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16th Annual Medicinal & Pharmaceutical Sciences Congress, will be organized around the theme “Developing the Synergy between Pharmaceutics and Medicinal Chemistry to Deliver Better Drugs”

Med Pharma Congress 2017 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 2017

Submit your abstract to any of the mentioned tracks.

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

The Pharmaceutical Sciences are a group of interdisciplinary areas of study concerned with the design, action, delivery and disposition of drugs. They apply knowledge from Chemistry (inorganic, physical, biochemical and analytical), biology (anatomy, physiology, biochemistry, cell biology and molecular), epidemiology, statistics, chemo metrics, mathematics, physics, and chemical engineering.

  • Track 1-1Drug Screening and Discovery
  • Track 1-2Pharmacological Testing
  • Track 1-3Advances in Pharmaceutical Research
  • Track 1-4R&D Advancement
  • Track 1-5Principles of Good Manufacturing Practice
  • Track 1-6Digital Pharma

Medicinal chemistry and pharmaceutical chemistry are disciplines at the intersection of chemistry, especially synthetic organic chemistry, and pharmacology and various other biological specialties, where they are involved with design, chemical synthesis and development for market of pharmaceutical agents, or bio-active molecules (drugs). Compounds used as medicines are most often organic compounds, which are often divided into the broad classes of small organic molecules (e.g., atorvastatin, fluticasone, clopidogrel) and "biologics" (infliximab, erythropoietin, insulin glargine), the latter of which are most often medicinal preparations of proteins (natural and recombinant antibodies, hormones, etc.). Inorganic and organometallic compounds are also useful as drugs (e.g., lithium and platinum-based agents such as lithium carbonate and cis-platin as well as gallium).

  • Track 2-1Identification and validation of drug targets
  • Track 2-2Structural biology
  • Track 2-3Drug ability of targets
  • Track 2-4Drug design approaches
  • Track 2-5Synthetic chemistry including combinatorial methods
  • Track 2-6Bioorganic chemistry

Pharmacology is the branch of medicine and biology concerned with the study of drug action, where a drug can be broadly defined as any man-made, natural, or endogenous (from within body) molecule which exerts a biochemical and/or physiological effect on the cell, tissue, organ, or organism (sometimes the word pharmacon is used as a term to encompass these endogenous and exogenous bioactive species). More specifically, it is the study of the interactions that occur between a living organism and chemicals that affect normal or abnormal biochemical function. If substances have medicinal properties, they are considered pharmaceuticals.

  • Track 3-1Cardiovascular Pharmacology
  • Track 3-2Clinical pharmacology
  • Track 3-3Neuropharmacology
  • Track 3-4Psychopharmacology
  • Track 3-5Systems Pharmacology
  • Track 3-6Theoretical pharmacology
  • Track 3-7Behavioral pharmacology
  • Track 3-8Environmental pharmacology
  • Track 3-9Ocular Pharmacology
  • Track 3-10Biochemical Pharmacology
  • Track 3-11Continental Pharmacovigilance
  • Track 3-12Good Pharmacovigilance Practice
  • Track 3-13Pharmacovigilance and Risk Management

Chromatography from Greek Chroma which means "color" and graphing "to write" is the collective term for a set of laboratory techniques for the separation of mixtures. The mixture is dissolved in a fluid called the mobile phase, which carries it through a structure holding another material called the stationary phase. The various constituents of the mixture travel at different speeds, causing them to separate. The separation is based on differential partitioning between the mobile and stationary phases. Subtle differences in a compound's partition coefficient result in differential retention on the stationary phase and thus changing the separation.

  • Track 4-1Flash column chromatography
  • Track 4-2Paper chromatography
  • Track 4-3Thin layer chromatography
  • Track 4-4Displacement chromatography
  • Track 4-5Hydrophobic interaction chromatography
  • Track 4-6Reversed-phase chromatography
  • Track 4-7Expanded bed adsorption chromatographic separation
  • Track 4-8Chiral chromatography

Synthetic organic chemistry is an applied science as it borders engineering, the "design, analysis, and/or construction of works for practical purposes". Organic synthesis of a novel compound is a problem solving task, where a synthesis is designed for a target molecule by selecting optimal reactions from optimal starting materials. Complex compounds can have tens of reaction steps that sequentially build the desired molecule. The synthesis proceeds by utilizing the reactivity of the functional groups in the molecule. For example, a carbonyl compound can be used as a nucleophile by converting it into an enolate, or as an electrophile; the combination of the two is called the aldol reaction. Designing practically useful syntheses always requires conducting the actual synthesis in the laboratory. The scientific practice of creating novel synthetic routes for complex molecules is called total synthesis.

  • Track 5-1Stereo controlled synthesis of complex organic molecules
  • Track 5-2Organic synthesis and combinatorial chemistry
  • Track 5-3Chemical methodologies, natural product synthesis, and chemical genomics
  • Track 5-4Organic synthesis and natural products

A biopharmaceutical, also known as a biological medical product, biological, or biologic, is any pharmaceutical drug product manufactured in, extracted from, or semi synthesized from biological sources. Different from totally synthesized pharmaceuticals, they include vaccines, blood, blood components, allergenic, somatic cells, gene therapies, tissues, recombinant therapeutic protein, and living cells used in cell therapy. Biologics can be composed of sugars, proteins, or nucleic acids or complex combinations of these substances, or may be living cells or tissues. They (or their precursors or components) are isolated from living sources—human, animal, plant, fungal, or microbial.

  • Track 6-1Pharmacokinetics and Pharmacodynamics
  • Track 6-2Bioavailability and bioequivalence
  • Track 6-3Bio waiver
  • Track 6-4Biological Medicine
  • Track 6-5Novel Approaches in Bio Pharmaceutics
  • Track 6-6Invivo-invitro correlation

Pharmacogenomics is the study of the role of the genome in drug response. Its name reflects its combining of pharmacology and genomics. Pharmacogenomics can be defined as the technology that analyzes how the genetic makeup of an individual affects his/her response to drugs. It deals with the influence of acquired and inherited genetic variation on drug response in patients by correlating gene expression or single-nucleotide polymorphisms with pharmacokinetics and pharmacodynamics (drug absorption, distribution, metabolism, and elimination), as well as drug receptor target effects. The term pharmacogenomics is often used interchangeably with pharmacogenetics. Although both terms relate to drug response based on genetic influences, pharmacogenetics focuses on single drug-gene interactions, while pharmacogenomics encompasses a more genome-wide association approach, incorporating genomics and epigenetics while dealing with the effects of multiple genes on drug response.

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

Pharmacognosy is the study of medicinal drugs derived from plants or other natural sources. The American Society of Pharmacognosy defines pharmacognosy as "the study of the physical, chemical, biochemical and biological properties of drugs, drug substances or potential drugs or drug substances of natural origin as well as the search for new drugs from natural sources. It is also defined as the study of crude drugs. Phytochemistry is the study of phytochemicals, which are chemicals derived from plants. Specifically, phytochemistry describes the large number of secondary metabolic compounds found in plants. Many of these are known to provide protection against insect attacks and plant diseases. They also exhibit a number of protective functions for human consumers.  Phytochemistry can be considered sub-fields of botany or chemistry. Activities can be led in botanical gardens or in the wild with the aid of ethnobotany. The applications of the discipline can be for pharmacognosy, or the discovery of new drugs, or as an aid for plant physiology studies

  • Track 8-1Drugs from natural sources
  • Track 8-2Molecular drug design
  • Track 8-3Structure aided and computer aided drug design
  • Track 8-4Telemedicine

Pharmaceutical Toxicology explains the methodology and requirements of pre-clinical safety assessments of new medicines. With the focus on medicinal drugs, the most important safety issues of drugs are covered. This includes registration requirements of new drugs and pharmacovigilance.

  • Track 9-1Regulatory toxicology
  • Track 9-2Analytical toxicology
  • Track 9-3Plant toxicology
  • Track 9-4Toxicologic Pathology
  • Track 9-5Biodegradation
  • Track 9-6Toxicokinetics

Industrial Pharmacy also plays a crucial role in any drug discovery. To any novel drug discovery the industrial approach is very important to get massive commercial application. Few things which have to be considered by industries to provide a safe and cost affective medicine to the patients like Supply chain, Waste management, Product management, Post- marketing surveillance, Good manufacturing practices and Marketing.

  • Track 10-1Waste management
  • Track 10-2Product management
  • Track 10-3Post- marketing surveillance
  • Track 10-4Good manufacturing practices
  • Track 10-5Pharmaceutical Marketing
  • Track 10-6Pharma Companies
  • Track 10-7Pharma Manufacturing

Regulatory affairs (RA), is also called government affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, banking, telecom etc. Regulatory affairs also has a very specific meaning within the healthcare industries (pharmaceuticals, medical devices, biologics and functional foods)

  • Track 11-1Healthcare Regulatory Affairs
  • Track 11-2Pharmaceutical RA
  • Track 11-3Biologics and Biotechnology RA
  • Track 11-4Medical devices RA

Pharmaceutical formulation, in pharmaceutics, is the process in which different chemical substances, including the active drug, are combined to produce a final medicinal product. The word formulation is often used in a way that includes dosage form. 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 12-1Oral drugs
  • Track 12-2Parental Formulations
  • Track 12-3Topical Formulations
  • Track 12-4Modified release Formulations
  • Track 12-5Novel Drug Formulations
  • Track 12-6Oncological Formulations
  • Track 12-7Cosmetics
  • Track 12-8Cosmetics
  • Track 12-9Veterinary Products

Computational chemistry is a branch of chemistry that uses computer simulation to assist in solving chemical problems. It uses methods of theoretical chemistry, incorporated into efficient computer programs, to calculate the structures and properties of molecules and solids. It is necessary because, apart from relatively recent results concerning the hydrogen molecular ion (dihydrogen cation, see references therein for more details), the quantum many-body problem cannot be solved analytically, much less in closed form. While computational results normally complement the information obtained by chemical experiments, it can in some cases predict hitherto unobserved chemical phenomena. It is widely used in the design of new drugs and materials. Examples of such properties are structure (i.e., the expected positions of the constituent atoms), absolute and relative (interaction) energies, electronic charge density distributions, dipoles and higher multipole moments, vibrational frequencies, reactivity, or other spectroscopic quantities, and cross sections for collision with other particles.

  • Track 13-1Ab initio methods
  • Track 13-2Density functional methods
  • Track 13-3Semi-empirical and empirical methods
  • Track 13-4Molecular mechanics
  • Track 13-5Chemical dynamics
  • Track 13-6Molecular dynamics

Nano medicine is the medical application of nanotechnology. Nano medicine ranges from the medical applications of nanomaterial’s and biological devices, to Nano electronic biosensors, and even possible future applications of molecular nanotechnology such as biological machines. Current problems for Nano medicine involve understanding the issues related to toxicity and environmental impact of Nano scale materials (materials whose structure is on the scale of nanometers, i.e. billionths of a meter). Functionalities can be added to nanomaterial by interfacing them with biological molecules or structures. The size of nanomaterial’ is similar to that of most biological molecules and structures; therefore, nanomaterial’s can be useful for both in vivo and in vitro biomedical research and applications. Thus far, the integration of nanomaterial with biology has led to the development of diagnostic devices, contrast agents, analytical tools, physical therapy applications, and drug delivery vehicles.

  • Track 14-1Nano Materials
  • Track 14-2Biological Devices
  • Track 14-3Nano electronic Biosensors
  • Track 14-4Nano Scale Materials

An analytical technique is a method that is used to determine the concentration of a chemical compound or chemical element. There are a wide variety of techniques used for analysis, from simple weighing (gravimetric analysis) to titrations (titrimetric) to very advanced techniques using highly specialized instrumentation. Bioanalysis is a sub-discipline of analytical chemistry covering the quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotics (macromolecules, proteins, DNA, large molecule drugs, metabolites) in biological systems.

  • Track 15-1Electro Analytical Methods
  • Track 15-2Spectroscopy
  • Track 15-3Electrophoresis
  • Track 15-4Gravimetric analysis
  • Track 15-5Ligand binding assays
  • Track 15-6Mass spectrometry
  • Track 15-7Nuclear Magnetic Resonance

Drug design, often referred to as rational drug design or simply rational design, is the inventive process of finding new medications based on the knowledge of a biological target. The drug is most commonly an organic small molecule that activates or inhibits the function of a biomolecule such as a protein, which in turn results in a therapeutic benefit to the patient. In the most basic sense, drug design involves the design of molecules that are complementary in shape and charge to the biomolecular target with which they interact and therefore will bind to it. Drug design frequently but not necessarily relies on computer modeling techniques. This type of modeling is sometimes referred to as computer-aided drug design. Finally, drug design that relies on the knowledge of the three-dimensional structure of the biomolecular target is known as structure-based drug design. In addition to small molecules, biopharmaceuticals and especially therapeutic antibodies are an increasingly important class of drugs and computational methods for improving the affinity, selectivity, and stability of these protein-based therapeutics have also been developed.

  • Track 16-1Rational Drug Design
  • Track 16-2Computer-aided drug design
  • Track 16-3Structure-based drug design
  • Track 16-4Dosage form
  • Track 16-5Route of administration

Clinical pharmacy is the branch of pharmacy in which pharmacists provide patient care that optimizes the use of medication and promotes health, wellness, and disease prevention. Clinical pharmacists care for patients in all health care settings but the clinical pharmacy movement initially began inside hospitals and clinics. Clinical pharmacists often work in collaboration with physicians, nurse practitioners, and other healthcare professionals.

  • Track 17-1Clinical Pharmacy and Therapeutics
  • Track 17-2Pre-Clinical and Clinical Trials
  • Track 17-3Clinical Trials on Various Disorders
  • Track 17-4Clinical Research and Statistics
  • Track 17-5Clinical Pharmacy Activities and Prescriptions
  • Track 17-6Clinical Pharmacy and Drug Reactions
  • Track 17-7Dispensing Pharmacy and Research Chemists

Intellectual property (IP) refers to creations of the intellect for which a monopoly is assigned to designated owners by law. Intellectual property rights (IPRs) are the protections granted to the creators of IP, and include trademarks, copyright, patents, industrial design rights, and in some jurisdictions trade secrets. Artistic works including music and literature, as well as discoveries, inventions, words, phrases, symbols, and designs can all be protected as intellectual property.

  • Track 18-1Patents
  • Track 18-2Copyright
  • Track 18-3Industrial Design Rights
  • Track 18-4Plant varieties
  • Track 18-5Trademarks
  • Track 18-6Trade dress
  • Track 18-7Trade secrets