4Drug loaded erythrocytes
  • Track 8-5Vaccine drug delivery system
  • Track 8-6Advanced drug delivery

Bioavailability means the rate and extent to which the active drug substance or therapeutic moiety is absorbed from a pharmaceutical form and becomes available at the site of action. For drugs intended to exhibit a systemic therapeutic effect, bioavailability can be more simply understood as the rate and extent to which a substance or its therapeutic moiety is delivered from a pharmaceutical form into the general circulation. Bioequivalence focus on the release of a drug substance from a drug product and subsequent absorption into systemic circulation. Bioequivalence studies are a surrogate marker for clinical effectiveness and safety data as it would not normally be practical to repeat clinical studies for generic products.


  • Track 9-1Invitro bioequivalence
  • Track 9-2Bioequivalence study design
  • Track 9-3Genetic phenotyping
  • Track 9-4Bioequivalence study protocols
  • Track 9-5Waiver of invivo bioavailability
  • Track 9-6Bioavailability metrics

Clinical research as a component of medical and health research intended to produce valuable knowledge for understanding of human disease, preventing and treating illness and promoting health. Clinical research involves interactions with patients, diagnostic clinical materials or data or populations. Clinical research and its translation into preventive and clinical care. Clinical trials are research investigations in which people volunteer to test new treatments, interventions or tests as a means to prevent, detect, treat or manage various diseases or medical conditions. Clinical trials can also help to improve health care services by raising standards of treatment.

  • Track 10-1Clinical data management and statistics
  • Track 10-2Clinical research methods
  • Track 10-3Clinical pharmacy and pharmacy community
  • Track 10-4Clinical case report
  • Track 10-5Design of clinical studies and trails
  • Track 10-6Medicinal research

Pharmaceutical analytical techniques deal with the different processes to identify or quantify a substance. The components of a pharmaceutical solution or mixture or the determination of the structures of chemical compounds used in the formulation of pharmaceutical product. These pharmaceuticals may develop impurities at various stages of their development, transportation and storage which makes the pharmaceutical risky to be administered thus they must be detected and quantified. For this analytical instrumentation and methods play an important role. Variety of analytical techniques such as titrimetric, chromatographic, spectroscopic, electrophoretic and electrochemical and their corresponding methods that have been applied in the analysis of pharmaceuticals.

  • Track 11-1Forensic analytical techniques
  • Track 11-2Analytical methodology
  • Track 11-3Electro analytical methods
  • Track 11-4Applications of analytical and bioanalytical methods
  • Track 11-5HPLC analytical method development and validation
  • Track 11-6Biomarker validation

The World Health Organization (WHO) defines pharmacovigilance as the science and activities relating to the detection, evaluation, understanding and prevention of adverse reactions to medicines or any other medicine-related problems. Pharmacovigilance is to protect patients and the public wherever possible and to disseminate knowledge among the relevant professional communities and to patients in order to minimise risk. Pharmacovigilance system or the processes to be engaged in risk management, there is consensus among the major regulators that pharmacovigilance is necessary and important in the development and commercialization of medicinal products.

  • Track 12-1Pharmacovigilance practice
  • Track 12-2Information technology in pharmacovigilance
  • Track 12-3Pharmacy practice and it’s challenges
  • Track 12-4Implementation of risk minimization
  • Track 12-5Pharmacovigilance significance and scope
  • Track 12-6Drug safety

 GMP ensures that quality is built into the organization and processes involved in the manufacture of the products and all those operations should be carried out strictly according to cGMP. Current Good Manufacturing Practices, formal regulations contained in statutes and agency policies and concern the design, monitoring and control of manufacturing processes and facilities. GCP (Good Clinical Practice) is an international ethical and scientific quality standard for the performance of a clinical trial on medicinal products involving humans. GCP includes all aspects of a clinical trials. Regulatory affairs is a comparatively new profession which developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines

  • Track 13-1Sterile pharmaceutical or biological medicinal products
  • Track 13-2GMP regulations
  • Track 13-3Clinical investigation of medical devices
  • Track 13-4Clinical safety data management
  • Track 13-5Health care regulatory affairs
  • Track 13-6Regulatory requirement of pharmaceutical products

Pharmaceutical Packaging can be defined as an economical means of providing presentation, protection, identification information, containment, convenience and compliance for a product during storage, carriage, display and until the product is consumed. Packaging must provide protection against climatic conditions biological, physical and chemical hazards and must be economical. Pharmaceutical marketing is based on product type and geography. The pharmaceutical packaging market is constantly advancing and has experienced annual growth of at least five percent per annum in the past few years as with most other packaged goods, pharmaceuticals need reliable and speedy packaging solutions that deliver a combination of product protection, quality, tamper evidence, patient comfort and security needs.

  • Track 14-1Properties of packing material
  • Track 14-2Pharmacoeconomics
  • Track 14-3Shrink seal and bands
  • Track 14-4Medico marketing
  • Track 14-5Blister packages
  • Track 14-6Strip packages

A drug interaction is a situation in which a substance (usually another drug) affects the activity of a drug when both are administered together. This action can be synergistic (when the drug's effect is increased) or antagonistic (when the drug's effect is decreased) or a new effect can be produced that neither produces on its own. Typically, interactions between drugs come to mind (drug-drug interaction). However, interactions may also exist between drugs and foods (drug-food interactions), as well as drugs and medicinal plants or herbs (drug-plant interactions). People taking antidepressant drugs such as monoamine oxidase inhibitors should not take food containing tyramine as hypertensive crisis may occur (an example of a drug-food interaction). These interactions may occur out of accidental misuse or due to lack of knowledge about the active ingredients involved in the relevant substances.

  • Track 15-1Global pharmaceutical market
  • Track 15-2Technological innovations
  • Track 15-3R&D management
  • Track 15-4Emerging markets
  • Track 15-5Innovations of drug enhancements
  • Track 15-6Public –Private partnership

Hospital pharmacy is a specialized field of pharmacy that is integrated into the care of a medical center. These include centers such as a hospital, outpatient clinic, drug-dependency facility, poison control center, drug information center of residential care facility. Industrial Pharmacy is a discipline which includes manufacturing, development, marketing and distribution of drug products including quality assurance of these activities. The pharmaceutical industry is an important component of health care systems throughout the world.

  • Track 16-1Drug information center
  • Track 16-2Health care system
  • Track 16-3Pharmaceutical research and development
  • Track 16-4Medical and pharmacy affairs
  • Track 16-5Distribution of drug product
  • Track 16-6Production of quality goods