Pharmaceutical Drug Analysis Training

pharma production training
  • Api (Active Pharmaceutical Ingredient)
  • Tablet
  • Pill
  • Capsule
  • Syrup, Dry Syrup
  • Parenteral
  • Cream
  • Lotion
  • Injection
  • Pharmaceutical Drug Analysis base on pharmacopeia like USP, BP, IP, EP & Other
  • Solution Preparation
  • Mobile Phase Preparation
  • Data Analysis, Generation
  • Data Verification
  • Calculation

K Laboratory provides an advanced methodology to detect drugs, advanced techniques of Drug testing. These techniques are being used by various professionals in the Pharmaceutical field for the detection of drug hence by getting trained under the guidance of our experts you will be able to get the job in the field of drug testing.

Modern Pharmaceutical Drug Analysis essentially involves as a necessary integral component even greater horizons than the actual prevalent critical analysis of not only the active pharmaceutical substances but also the secondary pharmaceutical products, the dosage forms having either single or multi-component formulated product. The fundamental reasons for this sudden legitimate surge in the newer evolving methodologies in the ‘analysis of drug substances’ are perhaps due to the tremendous growth in the progress of ‘medicinal chemistry’ towards achieving one ultimate objective which is to obtain ‘better drugs for a better world’. With the advent of computer-aided-drug modeling (CADM) the critical, scientific and faster approach to newer drug entities based on the biologically active prototypes, combinatorial chemistry, chiral chemistry and biotechnology has paved the way towards more specific, potent and above all less toxic ‘drugs’ to improve the ultimate quality of life in humans. Keeping in view the above astronomical growth in the design of complicated, specific and highly active drug molecules an equally viable, rigorous, accurate and precise analytical methods have been evolved with the passage of time which have now occupied pivotal and vital positions in most of the Official Compendia viz., USP, BP, EP, IP etc., for the analysis of such compounds both in pure and dosage forms.

The development of the pharmaceuticals brought a revolution in human health. These pharmaceuticals would serve their intent only if they are free from impurities and are administered in an appropriate amount. To make drugs serve their purpose various chemical and instrumental methods were developed at regular intervals which are involved in the estimation of drugs. These pharmaceuticals may develop impurities at various stages of their development, transportation and storage which makes the pharmaceutical risky to be administered thus they must be detected and quantitated. For this analytical instrumentation and methods play an important role. This review highlights the role of the analytical instrumentation and the analytical methods in assessing the quality of the drugs. The review highlights a variety of analytical techniques such as titrimetric, chromatographic, spectroscopic, electrophoretic, and electrochemical and their corresponding methods that have been applied in the analysis of pharmaceuticals.

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