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European Congress on Pharmaceutical Science and Technology , will be organized around the theme “Exploring the recent research and Innovations in Pharma Industry”

Euro Pharma 2019 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Euro Pharma 2019

Submit your abstract to any of the mentioned tracks.

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

Pharmaceutical formulation is the process in which different chemical substances, like the active drug, are combined to produce a final medicinal product. Formulation word is often used in a way that it includes dosage form.

Formulation studies include developing a preparation of the drug which is stable as well as acceptable to the patient. For orally administered drugs, this mostly involves incorporating the drug into a tablet or a capsule form.

Formulation studies then consider factors such as particle size, polymorphism, pH, and solubility, as all of these can influence the activity of a drug affected by change in bioavailability. The drug should be combined with inactive ingredients by a method which ensures that the quantity of drug used is consistent in each dosage unit e.g. each capsule or tablet. The dosage should have a uniform appearance, tablet hardness, capsule disintegration and with an acceptable taste.

 

  • Track 1-1Pre formulation
  • Track 1-2Nanoparticles
  • Track 1-3Encapsulation
  • Track 1-4Oral drugs
  • Track 1-5Parental Formulations
  • Track 1-6Topical Formulations
  • Track 1-7Modified release Formulations
  • Track 1-8Novel Drug Formulations
  • Track 1-9Serious Adverse Events
  • Track 1-10Biological medicines

Drug manufacturing is the process of synthesis of pharmaceutical drugs at industrial-scale by pharmaceutical companies. The process of drug manufacturing can be categorised into a number of unit operations, such as milling, granulation, coating, tablet pressing, and others.

 

 

  • Track 2-1Powder blending
  • Track 2-2Milling
  • Track 2-3Granulation
  • Track 2-4Hot melt extrusion
  • Track 2-5 Coating
  • Track 2-6Tablet pressing

Pharmacokinetics is a branch of pharmacology dedicated to determining the fate of substances administered to a living organism. The substances of interest include any chemical xenobiotic such as: pharmaceutical drugs, food additives, cosmetics, pesticides etc.

Pharmacokinetics shows the effects of body to a specific chemical after administration through the mechanisms of absorption and distribution, the metabolic changes caused due to that substance in the body, and the routes of excretion of the metabolites of the drug. Pharmacokinetic properties of chemicals are affected by the route and dose of the administered drug. These may affect the absorption rate.

 

  • Track 3-1Pharmacokinetic models
  • Track 3-2Bioavailability
  • Track 3-3Population pharmacokinetics
  • Track 3-4Clinical pharmacokinetics

Pharmacodynamics is the study of physiologic and biochemical effects of drugs. The effects may include those manifested within animals and humans, microorganisms and other organisms. It is the study of how a drug affects an organism, whereas pharmacokinetics is the study of how the organism affects the drug. Both together influence dosing, benefit, and adverse effects.

 

  • Track 4-1Activating drug
  • Track 4-2Drug Dose
  • Track 4-3Desensitization

Pharmacoepidemiology is the study of the effects and uses of drugs in well-defined populations. To do this study, pharmacoepidemiology takes content from pharmacology as well as epidemiology. Thus, it is the bridge between both pharmacology and epidemiology. Pharmacology is defined as studying the effect of drugs and clinical pharmacology is the study of effect of drugs on patients or humans. Clinical pharmacology also provides a risk benefit assessment of effects of drugs in patients.

 

  • Track 5-1Epidemiology
  • Track 5-2Exposome
  • Track 5-3Molecular epidemiology

Biologics are medicines made from living cells by using very complex manufacturing processes and must be handled and administered carefully. Types of biologic drugs are vaccines, blood, recombinant proteins blood components, cells, allergens, genes and tissues. Biologic drugs are used for treating various diseases and conditions, and are the most advanced therapies available. Some biologic drugs are used for the treatment of Crohn's disease, ulcerative colitis, and other autoimmune diseases.

 

  • Track 6-1Vaccines
  • Track 6-2Blood and blood components
  • Track 6-3Allergenics
  • Track 6-4Somatic cells
  • Track 6-5Gene therapy
  • Track 6-6Recombinant therapeutic proteins.

Pharmaceutical packaging is the packaging processes for pharmaceutical preparations. It involves all of the operations from production through drug distribution channels to the end consumer.

Pharmaceutical packaging is highly regulated but there is small variation in the details, depending on the country of origin or the region. The common factors include: assurance of patient safety, thorough documentation of all materials and processes, control of possible migration of packaging components into the drug, control of degradation of the drug by oxygen, moisture, heat, assurance of the efficacy of the drug through the intended shelf life, uniformity of the drug through different production lots etc.

 

  • Track 7-1Package forms
  • Track 7-2Counterfeiting
  • Track 7-3Packaging production
  • Track 7-4Serialization

Physical pharmacy is the branch of pharmacy which focuses on the application of physics and chemistry to the study of pharmacy. It is the study of the effects of dosage forms on their environment by checking them at the molecular level. It emphasis on the actions and physical characteristics of the drug delivery system before it is given to the patient. It forms the basis for design, manufacture, and distribution of drug products and acts as the foundation for the stable and proper use of medical drugs. It covers areas such as solubility, drug delivery and pharmacokinetics.

 

  • Track 8-1Physics
  • Track 8-2Chemistry
  • Track 8-3Drug delivery system
  • Track 8-4Drug absorption
  • Track 8-5Drug metabolism

Pharmaceutical Biotechnology is the science that includes all technologies needed for producing, manufacturing and registration of biological drugs. Biochemistry is the branch of science that explores the chemical processes within the living organisms. It is a laboratory based science that brings chemistry and biology together. Pharmaceutical companies use biotechnology for manufacturing drugs, gene therapy, pharmacogenomics and genetic testing.

 

  • Track 9-1Bio formulations
  • Track 9-2Stability
  • Track 9-3 Toxicity
  • Track 9-4Immunogenicity
  • Track 9-5 Patenting
  • Track 9-6 Clinical trials

Pharmacogenomics is the study of how genes affect a person’s response to drugs. This is a new field and combines pharmacology and genomics to develop effective and safe medications and doses that will be designed according to a person’s genetic organization. The field of pharmacogenomics is still in its early stage. Its use is currently quite limited, but new approaches are under study in clinical trials. 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.

 

  • Track 10-1Genome
  • Track 10-2Drug response
  • Track 10-3Epigenetics
  • Track 10-4Genotyping
  • Track 10-5Genome sequencing
  • Track 10-6Polypharmacy
  • Track 10-7Drug labeling

Pharmacovigilance or drug safety, is the pharmacological science related to the collection, detection, monitoring, assessment, and prevention of adverse effects of pharmaceutical products.

Information received from patients and healthcare providers by pharmacovigilance agreements and other sources like the medical literature, plays an important role in providing the data necessary for pharmacovigilance to take place. In order to market or to test a pharmaceutical product in most countries, adverse event data received by the license holder should be submitted to the local drug regulatory authority.

  • Track 11-1Adverse Drug Reaction
  • Track 11-2Adverse Events
  • Track 11-3Clinical Trials
  • Track 11-4Biological medicines

 Pharmacognosy is the study of the physical, biochemical, chemical and biological properties of drugs, or potential drugs or drug substances of natural origin as well as the search for new drugs from natural sources.

 Pharmacognosy is one of the five major divisions of the pharmaceutical science. It represents the oldest branch of the profession of pharmacy.

 

  • Track 12-1Botany
  • Track 12-2Ethnobotany
  • Track 12-3Zoopharmacognosy
  • Track 12-4Natural products chemistry
  • Track 12-5Herbal practices

Pharmaceutical chemistry is the study of drugs, and it involves drug development. This includes drug discovery, absorption, delivery metabolism etc. It is a mixture of different elements like biomedical analysis, pharmacology, pharmacokinetics, and pharmacodynamics. Pharmaceutical chemistry work is mainly conducted in labs.

Pharmaceutical chemistry involves cures and remedies for disease, analytical techniques, pharmacology, metabolism, and drug chemistry.

  • Track 13-1Organic chemist
  • Track 13-2Combinatorial chemistry
  • Track 13-3Enzymes

Pharmaceutical Nanotechnology is a branch of pharmacy that deals with new emerging technologies for developing customized solutions for drug delivery systems. The drug delivery system affects the rate of absorption, distribution, metabolism, and excretion of the drug or other related chemical substances in the body in a positive way. The drug delivery system also helps in binding of drug to its target receptor and influence that receptor’s signalling and activity.

  • Track 14-1Drug delivery
  • Track 14-2Nanomaterial
  • Track 14-3Diagnostics
  • Track 14-4Prognostic

Bio pharmaceutics studies the relationship between the physical or chemical properties of the drug, the dosage form in which the drug is given, and the route of administration on the rate and extent of systemic drug absorption. The importance of the drug substance and the drug formulation on absorption, and in vivo distribution of the drug to the site of action, is described as a sequence of events that precede elicitation of a drug’s therapeutic effect.

  • Track 15-1Active Pharmaceutical Ingredient
  • Track 15-2Investigational New Drug
  • Track 15-3New Drug Application
  • Track 15-4Drug Form
  • Track 15-5Drug Product
  • Track 15-6Solid Dispersion

 Pharmaceutical jurisprudence is the study of laws regulating the profession of pharmacy. It includes all the acts and rules mentioned in the constitution.
 E.g. drug and Cosmetics act and rules, pharmacy act, MTP act, magic remedies act, etc.

It is important for running a pharma business irrespective of its size, whether it is retail or wholesale or a full-fledged business.

  • Track 16-1Misuse of Drugs
  • Track 16-2Export and Import of Drugs
  • Track 16-3Marketing
  • Track 16-4Administration of Drugs

Pharmaceutical Microbiology is an applied branch of Microbiology. It involves the study of microorganisms associated with the manufacture of pharmaceuticals e.g. minimizing the number of microorganisms in a process environment, excluding microorganisms and microbial bi products like exotoxin and endotoxin and ensuring the finished pharmaceutical product is sterile. Other uses of pharmaceutical microbiology include the research and development of anti-infective agents, the use of microorganisms to detect mutagenic activity in prospective drugs.

 

  • Track 17-1Drug Safety
  • Track 17-2Antimicrobial Activity and Disinfection
  • Track 17-3Microbiologists
  • Track 17-4Cosmetic Microbiology
  • Track 17-5Medical Devices

Industrial Pharmacy is an area which includes manufacturing, development, marketing and distribution of drug products and also quality assurance of these activities. This research area related to different functions in pharmaceutical industry and having contact areas with engineering and economics.

 

  • Track 18-1Fundamentals of Industrial Pharmacy
  • Track 18-2Healthcare Pharmacy
  • Track 18-3Drug Design and Marketing
  • Track 18-4Clinical Studies
  • Track 18-5Waste management of industrial pharmacy
  • Track 18-6Good manufacturing practices

Clinical pharmacy is the area of pharmacy concerned with the science and practice medication use. It includes the provision of patient care with the use of medications to elevate the health outcomes of patients.

  • Track 19-1Personalized Pharmacy Care
  • Track 19-2Clinical Pharmacy and Its Key Role in Treatment
  • Track 19-3Pharmacist in Health Care System
  • Track 19-4Community Pharmacy
  • Track 19-5Latest Advances in Pharmacy Practice

Drug target is the naturally existing cellular structure involved in the pathology of interest that the drug-in-development is meant to act on. It is the process to discover a new drug and bringing a drug to the market once a lead compound has been identified.
Drug discovery and development is an intellectual solution which analyses scientific knowledge and data to reveal known, unknown and hidden connectivity that can help increase the vast possibilities of scientific development. It is used by pharmaceutical companies, medical device companies and academic institutions to assist with new drug target identification and drug re-purposing.

  • Track 20-1Computer-aided drug design
  • Track 20-2Structure-based Drug Design
  • Track 20-3Metabolic Half-Life
  • Track 20-4Bioavailability

Toxicology is a branch of science that helps us understand the harmful effects that chemicals, substances can have on humans, animals, and the environment. Toxicology can also be referred as the “Science of Safety” because as a field it has evolved from a science focused on studying poisons and adverse effects of chemical exposures.
The relationship between dose and its effects on the exposed organism is highly important in toxicology. Factors that influence chemical toxicity include the dosage, route of exposure, species, age, gender and environment. Toxicologists are experts of poisons.

 

  • Track 21-1Medical toxicology
  • Track 21-2Clinical toxicology
  • Track 21-3Toxicologist

Hospital Management is defined from different aspects. It mainly relates to management of all the areas of a hospital; a coordination of all elements of a hospital. This may range from patient care to record keeping to inventory of medicines and cleanliness. To be able to become a hospital management professional requires taking care of each and every element of the hospital.

 

  • Track 22-1Healthcare Management
  • Track 22-2Health Administration
  • Track 22-3Healthcare Information and Management Systems Society

Computer aided design and drafting (CADD) is a subfield of engineering which deals with the design and drafting of drugs through the use of specialized software that visualizes designs as modular 3D computer models.

Computer aided design (CAD) software is used for creating the 3D models complete with detailed documentation such as dimensions, materials used and even details the design process.

 

  • Track 23-1CAD

Pharmaceutical technology is application of scientific knowledge or technology to pharmacy and the pharmaceutical industry. It includes methods, techniques, and instrumentation in the manufacture, preparation, dispensing, packaging, and storing of drugs and other preparations used in determinative procedures and in the treatment of patients.

 

  • Track 24-1Medical Practitioners
  • Track 24-2Drug Inspectors
  • Track 24-3Drug Analysts

It is a branch of pharmacology that deals with the entry of chemicals or drugs into the environment after they are eliminated by humans and animals in post-therapy.

 

  • Track 25-1Climate change
  • Track 25-2Biodiversity loss
  • Track 25-3Water Scarcity
  • Track 25-4The Health Impacts of Pollution