Call for Abstract

2nd International Conference on Pharmaceutical Analysis
Analytical Chemistry
, will be organized around the theme “New paradigms in Pharmaceutical Analytical Techniques”

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

Submit your abstract to any of the mentioned tracks.

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

Generally, Pharmaceutical Analysis alluded to the synthetic examination of medication atoms. Be that as it may, throughout the years, present day pharmaceutical investigation has advanced past this to envelop mix systems, high-throughput innovations, chemo metrics, micro dosing studies, scaling down and nanotechnology. These logical advances are currently being utilized in all phases of medication disclosure and the concentration of this survey will be on how these advances are being utilized inside this procedure. With new, enhanced and advancing innovations, and in addition new applications for existing innovation, the scan for new medications for the aversion and treatment of human maladies proceeds.



  • Track 1-1Solid State Analysis
  • Track 1-2Phytopharmaceutical Analysis
  • Track 1-3Novel Dosage form Analysis
  • Track 1-4Electrically Driven Analytical Methods
  • Track 1-5SFC and NMR Spectroscopy
  • Track 1-6Building Bio betters: The regulatory landscape
  • Track 1-7Total Quality Management

Chromatography strategy for isolating the parts, or solutes, of a blend on the premise of the relative measures of every solute appropriated between a moving liquid streams, called the versatile stage, and a touching stationary stage. The versatile stage might be either a fluid or a gas, while the stationary stage is either a strong or a liquid. Increase in advances in Biotechnology sector augments the production of variety of valuable bio products. Molecules such as therapeutic proteins, enzymes, and other important products require combination of chromatography so as to purify them in purest form. Combination of these novel technologies minimizing the purification steps plays a crucial role for getting maximum purification of the biomolecules.



  • Track 2-1Partition Chromatography
  • Track 2-2Ion exchange Chromatography
  • Track 2-3Affinity Chromatography
  • Track 2-4Gas Chromatography
  • Track 2-5Special Techniques in Chromatography
  • Track 2-6Advancements and Applications in Chromatography
  • Track 2-7Novel Techniques in Chromatography
  • Track 2-8Separation Techniques in Chemistry

Analytic method development and validation are persistent and interconnected exercises directed all through the drug development process. The act of validation checks that a given method measures a parameter as planned and sets up the execution furthest reaches of the estimation. Albeit clearly conflicting, approved methods create comes about inside known vulnerabilities. These outcomes are essential to proceeding with drug development, as they characterize the rising learning base supporting the product. The time and exertion that are put into growing logically solid, hearty, and transferrable analytic methods ought to be lined up with the drug development arrange. The assets that are consumed on method validation must be constantly balanced with regulatory requirements and the likelihood for product commercialization.



  • Track 3-1Method Development
  • Track 3-2Optimization
  • Track 3-3Method Transfer and Revalidation
  • Track 3-4System Suitability

Spectroscopy deals with surplus of different techniques that employ electromagnetic radiation on materials in order to measure and interpret data, which is used for elucidating a variety of analytical problems. It includes absorption, emission, or scattering of electromagnetic radiation by atoms or molecules. Types of spectroscopy are IR & NIR, UV/visible, NMR, Atomic Emission Spectroscopy, Fluorescence Spectroscopy etc. Spectroscopic methods are used for Environmental Analysis, Biomedical studies, astronomy. UV-Visible Spectrometer is used for a varied range of applications.


  • Track 4-1High Performance Liquid Chromatography
  • Track 4-2Fourier Transformation Infrared Spectroscopy
  • Track 4-3Ultraviolet/Visible Spectroscopy
  • Track 4-4Recent advances and developments in spectroscopy
  • Track 4-5Applications of Spectroscopy

Analytical biochemistry is the study of biochemical components found in a cell or other biological sample. This field uses a broad vary of techniques for separation, identification, quantification and practical characterization of biological molecules like nucleic acids, enzymes, proteins, pigments, carbohydrates and additional. The main ways involved in analytical biochemistry to separate the biological components are qualitative analysis techniques, chromate graphical Techniques, super molecule Estimation & Purification Techniques and medicine Techniques.



  • Track 5-1Membrane technology in separation processes
  • Track 5-2Novel separation techniques in chemistry
  • Track 5-3Emerging Separation Technologies
  • Track 5-4 Biological techniques

New mass spectrometry (MS) methods, collectively known as data independent analysis and hyper reaction monitoring. Last decade has witnessed remarkable technological advances in mass spectrometry based proteomics and Biologics. Specific advances include high throughput protein identification by multidimensional chromatography, automated tandem mass spectrometry and sequence data base searching, accurate quantification by the application of stable isotope dilution theory to protein analysis, and the targeted isolation of selected analytes by the use of highly selective chemistries.


  • Track 6-1Mass Spectroscopy in Proteomics
  • Track 6-2Applications of Mass spectroscopy in Food science
  • Track 6-3Ionization Techniques in Mass Spectroscopy
  • Track 6-4Imaging Mass Spectrometry
  • Track 6-5Mass spectrometry in Environmental analysis
  • Track 6-6Clinical Applications of Mass spectrometry

Bioanalysis involves 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. In the past two decades, has seen increase in the field of Biopharmaceuticals. Bioanalysis applies to the drugs used for anti-doping testing in sports, illicit purposes and Environmental concerns. The most frequently used techniques are liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for micro molecules and enzyme-linked immunosorbent assay (ELISA) for macromolecules.


  • Track 7-1Dual polarization interferometry
  • Track 7-2ELISA (Enzyme-linked immunosorbent assay)
  • Track 7-3MIA (magnetic immunoassay)
  • Track 7-4RIA (radioimmunoassay)
  • Track 7-5Solid phase extraction

Electrochemical Analysis is a powerful technique that is increasing in utility in the Pharmaceutical Industry due to its high sensitivity, speed of analysis, reduction in solvent and sample consumption, and low operating cost compared to other analytical methods. The modern Electrochemical Analytical techniques are cyclic, linear sweep, differential pulse, square wave and stripping voltammetric techniques. Thermo Analytical techniques are mainly used to detect compound purity, polymorphism, solvation, degradation, and excipient compatibility. It is extensively used in conducting Preformulation studies.


  • Track 8-1Coulometry
  • Track 8-2Voltammetry
  • Track 8-3Differential Scanning Calorimetry
  • Track 8-4Differential Thermal Analysis
  • Track 8-5Thermo Gravimetry

Analytical Chemistry has many applications in Forensic Sciences, environmental analysis, and materials analysis. Analytical Chemistry research is mainly driven by the performance and cost. In these days, great efforts are being put to shrinken the analytical techniques to chip size. In this technology, the most used technique is lab-on-a-chip. The ongoing developments of computer automation and information technologies have broadened the analytical chemistry into a number of new biological fields.



  • Track 9-1Qualitative analysis
  • Track 9-2Quantitative analysis
  • Track 9-3DNA Analysis
  • Track 9-4Microscale chemistry
  • Track 9-5Green Chemistry

Preformulation is considered as critical decision-making tool during both – drug discovery and development phase. Preformulation studies help in assessing the drugability of a molecule. To generate Preformulation data analytical techniques like Spectroscopic, Chromatographic, Thermal methods and some specific detection methods like Capillary electrophoresis are used.


  • Track 10-1Analytical techniques and Instruments for Preformulation Studies
  • Track 10-2Thermal Analytical Methods
  • Track 10-3Separation sciences
  • Track 10-4Specific Detection

Hyphenated technique is developed from the coupling of a separation technique and an on-line spectroscopic detection technology. These techniques are mainly broadened their applications  in  the analysis  of natural products.



  • Track 11-1LC-MS
  • Track 11-2GC-MS
  • Track 11-3LC-FTIR
  • Track 11-4LC-NMR
  • Track 11-5CE-MS

Quality assurance is defined as a procedure or set of procedures intended to ensure that a product or service under development meets specified requirements. Quality control (QC) is a procedure or set of procedures intended to ensure that a manufactured product or performed service adheres to a defined set of quality criteria that meets the requirements of the client or customer. The two approaches can be thought of simply as failure detection (QC) and failure prevention (QA). The ISO 9000 family of quality management systems standards is designed to help organizations ensure that they meet the needs of customers and other stakeholders while meeting statutory and regulatory requirements related to a product or service.


  • Track 12-1Quality by Design
  • Track 12-2Quality risk management
  • Track 12-3Good Manufacturing Practice

Analytical errors are fundamental before submitting your report and results with the required level of confidence. However, we should have clarity regarding accuracy and precision before we are talking pharmaceutical error. Most of us believe that these terms have the same meaning but the example of arrows striking a target. Any measurement is limited by the precision of the measuring instruments and the technique and the skill of the observer. Where a measurement consists of a single reading on a simple piece of laboratory equipment, for example, a burette or a thermometer, one would expect the quantity of factors adding to vulnerabilities in that estimation to be less than an estimation which is the consequence of a multi-step process comprising of at least two weight estimations, a titration and the utilization of an variety of reagents.


  • Track 13-1Determinate errors
  • Track 13-2Indeterminate errors
  • Track 13-3Statistical treatment of finite samples
  • Track 13-4Sampling statistics

Good manufacturing practice is the piece of quality assurance which ensures that things are reliably made and controlled to the quality standard proper to their proposed use and as required by the Marketing Authorization or item particular. GMP is stressed over both generation and quality control, consistency with this standard gives open assurance that the rights, security, and prosperity of trial subjects are ensured; predictable with the rule that have their starting point in the Declaration of Helsinki, and that the clinical information is valid.


  • Track 14-1Guideline versions
  • Track 14-2High-Level Details
  • Track 14-3CGMP inspections
  • Track 14-4Enforcement
  • Track 14-5Controlled Environmental conditions

Biosensor is a device which converts the information regarding the presence of a compound into electro analytical Signal. The biosensor research areas include modern Bio specific analytical techniques. In the recent years, micro fabrication techniques have showed a significant improvement in biosensor systems. The modern methods of the biosensor discoveries range from electrochemical, electromechanical, and fluorescence-­cum-optical-based biosensors and genetically engineered microbes.


  • Track 15-1Nanomaterial based Biosensors
  • Track 15-2Optical Biosensors
  • Track 15-3Ultrasensitive Biosensors
  • Track 15-4Materials used in Biosensors
  • Track 15-5Genetically encoded Biosensors
  • Track 16-1Gas ionization detectors
  • Track 16-2Gamma Spectroscopy
  • Track 16-3Radionuclides
  • Track 16-4Radioanalytical Techniques

Multiply hyphenated techniques, such as gas chromatography/ mass spectrometry with retention time locking (GC/MS/RTL), liquid chromatography/time-of-flight mass spectrometry (LC/ MS/TOF), micro fluidic-based capillary electrophoretic analysis of mitochondrial DNA (mtDNA), and laser ablation inductively coupled plasma mass spectrometry (LA/ICP/MS), are able to uncover forensically germane information by providing unprecedented levels of analytical selectivity and sensitivity


  • Track 17-1Forensic Laboratories
  • Track 17-2Trace evidence
  • Track 17-3Forensic Chemistry

Modern microbiology is unmistakably a branch of biotechnology and incorporates the customary and nucleic corrosive aspects. Pharmaceutical microbiology is the connected branch of microbiology which enables drug specialists to make pharmaceuticals from microorganisms either straightforwardly or with the utilization of some item delivered by them.  Different parts of pharmaceutical microbiology incorporate innovative work for assembling of different hostile to tumours, against microbial specialists.


  • Track 18-1Validation of Disinfectants
  • Track 18-2Antimicrobial activity and Disinfection
  • Track 18-3Sterile Products
  • Track 18-4Exotoxin and Endotoxin