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World Congress on Advanced Pharmacy and Industrial Research, will be organized around the theme “Advanced Research Approaches & Scientific Innovations in Industrial Pharmacy”

Advanced Pharmacy 2018 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Advanced Pharmacy 2018

Submit your abstract to any of the mentioned tracks.

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The scope of  Advanced pharmacy practice includes more traditional roles such as compounding and dispensing medications, and it also includes more modern services related to health care, including clinical services, reviewing medications for safety and efficacy, and providing drug information. Pharmacists, therefore, are the experts on Remedial treatment and are the primary health professionals who optimize use of medication for the benefit of the patients.

An establishment in which pharmacy (in the first sense) is practiced is called a pharmacy (this term is more common in the United States) or a Analyst (which is more common in Great Britain). In the United States and Canada, drugstores commonly sell medicines, as well as miscellaneous items such as confectionery, cosmetics, office supplies, toys, hair care products and magazines and occasionally refreshments and groceries.

  • Track 1-1Foundations in Primary Care Practice
  • Track 1-2Advanced Therapeutics
  • Track 1-3Medication Management, Safety and Quality
  • Track 1-4Care Transitions
  • Track 1-5Medication Adherence
  • Track 1-6Medication Therapy Management

Formulation studies then consider such factors as particle size, multifariousness, pH, and solubility, as all of these can influence bioavailability and hence the activity of a drug. The drug must be combined with Stable ingredients by a method which ensures that the Assessment of drug present is consistent in each dosage unit e.g. each tablet. The dosage should have equal appearance, with an acceptable taste, tablet hardness, or capsule disintegration.

It is unlikely that formulation studies will be complete by the time scientific trials commence. This means that simple preparations are developed initially for use in phase I scientific trials. These typically consist of hand-filled capsules containing a small amount of the drug and a diluent. Proof of the long-term stability of these production is not required, as they will be used (tested) in a matter of days. Consideration has to be given to what is known as "drug loading" - the ratio of the active drug to the total contents of the dose. A low drug load may cause uniform problems. A high drug load may pose flow problems or require large capsules if the compound has a low bulk density.

  • Track 2-1Types of formulation
  • Track 2-2Bioavailability of Drugs
  • Track 2-3Pre-formulation &Formulation aspects
  • Track 2-4Research Advancements in Drug Formulation
  • Track 2-5ADME Compliances

Drug design, often referred to as rational drug design or simply rational design, is the innovative 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 reciprocal in shape and charge to the bio-molecular target with which they interact and therefore will bind to it. Drug design regularly but not necessarily relies on computer modeling techniques. This type of modeling is sometimes referred to as computer-aided drug design. 

  • Track 3-1Biomarkers in medical science
  • Track 3-2Bioinformatics in CADD
  • Track 3-3Ligand based CADD
  • Track 3-4Steps Involved in CADD
  • Track 3-5Pharmacophore Therapy

The phrase "drug design" is to some extent a misnomer. A more accurate term is ligand design (i.e., design of a molecule that will bind tightly to its target). Although design techniques for envision of binding affinity are reasonably successful, there are many other properties, such as bioavailability, metabolic half-life, side effects, etc., that first must be optimized before a ligand can become a safe and effective  drug. These other characteristics are often difficult to predict with rational design techniques. Still, due to high attrition rates, especially during clinical phases of drug development, more attention is being focused early in the drug design process on selecting candidate drugs whose physicochemical properties are anticipated to result in fewer complications during development and hence more likely to lead to an approved, marketed drug. Moreover, in vitro experiments complemented with computation methods are increasingly used in early drug discovery to select compounds with more favorable ADME (absorption, distribution, metabolism, and excretion) and toxicological profiles.

  • Track 4-1Receptor-based Drug Design
  • Track 4-2Pharmacophore based Drug Design
  • Track 4-3Structural based drug designing
  • Track 4-4Procedure for Drug Designing
  • Track 4-5Drug Designing Docking&Rational Drug Design
  • Track 4-6Combination Therapy
  • Track 4-7Pharmacophore Therapy

Drug delivery technologies modify drug release profile, absorption, distribution and elimination for the advantage of improving product efficacy and safety, as well as patient convenience and compliance. Drug release is from diffusion, disintegration, degradation, swelling, and affinity-based mechanisms. Most common routes of administration include the favored non-invasive perioral (through the mouth), topical (skin), trans-mucosal (nasal, buccal /sublingual, vaginal, ocular and rectal) and inhalation routes. Many medications such as peptide and protein, antibody, vaccine and gene based drugs, in general may not be delivered using these routes because they might be impressionable to enzymatic reduction or cannot be absorbed into the systemic circulation regularly due to molecular size and charge issues to be therapeutically effective. For this reason many protein and peptide drugs have to be delivered by injection or a nano needle array. 

  • Track 5-1Nano Drug Delivery Systems
  • Track 5-2Polymeric Drug Delivery Systems
  • Track 5-3Drug Metabolites Novel Drug Delivery System
  • Track 5-4Transdermal Drug Delivery System
  • Track 5-5Protein-Protein Interactions as Drug Targets
  • Track 5-6Advances in Drug Delivery

Analytical chemistry studies and uses instruments and design used to separate, identify, and quantify matter. In practice separation, recognition or quantification may constitute the entire analysis or be combined with another method. Separation isolates analytes. Qualitative analysis recognizes analytes, while quantitative analysis determines the numerical amount or concentration.

Analytical chemistry consists of academic, wet chemical methods and technical, instrumental methods. Classical qualitative methods use separations such as precipitation, extraction, and distillation. Recognition may be based on differences in gloss, odour, melting point, boiling point, radioactivity or reactivity. Academic quantitative analysis uses mass or volume changes to asses the amount. Instrumental methods may be used to separate samples using chromatography, electrophoresis or field flow fractionation. Then qualitative and quantitative analysis can be implemented, often with the same instrument and may use light interaction, heat interaction, electric fields or magnetic fields . Often the same instrument can separate, identify and evaluate an analyte.

  • Track 6-1Chromatographic Techniques for Drug Analysis
  • Track 6-2Gravimetric Analysis
  • Track 6-3Electrophoresis
  • Track 6-4Method Development and Evaluation studies

A drug interaction is a situation in which a substance (usually another drug) affects the action 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. Mostly these are of different types of drug interaction studies. 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 like 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 7-1Types of Drug interaction studies
  • Track 7-2In-vitro & In-vivo Studies
  • Track 7-3Drug Toxicity
  • Track 7-4Etymology
  • Track 7-5Advances in Chromatographic Studies

Regulatory Affairs is a profession within regulated industries namely-pharmaceuticals, Medicinal devices, energy and banking. It has specific meaning within healthcare industries namely- pharmaceuticals, therapeutic devices, biologics and functional foods. Regulatory Affairs in the pharma industry may be defined as "The interface between the pharmaceutical company and the regulatory agencies across the world." Regulatory agency in the present context may be defined as "The competent government agency which is responsible for ensuring that medicines work and are acceptably safe."

  • Track 8-1Regulatory Communications and Submissions
  • Track 8-2Intellectual Property Rights
  • Track 8-3Regulatory Requirements for Pharmaceuticals
  • Track 8-4Regulatory Strategies and Developments
  • Track 8-5Global Regulatory Intelligence
  • Track 8-6Priorities Of International Agenda
  • Track 8-7Code of Federal Regulations
  • Track 8-8Clinical Affairs & Regulatory Strategies

Chromatography is a laboratory technique for the separation of a two or more compounds. The mixture is dissolved in a solvent called the mobile phase, which carries it through a structure holding another material called the stationary phase. The various components 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 affect the separation. Mostly there are different types of Chromatographic new techniques available like Hyphenated technique, super critical fluid chromatography, HPLC, TLC, etc.

  • Track 9-1Novel &Electro migrationTechniques in Chromatography
  • Track 9-2High Performance Liquid Chromatography
  • Track 9-3Multidimensional Chromatography
  • Track 9-4Applications of Chromatography
  • Track 9-5Market Analysis for Chromatographic Studies

Pharmacovigilance also known as drug  safety, is the pharmacological science combines the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. Pharmacovigilance and its Significance and Scope present the case for the importance of pharmacovigilance, to record its growth and potential as an important discipline within Medicinal science, and to describe its impact on patient health and public health and to know what is pharmacovigilance. In this track, we discussed about the Significance of pharmacovigilance. We also discussed on Pharmacovigilance role in healthcare system. Worldwide every year so many pharmacovigilance conferences were going on.

  • Track 10-1Genetic Drug Submissions
  • Track 10-2NDA & ANDA Filling
  • Track 10-3Approved and non-approved Drugs for Pharmacovigilance
  • Track 10-4Food Drug & Cosmetic laws
  • Track 10-5FDA and related regulatory agencies
  • Track 10-6Good Pharmacovigilance Practices

Drug discovery is the process through which potential new medicines are identified and comprises an extensive range of scientific disciplines, including morphology, chemistry and pharmacology. The integration of pharmacodynamics and pharmacokinetic parameters in non-clinical pharmacology studies is a key role in drug discovery for potent and safety assessment, in the particular for the translation from the non-clinical to  clinical field and process of drug discovery include  the recognition of candidates, synthesis, characterization, screening, and assays for therapeutic efficacy where as modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to raising the affinity, selectivity, efficacy/potency, metabolic stability, and oral bioavailability. The "final product" of drug discovery is a patent on the potential drug.

  • Track 11-1Innovations in Drug design
  • Track 11-2Preclinical trials for Drug Development
  • Track 11-3Analysis for Drug development
  • Track 11-4SAR for Drug development
  • Track 11-5Advanced technology in Drug discovery

Pharmacology is the branch of biology deals 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 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 relation 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 12-1Development Techniques in Drug Screening
  • Track 12-2Different types of toxicological Studies
  • Track 12-3Research innovations in Pharmacological studies
  • Track 12-4Pharmacokinetics & Pharmacodynamics for Pharmacology
  • Track 12-5Nursing & Neuropharmacology
  • Track 12-6Pharmacological testing

The branch of Science explained with medicinal drugs obtained from plants or other natural sources Pharmacognosy is in the strict feeling of the word came after investigation of phytochemicals. A significant number of these are known not security against germ assaults and plant ailments. They additionally show various preventive capacities for human purchasers. Phytochemistry can be considered sub-fields of Biology or Chemistry. Exercises can be driven in natural greenery enclosures or in the wild with the guide of Ethnobotany. The uses of the order can be for Pharmacognosy, or the disclosure of new medications or as a guide for plant physiology contemplates. Phytochemical procedure mostly applies to the quality control of Chinese solution, medicinal plants (Indian conventional drug) or home grown prescription of different combination segments, for example, saponins, alkaloids, unpredictable oils, flavonoids and glycosides.

  • Track 13-1Techniques for Plant extraction
  • Track 13-2Advancement in Tissue Culture
  • Track 13-3Plant Phytopharmaceuticals
  • Track 13-4Molecular Techniques in industrial Pharmacogonosy
  • Track 13-5Crude drug extraction
  • Track 13-6Economy for Herbal & Cosmetics

Analytical chemistry studies and uses instruments and methods used to separate, recognise, calibrate and quantify matter. In practice separation, identification or quantification may constitute the entire analysis or be combined with another method. Separation isolates analytes. Qualitative analysis identifies analytes, while quantitative analysis determines the differential amount or concentration.Pharmaceutical marketing, sometimes called medico-marketing or biological  marketing in some countries, is the business of advertising or otherwise promoting the sale of pharmaceutical drugs. Many countries have measures in place to limit advertising by pharmaceutical companies.

  • Track 14-1Market Analysis for Pharmaceutical products
  • Track 14-2QC & QA studies
  • Track 14-3Drug Evaluation Methods for Pharmaceuticals
  • Track 14-4Development Trends & Strategies on Analysis
  • Track 14-5ICH guidelines for Pharmaceuticals
  • Track 14-6Advanced techniques for validation

Good manufacturing practices (GMP) are the practices required in order to conform to the guidelines recommended by agencies that control authorization and grant for manufacture and sale of food, drug products, and active pharmaceutical products. These guidelines provide minimum requirements that a pharmaceutical or a food product manufacturer must meet to assure that the products are of high quality and do not pose any risk to the consumer or public. Good manufacturing practices, along with good agricultural practices, good laboratory practices and good pharmacy practices, are overseen by administrative agencies in the United States, Canada, Europe, China, and other countries.

  • Track 15-1GMP & GLP Guidelines
  • Track 15-2Latest Advances in Pharmacy Practice
  • Track 15-3Role of a pharmacist in Pharmacy practice
  • Track 15-4Scope & Significance in pharmaceutical Field
  • Track 15-5Marketing For Pharmacy Practice

Pharmaceutical drug delivery technologies improve drug absorption, efficacy, and patient experience. Taste maskers raising the commercial activity of your pharmaceutical products by neutralizing the strong, bitter tastes of certain oral medical formulations. Bioavailability of medications within the system can be achieved by increasing the dissolution rate with specialized drug delivery improvement products. Enhancing the drug delivery technology of final pharmaceutical formulation can raising its commercial success. The main routes of drug delivery are oral, injection/infusion, and transdermal. Drug-eluting stents and other implantable drug delivery devices are presented, as well as apparently applied devices. When combined with appropriate targeting molecules, drug-coated nanoparticles, drug-encapsulating liposomes and nanosomes, and tree-like dendrimers enable organ and tissue targeting.

  • Track 16-12D & 3D in drug delivery
  • Track 16-2Factors influencing the Novel Drug Delivery System
  • Track 16-3Role of Computers in Drug Design therapy
  • Track 16-4Methods & Advanced techniques in Novel Drug Delivery system
  • Track 16-5Recent Approaches & Advances in Drug Targeting
  • Track 16-6Future Prospects for Pharmaceutical Nanotechnology
  • Track 16-7Advances in self-emulsifying drug delivery system

Industrial pharmacy is a disciplinary subject which includes manufacturing, development, marketing and distribution of drug products including cross checking of these activities. The research topics are focused on solving current general problems in pharmaceutical industry, such as formulation and characterization of sticky amorphous drugs, problem-solving for pediatric medicines and miniaturization of manufacturing processes. Physical pharmacy incorporates information of arithmetic, material science and science and applies them to the pharmaceutical dose frame enhancement. Physical pharmacy gives the premise to understanding the synthetic and physical wonders that oversee the in vivo and in vitro activities of pharmaceutical items.

  • Track 17-1Scope & Importance for Industrial Pharmacy
  • Track 17-2De-Novo Advancement in industrial Pharmacy
  • Track 17-3Regulatory & Patient Compliance in Physical Pharmacy
  • Track 17-4Significance for Physical Pharmacy
  • Track 17-5Innovations & Advance Techniques in Industrial & Physical Pharmacy
  • Track 17-6Post- Marketing Surveillance
  • Track 17-7Development Methods for Physical Pharmacy Practice