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CPL|17 October 2018

Analytical Testing Services for Pharmaceutical Formulation Development

CPL's formulation development scientists work hand-in-hand with a team of analytical scientists during new product development and product transfers.

CPL’s formulation development scientists work hand-in-hand with a team of analytical scientists during new product development and product transfers.

The company offers a comprehensive range of testing services, ranging from research and development (R&D) to routine analytical testing, microbiological testing, in-vitro release testing (IVRT) and stability programme management.

CPL’s analytical methods and testing capabilities include:

  • Analytical method development and validation
  • Method transfers
  • Forced degradation studies
  • Cleaning method development and validation
  • Product problem investigations
  • Non good manufacturing process (GMP) and GMP-standard IVRT

The company’s stability management operations feature:

  • Six walk-in stability chambers that meet International Conference on Harmonisation (ICH) conditions
  • Dedicated stability coordinators
  • Remote alarm monitoring of chambers with backup generators

Isopropyl myristate (IPM) is widely used as a penetration enhancer and emollient in topical formulations.
Gas chromatography (GC) is a typical chromatographic method used to separate and quantitatively determine analytes that can be volatised without decomposition.
CPL develops and manufactures non-sterile liquid and semi-solid pharmaceutical products. We are solely focused on these dosage forms and have built our reputation as an...
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