Track Categories

The track category is the heading under which your abstract will be reviewed and later published in the conference printed matters if accepted. During the submission process, you will be asked to select one track category for your abstract.

Innovations used to perform bioanalytical techniques change as indicated by the sub-atomic substance's tendency. With compound products, the organic parts of test samples can be evacuated by precipitation or extraction, permitting remaining little molecule (s) to be analyzed with advances, for example, LC–MS or GC–MS. With biomolecular products (or antiproduct antibodies), processing away the organic parts of a sample can similarly expel the objective analyte, making precise quantitation technically impossible. So for biotech products and antiproduct antibodies, bioanalytical methods require advances that can particularly gauge one biological moiety (the protein(s) of interest) within the sight of a biological milieu (which contains numerous proteins).

Immunological techniques that utilizes particular antigen-antibody recognition (e.g., ELISA-like  methods) are typically opted for bioanalytical assays applied to biopharmaceutical products since they can angle the one protein of interest out of the protein blend. Similarly, immunogenicity screening tests utilize ELISA-like methods to catch receptive immunoglobulins. Maybe the disarray between bioanalytical methods and analytical methods utilized for the testing of biomolecular products" is more pervasive in the biopharmaceutical community in light of the way of our products. The most exact term for the analytical methods used to evaluate the physiochemical parameters of these products is thought by many to be biomolecular methods.

  • Track 1-1 Method development and validation reports
  • Track 1-2 DNA sequencing
  • Track 1-3 Ion sensors
  • Track 1-4 Quality assurance in analytical chemistry
  • Track 1-5 Recent advances in emerging imaging techniques

An analytical method is a gathering of set focuses required to run a solitary example on the 6890 Series GC. Techniques make it conceivable to re-establish the instrument to a coveted setup without returning all the set-points. You can think about a strategy as a gathering of finished control tables, containing data, for example, oven temperature programs, pressure programs, inlet temperatures, and so forth. Really, there is dependably a dynamic technique in the GC. It is the arrangement of conditions that are controlling the machine now. It can be reloaded any time. Analytical methadology incorporates fluorescence imaging has been utilized generally in cell science to concentrate cell structures and procedures, especially in living cells. Electro Analytical Techniques: Electroanalytical methods offer a novel access to data on compound, biochemical, and physical frameworks. Both the instrumental basis and the theoretical fundamentals have been created with the end goal that non-experts can easily apply them. Nanotechnology applications in scientific strategies Modern analytical chemistry is commanded by instrumental analysis where the emphasis is on the single sort of instrument. Over the previous decade, the scientific and technological intrigue has moved from the perceptible to the nanoscopic measure level. With the expanding requirement for portraying materials, it is essential to break down neighborhood contrasts in the structure and piece of nanomaterials. Drug screening: Strategy and techniques. Analytical methods must be approved to give dependable information to regulatory submissions. These techniques are fundamental for various purposes, including testing for QC discharge, testing of security tests, testing of reference materials and to give information to provide data to support specifications.

  • Track 2-1 Fluorescence techniques
  • Track 2-2 Electro analytical techniques
  • Track 2-3 Nanotechnology applications in analytical methods
  • Track 2-4 HPLC analytical method development and validation
  • Track 2-5 Drug screening: strategy and methods
  • Track 2-6 Analytical methods and biomarker validation
  • Track 2-7 Analytical research methodology
  • Track 2-8 Chemical analytical methods
  • Track 2-9 Analytical marketing
  • Track 2-10 Analytical equipment in business

The advancement of the bioanalytical methodology brought a dynamic discipline for which the future holds many energizing opportunities to further advancements. The principle effect of bionalysis in the pharmaceutical area is to acquire a quantitative measure of the drug and its metabolites. The reason for existing is to play out the pharmacokinetics, toxicokinetics, bioequivalence and presentation reaction like pharmacokinetic/pharmacodynamic examines. Different bioanalytical systems are performed in bioanalytical studies, for example, hyphenated methods, chromatographic methods, and ligand bioanalytical strategies. This audit widely highlights the part of bioanalytical methods and hyphenated instruments in evaluating the bioanalysis of the medications.

  • Track 3-1 Chromatographic methods
  • Track 3-2 Bioanalytical services and research
  • Track 3-3 Diverse applications: biologics, diagnostics, and toxicology
  • Track 3-4 Bioanalytical method validation
  • Track 3-5 Spectroscopy and ultrafast spectroscopy
  • Track 3-6 Microscopy, hybrid methods, and thermal analysis
  • Track 3-7 Analytical proteomics and metabolomics
  • Track 3-8 Bioanalytical method development and validation
  • Track 3-9 Advances in bioanalytics, biomarkers and diagnostics

Chromatography is a laboratory technique for the separation of a mixture. 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 affect the separation. Chromatography may be preparative or analytical. The purpose of preparative chromatography is to separate the components of a mixture for later use, and is thus a form of purification. Analytical chromatography is done normally with smaller amounts of material and is for establishing the presence or measuring the relative proportions of analytes in a mixture. The two are not mutually exclusive.

  • Track 4-1 Gas chromatography
  • Track 4-2 Chiral columns chromatography
  • Track 4-3 Thin layer chromatography
  • Track 4-4 Ion exchange chromatography
  • Track 4-5 Affinity chromatography
  • Track 4-6 Two-dimensional chromatography
  • Track 4-7 Pyrolysis gas chromatography
  • Track 4-8 Aqueous normal phase chromatography

Environmental Analytical Chemistry concentrate on specialization in advanced modern analytical methodology to confront different difficulties in environmental and pharmaceutical industry. The Journal covers zone, for example, analytical instrumentation techniques for remote estimations, assurance of trace atmospheric constituents of anthropogenic and characteristic root, location and ID of natural and inorganic poisons in air, water, soil determination and validation of substantial metals and radionuclides in the environment, diverse technique of chemometrics in ecological examination. Instances of issues which have been tended to by climatic science consolidate destructive rain, ozone consumption, photochemical fumes cloud, greenhouse gases and a global warming. Environmental chemistry includes some points that incorporates astrochemistry, environmental science, ecological demonstration, geochemistry, marine chemistry and pollution remediation.

  • Track 5-1 Environmental monitoring
  • Track 5-2 Environmental chemistry and engineering
  • Track 5-3 Freshwater environmental quality parameters
  • Track 5-4 Environmental toxicology and mutagenicity

The development of particles under spatially uniform electric field in a liquid is called electrophoresis. It is caused by a charged interface show between the molecule surface and the encompassing liquid. The rate of movement of molecule relies on upon the quality of the field, on the net charge size and state of the particles and furthermore on the ionic quality, consistency and temperature of medium in which the atoms are moving. As an analytical tool, electrophoresis is straightforward, fast and exceedingly sensitive. It is utilized scientifically to concentrate the properties of a solitary charged species and as a separation technique. It gives the premise to various analytical techniques utilized for isolating atoms by size, charge, or restricting fondness. Example for the partition of deoxyribonucleic corrosive (DNA), ribonucleic corrosive (RNA), or protein particles utilizing an electric field connected to a gel framework. Gel framework utilized primarily is polyacrylamide and agarose. DNA Gel electrophoresis is generally performed for investigative purposes, regularly after intensification of DNA by means of PCR, yet might be utilized as a preparative technique before utilization of different techniques, for example: mass spectrometry, RFLP, PCR, cloning, DNA sequencing or Southern blotching for further characterization.

  • Track 6-1 Affinity electrophoresis
  • Track 6-2 Dielectrophoresis
  • Track 6-3 Gel electrophoresis
  • Track 6-4 Immunoelectrophoresis
  • Track 6-5 Isotachophoresis
  • Track 6-6 Electrochromatography
  • Track 6-7 Protein electrophoresis
  • Track 6-8 NMR and analysis of small organic molecules

Mass spectrometry is a powerful analytical method used to assess known materials, to perceive obscure mixes inside an illustration and to clarify the structure and compound properties of various particles. The aggregate method incorporates the change of the example into vaporous particles, with or without fracture, which are then described by their mass to charge extents (m/z) and relative abundances. This technique essentially concentrates the impact of ionizing energy on particles. It relies on substance responses in the gas phase in which sample molecules are devoured amid the arrangement of ionic and neutral species. A mass spectrometer creates various particles from the specimen under scrutiny, it then isolates them as per their particular specific mass-to-charge ratio (m/z), and afterward records the relative abundance of each ion type. The initial phase in the mass spectrometric examination of mixes is the creation of gas stage particles of the compound, fundamentally by electron ionization. This atomic particle experiences fragmentation. Every essential item particle gotten from the atomic particle, thusly, experiences fragmentation and so on. The particles are isolated in the mass spectrometer as per their mass-to-charge proportion, A mass range of the atom is subsequently created. It shows the outcome as a plot of particle plenitude versus mass-to-charge proportion. Particles give data concerning the nature and the structure of their antecedent atom. In the range of an unadulterated intensify, the atomic particle, if show, shows up at the most noteworthy estimation of m/z (trailed by particles containing heavier isotopes) and gives the sub-atomic mass of the compound.

  • Track 7-1 Helium mass spectrometer
  • Track 7-2 Ion attachment mass spectrometry
  • Track 7-3 MALDI imaging
  • Track 7-4 Membrane introduction mass spectrometry
  • Track 7-5 Electron spectrometer
  • Track 7-6 Atom probe

Crystallography, branch of science that deals with discerning the arrangement and bonding of atoms in crystalline solids and with the geometric structure of crystal lattices. Classically, the optical properties of crystals were of value in mineralogy and chemistry for the identification of substances. Modern crystallography is largely based on the analysis of the diffraction of X-rays by crystals acting as optical gratings. Using X-ray crystallography, chemists are able to determine the internal structures and bonding arrangements of minerals and molecules, including the structures of large complex molecules, such as proteins and DNA.

  • Track 8-1 Crystal engineering
  • Track 8-2 Crystal optics
  • Track 8-3 Crystallization processes
  • Track 8-4 Crystallographic group
  • Track 8-5 Diffraction
  • Track 8-6 Electron crystallography
  • Track 8-7 Molecular modelling
  • Track 8-8 Powder diffraction
  • Track 8-9 X-ray crystallography

Spectroscopy is the study of the interaction between matter and electromagnetic radiation. Historically, spectroscopy originated through the study of visible light dispersed according to its wavelength, by a prism. Later the concept was expanded greatly to include any interaction with radiative energy as a function of its wavelength or frequency. Spectroscopic data are often represented by an emission spectrum, a plot of the response of interest as a function of wavelength or frequency. Spectroscopy and spectrography are terms used to refer to the measurement of radiation intensity as a function of wavelength and are often used to describe experimental spectroscopic methods. Spectral measurement devices are referred to as spectrometers, spectrophotometers, spectrographs or spectral analyzers.

  • Track 9-1 Coherent spectroscopy
  • Track 9-2 EPR spectroscopy
  • Track 9-3 Laser-induced breakdown spectroscopy (LIBS)
  • Track 9-4 Scanning tunneling spectroscopy
  • Track 9-5 Spectrophotometry
  • Track 9-6 Atomic absorption spectrophotometry
  • Track 9-7 Quantification of nucleic acids
  • Track 9-8 Vibrational spectroscopy

Analytical chemistry is also focused on improvements in experimental design, chemometrics, and the creation of new measurement tools to provide better chemical information. Analytical chemistry has applications in forensics, bioanalysis, clinical analysis, environmental analysis, and materials analysis.

The instruments and techniques developed by the physicist for the determination of physical constants have furnished the chemical analyst with new devices which can be used for the quantitative and qualitative determination of the elementary composition of substances. These new methods have supplemented the classical methods of gravimetric and volumetric analysis which experienced their greatest growth during the nineteenth century. The physical methods have enabled the analyst to broaden the scope of analysis, since in many cases accurate measurements can be made without destruction of the sample. He is also able to analyze complex mixtures quantitatively, which previously would have presented almost unsurmountable difficulties. The analyst now has at his disposal physical methods which enable him to investigate problems of structure in organic chemistry, reaction kinetics, and even the biochemistry of living cells.

  • Track 10-1 Spectroscopy
  • Track 10-2 Mass Spectrometry
  • Track 10-3 Electrochemical analysis
  • Track 10-4 Thermal analysis
  • Track 10-5 Separation
  • Track 10-6 Hybrid techniques
  • Track 10-7 Microscopy
  • Track 10-8 Lab-on-Chip

Nuclear Magnetic Resonance (NMR) spectroscopy is an analytical chemistry technique used in quality control and research for determining the content and purity of a sample as well as its molecular structure. For example, NMR can quantitatively analyze mixtures containing known compounds. For unknown compounds, NMR can either be used to match against spectral libraries or to infer the basic structure directly. Once the basic structure is known, NMR can be used to determine molecular conformation in solution as well as studying physical properties at the molecular level such as conformational exchange, phase changes, solubility, and diffusion.

  • Track 11-1 NMR techniques
  • Track 11-2 Correlation spectroscopy
  • Track 11-3 Solid-state nuclear magnetic resonance
  • Track 11-4 Biomolecular NMR spectroscopy

Titration, process of chemical analysis in which the quantity of some constituent of a sample is determined by adding to the measured sample an exactly known quantity of another substance with which the desired constituent reacts in a definite, known proportion. The process is usually carried out by gradually adding a standard solution (i.e., a solution of known concentration) of titrating reagent, or titrant, from a burette, essentially a long, graduated measuring tube with a stopcock and a delivery tube at its lower end. The addition is stopped when the equivalence point is reached.

  • Track 12-1 Assay
  • Track 12-2 Acid-base titration
  • Track 12-3 Complexometric titration
  • Track 12-4 Karl Fischer titration
  • Track 12-5 Nonaqueous titration
  • Track 12-6 Redox titration
  • Track 12-7 Thermometric titration
  • Track 12-8 Sorensen formol titration
  • Track 12-9 Redox indicator

Analytical chemistry has applications including in forensic science, bioanalysis, clinical analysis, environmental analysis, and materials analysis. Analytical chemistry research is largely driven by performance (sensitivity, detection limit, selectivity, robustness, dynamic range, linear range, accuracy, precision, and speed), and cost (purchase, operation, training, time, and space). Among the main branches of contemporary analytical atomic spectrometry, the most widespread and universal are optical and mass spectrometry. In the direct elemental analysis of solid samples, the new leaders are laser-induced breakdown and laser ablation mass spectrometry, and the related techniques with transfer of the laser ablation products into inductively coupled plasma. Advances in design of diode lasers and optical parametric oscillators promote developments in fluorescence and ionization spectrometry and also in absorption techniques where uses of optical cavities for increased effective absorption pathlength are expected to expand. The use of plasma- and laser-based methods is increasing. An interest towards absolute (standardless) analysis has revived, particularly in emission spectrometry.

  • Track 13-1 Forensic science
  • Track 13-2 Bioanalysis
  • Track 13-3 Clinical analysis
  • Track 13-4 Environmental analysis
  • Track 13-5 Materials analysis

The focus of proteomics is a biological group called the proteome. The proteome is dynamic, defined as the set of proteins expressed in a specific cell, given a particular set of conditions. Within a given human proteome, the number of proteins can be as large as 2million.  Proteins themselves are macromolecules: long chains of amino acids. This amino acid chain is constructed when the cellular machinery of the ribosome translates RNA transcripts from DNA in the cell's nucleus.  The transfer of information within cells commonly follows this path, from DNA to RNA to protein.

  • Track 14-1 Limitations of proteomics
  • Track 14-2 High-throughput proteomic technologies
  • Track 14-3 Applications of proteomics
  • Track 14-4 Bioinformatics for proteomics
  • Track 14-5 Modern Trends in proteomics

A scope of analytical tools and systems are utilized in the revelation of confirmation or examination of materials significant to the examination of wrongdoings or to other legitimate procedures. Such measurable confirmation may appear as organic examples, saved follow materials and build-ups or contaminant, fake or lie materials. Analytical instrumentation utilized as a part of measurable reviews has developed to end up noticeably always touchy and give novel data and expanding levels of detail, opening up new potential outcomes in lawful examinations. Morphologically directed Raman Spectroscopy (MDRS) consolidates robotized molecule imaging and Raman spectroscopy in one instrument. Gives size and shape examination alongside substance indentification, which makes the system important for separating between different segments inside a blend or for the discovery of contaminant particles in an example- An unmistakable mark is given that can help distinguish a protest or substance, decide its source or identify changes to its uprightness coming about because of sullying. Coordinate fare of the Raman range of an obscure molecule from Malvern's Morphologi G3-ID programming to Bio-Rad's Know it by all ID Expert, with its broad substance database, upgrades the data picked up by MDRS.

  • Track 15-1 Forensic anthropology
  • Track 15-2 Forensic engineering
  • Track 15-3 Computational forensics
  • Track 15-4 Forensic entomology

A separation procedure is a technique to accomplish any phenomenon that changes over a blend of synthetic substance into  two or more distinct product mixtures, which might be alluded to as mixture. No less than one of which is enhanced in at least one of the mixture's constituents. Now and again, a separation may completely partition the  mixture into its  pure constituents. separation vary in synthetic properties or physical properties, for example size, shape, mass, density, or chemical affinity, between the constituents of a mixture. They are frequently characterized by the specific contrasts they use to accomplish separation. For the most part there is just physical development and no generous synthetic modification. In the event that no single distinction can be utilized to fulfill a desired separation, numerous operations will regularly be performed in combination to accomplish the desired end. With a couple of special cases, components or mixes are normally found in a tainted state. Frequently these tainted crude materials must be isolated into their refined segments before they can be put to productive use, making separation techniques essential for the modern industrial economy. On occasion, these partitions require total purification, as in the electrolysis refining of bauxite mineral for aluminum metal, yet a fair instance of a inadequate separation method is oil refining.  Crude oil occurs naturally as a mixture of different hydrocarbons and debasements. The refining procedure splits this mixture into other, more significant mixtures, for example, flammable gas, fuel and compound feedstocks, none of which are pure substances, yet each of which must be isolated from the crude unrefined. In both of these cases, a progression of separations is important to acquire the desired finished results. On account of oil refining, crude is subjected to a long arrangement of individual refining steps, each of which creates a different product or intermediate.

  • Track 16-1 Filtration and distillation
  • Track 16-2 Chromatography as a separation technique
  • Track 16-3 Applications of separation techniques
  • Track 16-4 Advancements in sample preparation techniques

Current analytical biotechnology is centered around the utilization of an arrangement of empowering stage advancements that give contemporary best in class instruments for genomics, proteomics, metabolomics, tranquilize revelation, screening and investigation of regular item particles. Along these lines, logical biotechnology covers all regions of bioanalysis from biochips and nanochemistry to science and high throughput screening.  Additionally, it intends to apply propelled robotization and smaller scale fabrication innovation to the advancement of mechanical and fluidic gadgets and coordinated frameworks. Significant stages are the utilization of immobilized particles in biotechnology and bioanalysis, immunological procedures, immunological strip tests, fluorescence identification and confocal methods, optical and electrochemical biosensors, biochips, smaller scale specking, novel transducers, for example, nano bunches, nuclear constrain microscopy based strategies and examination in complex media, for example, maturation juices, plasma and serum.

  • Track 17-1 Raman spectroscopy
  • Track 17-2 FTIR
  • Track 17-3 BIOASSAY
  • Track 17-4 X-Ray crystallography

Pharmaceutical analysis is a branch of practical chemistry that includes a progression of process for distinguishing proof, assurance, measurement and decontamination of a substance, partition of the segments of an answer or blend or assurance of structure of synthetic mixes. The substance might be a solitary compound or a blend of mixes and it might be in any of the dose shape. The substance utilized as pharmaceuticals are creatures, plants, small scale living beings, minerals and different manufactured items.  The specimen to be analysed is called as analyse and on the premise of size of test, they can be delegated macro(0.1 g or more), semi miniaturized scale (0.01 g to 0.1 g), micro(0.001 g to 0.01 g), sub smaller scale (0.0001 g to 0.001 g), ultramicro (underneath 10-4 g), follow analysis(100 to 10000 ppm). Among all, the semi smaller scale analysis is broadly utilized.

  • Track 18-1 Absorption spectroscopy in pharmaceutical analysis
  • Track 18-2 Modern pharmaceutical analysis
  • Track 18-3 Pharmaceutical nanotechnology

Process analytical chemistry resembles process analytical technology for example used for the pharmaceutical industry has its beginnings as a specific sort of analytical chemistry used for the technique production. The synthetic procedures are for generation and quality control of fabricated products, and process analytical technology is utilized to decide the physical and chemical composition of the desired items during a manufacturing process. The chemical processes are for production and quality control of manufactured products and for generation and quality control of fabricated items, and process analytical technology is utilized to decide the physical and synthetic composition of the desired items during a manufacturing process.  Process analysis at first included inspecting the assortment of process streams or networks and transporting tests to quality control or central analytical administration research centers. Time delays for analytical results outcomes because of sample transport and analytical preparation steps nullified the estimation of numerous chemical analyses for purposes other than product discharge. After some time it was comprehended that real-time measurements gave convenient data about a process, which was significantly more valuable for  high efficiency and quality. The development of real-time process analysis has provided data to process optimization during any manufacturing process.

  • Track 19-1 Micro-analytical systems
  • Track 19-2 Nanotechnology
  • Track 19-3 Chemometrics
  • Track 19-4 Flow injection analysis 

A branch of materials science where the properties of materials are considered as they change with temperature is what thermal analysis means. A few techniques are normally utilized – these are recognized from each other by the property which is measured: Dielectric thermal analysis (DEA), dielectric permittivity and loss factor. Types of thermal analysis: Dielectric thermal analysis, Differential thermal analysis, Differential Scanning Calorimetry, Dilatometry, Dynamic Mechanical Analysis, Evolved Gas Analysis, Laser flash analysis, thermogravimetric analysis, Thermomechanical Analysis, Thermo-optical analysis and Derivatography.

Glycomic analysis look to see how a gathering of glycans identifies with a specific natural event. Glycomes can far surpass proteomes and transcriptomes regarding complexity.some gauges have set the vertebrate glycome at more than one million discrete structures. Many parts of glycobiology can be seen just with a frameworks level analysis. glycomic changes amid improvement and cancer progression. many GBPs are oligomerized on cells and connect with multivalent varieties of glycans on restricting cells.multiple discrete glycan epitopes work in show to draw in two cells or convey a flag from one cell to the next. The accompanying are cases of the usually utilized methods in glycan analysis: High-resolution mass spectrometry and high-performance liquid chromatography. Multiple Reaction Monitoring. Apparatuses for glycoproteins X-beam crystallography and nuclear magnetic resonance spectroscopy for complete structural analysis of complex glycans is a troublesome and complex field. However the structure of the coupling site of various lectins, catalysts and other starch restricting proteins has uncovered a wide assortment of the basic reason for glycome work.

  • Track 20-1 Dilatometry
  • Track 20-2 Evolved gas analysis (EGA)
  • Track 20-3 Multiple reaction monitoring
  • Track 20-4 Glycoproteins
  • Track 20-5 Metabolomics

Applications of Analytical and Bioanalytical Methods would discuss more about Chemometrics, marine products, and food science, Advances in micro/nano-bioanalysis, Micro and nano technologies in bioanalysis, Method development and validation reports. Advances in micro/nano-bioanalysis: the recent research stream focuses on the integration of chemical functions using various immobilization or patterning techniques, and fusion with nano-scale materials/molecules described above or conventional micro analytical techniques such as flow injection analysis, capillary electrophoresis, and  micro electrodes.To create valuable micro bioanalytical devices, such as  single-cell analysis devices or high-performance diagnosis devices. Micro and nano technologies in bioanalysis: The current improvement of bioanalytical techniques including the improvement of exceedingly delicate or selective analytical methods in view of nano-scale materials/molecules, and the advancement of new analytical tools or methods based on micro/nano-devices have progressed with remarkable success. Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. Pharmaceutical products formulated with more than one drug, typically referred to as combination products, are intended to meet previously unmet patients need by combining the therapeutic effects of two or more drugs in one product. These combination products can exhibit overwhelming difficulties to the analytical chemist in charge of the development and validation of analytical methods.

  • Track 21-1 Micro and nano technologies in bioanalysis
  • Track 21-2 Method development and validation reports
  • Track 21-3 Chemometrics, marine products, and food Science
  • Track 21-4 Advances in micro/nano-bioanalysis

Analytical instruments are used in a variety of fields, given their cross-discipline compatibility to analyze samples. Analytical instruments are used not only in the laboratory environment, but also on the field. They include, but are not limited to the following areas: Analytical Chemistry, Clinical Analysis, Environmental Testing, Food & Beverage Analysis, Forensic Analysis, Life Science Research (e.g. metabolomics, genomics, proteomics), Materials Characterization and Research, Petrochemical Testing, Pharmaceutical Analysis and more. Analytical instrumentation includes those used within spectroscopy, mass spectrometry, electrochemical analysis, thermal analysis, separation analysis, microscopy, and the various hybrid technologies (e.g. GC-MS and HPLC-MS).  Examples of analytical instruments include mass spectrometers, chromatographs (e.g. GC and HPLC), titrators, pectrometers (e.g. AAS, X-ray, and fluorescence), particle size analyzers, rheometers, elemental analyzers (e.g. salt analyzers, CHN analyzers), thermal analyzers.

  • Track 22-1 LC-MS based nontargeted metabolomics
  • Track 22-2 Analytical instruments for nanomaterial characterization
  • Track 22-3 New trends in the analytical determination of emerging contaminants
  • Track 22-4 Lab-on-a-Chip device applications
  • Track 22-5 Preparation automation for GC injection
  • Track 22-6 NMR analysis of complex natural samples
  • Track 22-7 Analytical and preparative instrumentation

Liquid chromatography-mass spectrum analysis may be a key analytical technique that mixes the physical division capacities of liquid movement with the mass spectrometry examination abilities of spectrometry analysis. LC-MS framework is used for quick and mass coordinated filtration of characteristic items separates and new atomic substances important to nourishment, pharmaceutical, agrochemical and differing ventures. LC-MS is once in a while utilized as a part of medication advancement which we look at extensive variety of stages like, polluting influence recognizable proof, quantitative Bio-Analysis, and control. FDA has impelled testing of current quality testing of conventional solutions among prescription patients all through medication headway. Conventional Chinese Medicine is a recuperating framework created in China over 2,200 years back, consolidating medications that are now and again. One of its coordinating gauges is to dissipate malevolence and bolster the great Not withstanding treating disease, Traditional Chinese Medicine focuses on strengthening the body's safeguards and improving its capacity for recuperating herbs and to look after wellbeing.

  • Track 23-1 Current quality and regulatory issues associated with traditional medicines
  • Track 23-2 Overview of LC-MS bioanalysis related regulations
  • Track 23-3 Regulatory issues associated with traditional chinese medicine