Pharmaceutical analytical testing refers to the use of scientific techniques and methods to establish the identity, strength, quality, purity, and potency of drug products. It plays a crucial role in drug development and manufacturing processes to ensure patient safety. Analytical testing helps characterize drug substances, finished drug products, intermediates, ingredients in a drug product, and degradation products. It also aids in compound identification and quantification, purity analysis, dissolution or release testing, bioavailability or bioequivalence studies, and stability testing. The techniques used include chromatography, spectroscopy, titrimetry, and microscopy. With stringent regulatory norms and new drug approvals, the demand for quality control and analytical testing services from pharmaceutical and biotechnology companies is increasing significantly.
Market Dynamics:
The global pharmaceutical analytical testing market is driven by factors such as rising drug research and development activities, tighter quality control norms, and increased outsourcing of testing needs by pharmaceutical companies. Moreover, advancements in analytical techniques such as HPLC, GC, NMR, and MS/MS are enabling superior characterization of complex drug molecules and their metabolites, thereby accelerating the market growth. However, high costs associated with analytical instruments and lack of skilled professionals are hindering the market to a certain extent. Growing generic and biosimilar drug markets in emerging nations offer lucrative opportunities for market players. In addition, increasing collaborations between analytical testing service providers and pharmaceutical firms will boost market revenues during the forecast period.
Key Features of the Study:
Detailed Segmentation-
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*Browse 32 market data tables and 28 figures on "Pharmaceutical Analytical Testing Market” - Global forecast to 2031
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