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10th Annual Congress on Drug Formulation & Analytical Techniques , will be organized around the theme “Recent innovations and approaches in Drug Formulation & Analytical techniques ”
Drug Formulation 2018 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Drug Formulation 2018
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Pharmaceutical formulation in pharmaceutics is the process in which various chemical substances including the vigorous drug are joined to produce a final medicinal product. Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patient. For orally taken drugs, this usually contains combining the drug into a tablet or a capsule. Formulations confirm that the drug is compatible with these other substances. In the pharmaceutical drug formulations, the different physical, chemical, and mechanical properties of a drug are considered so as to know what other ingredients should be used in the preparation. The various factors like polymorphism, particle size, pH, and solubility are all considered while formulating the drug, also considering the appearance of the tablet.
- Track 1-1Formulation and pre formulation
- Track 1-2Developing a preparation of the drug
- Track 1-3Formulation types
- Track 1-4Formulation from plant sources
- Track 1-5Quality of Formulation
- Track 1-6Waste management of industrial pharmacy
The drug subjected to drug development undergoes number of trials and are screened at different stages to produce a final potent drug intended for the treatment of various diseases. During this process various properties are checked to see whether the drug is non-toxic to living system and is therapeutic or not. Using suitable excipients and technological preparations the active substances are formulated into final dosage form. The last product is the Actual composition of preparation, manufacturing specification.
- Track 2-1Types of Coating and coating procedures
- Track 2-2Validation process
- Track 2-3Advanced formulation techniques
- Track 2-4Development of Parenteral dosage form
- Track 2-5Development of oral dosage form
- Track 2-6Lyophilized dosage forms
- Track 2-7New chemical entity development
Bioavailability is a subcategory of pharmacological absorption. Bioavailability is generally assessed by finding the area under the plasma concentration–time curve. The factors affecting bioavailability are Pharmaceutics factors, physicochemical properties of drug, Dosage form characteristics & Pharmaceutic Ingredients, Patient related factors like age, Routes of administration (Parenteral, Rectal, Oral, and Topical) etc.
Conducting a BA study enables assessment of the impact of route of administration on BA and defines the absolute BA of the drug released from the drug product. BA for a given formulation provides an assessment of the relative fraction of the orally administered dose that is absorbed into the systemic circulation. If the reference standard is an IV dose, it is referred as Absolute Bioavailability. If the reference standard is any other dosage form than IV it is referred as Relative Bioavailability
- Track 4-1 Drug Metabolism
- Track 4-2 Pharmacology- PK & PD approach
- Track 4-3Mineral Bioavailability- Micro and Macro
- Track 4-4 Biowaivers: Criteria
- Track 4-5BCS & IVIVC Based Biowaivers
- Track 4-6BCS & IVIVC Based Biowaivers
- Track 4-7Recent approaches to Biosimilars
The primary scope of toxicological studies in the drug development process is to estimate the safety of potential drugs. This is proficient using relevant animal models and validated procedures. The ultimate goal is to translate the animal model responses into an understanding of the risk for the human subjects. The drug toxicology plays a very important role in evaluating the safety of the drug.
- Track 5-1Drug Safety Biomarkers
- Track 5-2Predictive Toxicology
- Track 5-3Toxicological Testing
- Track 5-4Preclinical Drug Development
- Track 5-5Preclinical Safety Assessment
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.
The U.S. pharmaceutical market is the world’s most important national market. Together with Canada and Mexico, it represents the largest continental Pharma market worldwide. The United States alone holds some 40 percent of the global pharmaceutical market. In 2014, this share was valued around 365 million U.S. dollars. Many of the global top companies are located in the United States. In 2014, six out of the top eleven companies were U.S.-based.
- Track 6-1Fundamentals of Industrial Pharmacy
- Track 6-2Healthcare pharmacy
- Track 6-3Drug Design and Marketing
- Track 6-4Veterinary Pharmaceuticals
- Track 6-5Pharmacy from Natural products
- Track 6-6Market surveillance of industrial pharmacy
Analytical method development is the process of choosing an accurate assay procedure to determine the composition of a formulation. It is the process of proving that an analytical method is acceptable for use in laboratory to measure the concentration of subsequent samples Analytical methods should be recycled within GMP and GLP environments and must be developed using the protocols and acceptance conditions set out in the ICH guidelines. Analytical method development and validation stand the continuous and inter-dependent task associated with the research and development, quality control and quality assurance departments. Analytical procedures play a critical role in equivalence and risk assessment, management. It supports in formation of product-specific acceptance criteria and stability of results. Validation should establish that the analytical procedure is suitable for its intented purpose. Design of experiment is a powerful tool for the method characterization and validation.
- Track 7-1Electroanalytical methods
- Track 7-2chemical analytical methods
- Track 7-3analytical research methodology
- Track 7-4Analytical methods and biomarker validation
- Track 7-5HPLC analytical method development and validation
- Track 7-6Drug screening: Strategy and methods
- Track 7-7Forensic analytical techniques
- Track 7-8Nanotechnology applications in analytical methods
- Track 7-9Fluorescence techniques
- Track 7-10analytical marketing
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 8-1RNA and DNA Nanotechnology
- Track 8-2Pharmaceutical Nanotechnology based Systems
- Track 8-3Organic Agriculture and Nanotechnology
- Track 8-4Screening and design
- Track 8-5Engineering of Pharmaceutical Nanosystems
- Track 8-6Current Research in Nanotechnology
- Track 8-7Nanotechnogy methods in Drug Design
- Track 8-8Future Prospects of Pharmaceutical Nanotechnology
Analytical chemistry, as the component of chemistry most diligently related to engineering, most involved in the development of new instrumentation and new technology, and most concerned with the applied applications of chemistry, has seen increased attention with the emergence of the mega-interdisciplinary parts of nanotechnology and systems biology.
- Track 9-1Analytical Techniques in Chemical Engineering
- Track 9-2Chemical Engineering
- Track 9-3Pharmaceutical Chemistry and Engineering
- Track 9-4Pharmaceutical Analytical Chemistry
Chromatography and mass qualitative analysis is employed for analysis of organic compounds. Electro spray ionization (ESI) could be a method employed in mass spectroscopic analysis. As relate to chromatography and mass spectrometry .HPLC is further flexible informative and trusted by the industry people. Recent advances in sample preparation techniques to beat difficulties encountered throughout measuring of little molecules from bio fluids mistreatment LC-MS. For Measuring, observation and protective your important Investments analytical chemistry instruments are used. Global Bioanalysis seminars are conducted and those specifically applied for chromatography assays, ligand binding assays to know more advances.
- Track 10-1Gas Chromatography
- Track 10-2Liquid Chromatography
- Track 10-3HPLC and Applications
- Track 10-4Mass spectrometry for biomedical applications
- Track 10-5MALDI imaging mass spectrometry
- Track 10-6Proteomic and mass spectrometry technologies for biomarker discovery
- Track 10-7Electrospray ionization
- Track 10-8Advances in sample preparation
- Track 10-9Advances in Analytical Chemistry Instrumentation
Analytical chemistry is that the study of the separation, identification, quality control and quality assurance of the chemical parts of natural and artificial materials .The maintenance of a desired level of quality in an exceptionally package or product, particularly by resources that of attention to every one stage of the method of delivery or production. Bioanalytical Chemistry could be a sub-division of Analytical Chemistry that refuges the measuring of medicine, Ion sensors, Proteins and DNA Sequences in unnatural samples or concentrations. Accurate quantification of the drug samples is extremely very important for several scientific endeavours which can not delay the result. Therefore the Bioanalytical Techniques are in the main focussed to bring the correct results of the drug sample to supply an ideal result.
- Track 11-1Method development and validation reports
- Track 11-2DNA sequencing
- Track 11-3Ion sensors
- Track 11-4Quality assurance in analytical chemistry
- Track 11-5Recent advances in emerging imaging techniques
NMR analysis is recycled in separation of complex l and natural samples. Recent advances in mass chemical analysis part unit facultative improved analysis of endogenous metabolites. Here we have a tendency to deliberate many problems relevant to developing High-Performance Liquid Chromatography, electro spray ionization, mass chemical analysis conducts for targeted metabolomics (i.e., menstruation of dozens to many specific metabolites).Lab-on-a-chip devices range unit a set of MEMS instruments and infrequently indicated by "Micro Total Analysis Systems" (µTAS) still.
- Track 12-1Analytical and preparative instrumentation
- Track 12-2LC‐MS‐based nontargeted metabolomics
- Track 12-3Analytical instruments for nanomaterial characterization
- Track 12-4New trends in the analytical determination of emerging contaminants
- Track 12-5Lab-on-a-chip device applications
- Track 12-6Preparation automation for GC injection
- Track 12-7NMR analysis of complex natural samples
Bioanalysis may be a sub-discipline of analytical chemistry covering the quantitative action of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotic (macro and micro molecules, proteins, DNA, giant molecule medicine, metabolites) in biological structures. Applications for analytical and Bioanalytical method development and validation, are as follows: biological safety test, clinical support, separation of mixture of compound, drug analysis. Prominence of understanding proteomics and process of food science is essential, and can be discussed by using separation techniques.
- Track 13-1Chemometrics, marine products, and food science
- Track 13-2Advances in micro/nano-bioanalysis
- Track 13-3Micro and nano technologies in bioanalysis
- Track 13-4Method Development and validation reports
Bioanalytical Chemistry may be a sub-division of Analytical Chemistry that covers the measuring of medicine, Proteins and de oxy ribonucleic acid in unnatural samples or concentrations. In the Previous times, Bio analysis was supposed to be used for the measuring of little drug molecules, How ever since the explosion of biopharmaceuticals has started. Bioanalytical Techniques and validation are utilized in the measuring and analysis of huge molecule medicine. Bio analytical Chemistry improvement mostly started by the usage of the recently developed understated strategies that include: combined techniques like Chromatography, LC-MS, Spectroscopy and ultrafast spectroscopy, GC-MS and natural process strategies like HPLC.
- Track 14-1Chromatographic methods
- Track 14-2Spectroscopy and ultrafast spectroscopy
- Track 14-3Bioanalytical method validation
- Track 14-4Molecular and functional imaging
- Track 14-5Diverse applications: Biologics, diagnostics, and toxicology
- Track 14-6Electrophoresis/ligand binding assay
- Track 14-7Bioanalytical Services And Research
- Track 14-8Advances in Bioanalytics, Biomarkers and Diagnostics
- Track 14-9Bioanalytical Method Development and Validation
- Track 14-10Analytical proteomics and metabolomics
- Track 14-11Microscopy, hybrid methods, and thermal analysis
- Track 14-12InfraRed (IR) spectroscopy
In bioscience and drugs, to a small grade molecule may be a coffee mass (<900 Daltons ) compound which is incapable to facilitate regulate a process, with a size on the order of 10−9 m. Most drug analysis square measure identical little molecules. For analysis of small organic molecules the subsequent devices ought to be recycled are as follows HPLC method, chromatography, Ultraviolet-visible (UV-VIS) spectrophotometry, Infrared (IR) spectrometry and mass spectrometry.
- Track 15-1NMR techniques in organic chemistry
- Track 15-2Current Brain research with NMR spectroscopy
- Track 15-3Advanced medical imaging techniques (MRI)
- Track 15-4Ultraviolet-visible (UV-VIS) spectrophotometry
- Track 15-5Mass spectrometry in the analysis of small organic molecules
Analytical techniques transform researchers to look at complicated relationships between variables and those methods are Regression Analysis, Grouping ways, Multiple Equation Models.Chemistry that involves the study of the molecular mechanisms fundamental the performance of the system, particularly the character of antibodies, antigens and their interactions. The foremost common diagnostic ways include: diagnostic assay, Endoscopy, Diagnostic Imaging, Blood Tests, immunochemical assay. The tremendous molecule detected by the bioassay is usually remarked as Associate in Nursing "analyte" and is in several cases a macromolecule. Analytes in biological liquids identical body fluid or area unit often measured abuse immuno assays for medical and analysis functions.
- Track 16-1Techniques for cancer diagnostics
- Track 16-2Immunological assays
- Track 16-3Modern immunochemical methods
- Track 16-4Immunoanalytical techniques
- Track 16-5Electrochemical immunosensor
Environmental analytical chemistry is the scientific study of the chemical and organic chemistry phenomena that occur in natural places. Environmental chemistry is that the scientific study of the chemical and chemical science phenomena that occur in natural places. Quantitative & qualitative analysis may be a key a part of environmental chemistry, since it provides the information that frame most environmental studies or environment pollution studies. Common analytical techniques used for quantitative determinations in environmental chemistry embody classical wet chemistry, like menstruation, titrimetric and chemistry strategies. Sometimes due to climate changes in the atmosphere pests attaches the crops. To avoid loss of fertility and food safety in crops pesticides are used.
- Track 17-1Environmental analysis: Emerging pollutants
- Track 17-2Pesticide and biopesticide analysis
- Track 17-3Residue levels in agricultural products and food safety
- Track 17-4Methods for environmental trace analysis-atmospheric chemistry
- Track 17-5Bioavailability, bioaccessibility and mobility of environmental contaminants
- Track 17-6Environmental chemistry
- Track 17-7Environmental Analytical Chemistry
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)
Regulatory affairs (medical affairs) professionals (aka regulatory professionals) usually have responsibility for the following general areas: Ensuring that their companies comply with all of the regulations and laws pertaining to their business, Working with federal, state and local regulatory agencies and personnel on specific issues affecting their business. i.e. working with such agencies as the Food and Drug Administration or European Medicines Agency (pharmaceuticals and medical devices); The Department of Energy; or the Securities and Exchange Commission (banking), Advising their companies on the regulatory aspects and climate that would affect proposed activities. i.e. describing the "regulatory climate" around issues such as the promotion of prescription drugs and Sarbanes-Oxley compliance.
- Track 18-1Pharmacovigilance Regulations
- Track 18-2Regulatory Strategies and Developments
- Track 18-3Clinical Affairs & Regulatory Strategies
- Track 18-4SOPs and Policy Documents
- Track 18-5Regulatory & Pharmacovigilance
- Track 18-6Global Regulatory Intelligence
- Track 18-7Regulatory Communications and Submissions
- Track 18-8Regulatory Requirements for Pharmaceuticals
- Track 18-9Medical Device & Combination Products Regulations
- Track 18-10Best Industry Practices
- Track 18-11Marketing Authorizations
- Track 18-12Regulatory Challenges for Medical Devices
- Track 18-13Food, drug and cosmetic laws
- Track 18-14FDA and related regulatory agencies
- Track 18-15Data Integrity towards Regulatory Affairs