Continuous Process Verification is an age-old concept and industries such as Oil/Gas have been practicing it since the 70s, it is still a relatively new concept in Pharma with great potential to improve the manufacturing efficiency and quality. While the efficiency may be realized in the long term, the CPV is well poised to significantly increase the burden of compliance in the short term by reducing the number of required analytical testing.

So how can the number of required analytical samples be reduced to an optimum level? Read through the attached Micro Article to find out.