Discovery and Development
 

 

GlobalPlus Diagnostics Laboratory will work with you on studies in all stages of drug development including programs in the discovery and development stage. We provide pharmaceutical impurity testing for new drug substances and new drug products which can support your product development from an early stage and across the lifecycle of your drug product. Impurity testing for pharmaceuticals is a necessary step in creating a quality product for the market.

Chemical impurity analysis is the scientific process of isolating unknown materials in chemicals, polymers, packaging, pharmaceuticals, finished products, in order to identify them.

There are typically three groups of impurities which are evaluated and identified when conducting impurity analysis:

  • Organic impurities
  • Inorganic impurities
  • Residual solvents 


As a full-service lab, GPD Laboratory scientists are experts at performing unknown material analyses and identifying any trace materials, residuals, or impurities in even the most difficult of sample matrices. We have extensive experience working with active pharmaceutical ingredients and drug product, across all major dosage forms and delivery systems.

Chemical impurity testing is incredibly important as impurities and irregularities can cause massive disruption for organisations through product recalls and delayed manufacturing timelines. Particularly in the medical industry, any impurities can have an impact on the company’s product and image. Do not leave your company’s reputation up to chance—GPD Laboratory will ensure there are no contaminants or impurities in your products.

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