Failure to meet GMP/cGMP, Data Integrity, Electronic Records, GDP requirements may lead to warnings, suspension, or withdrawal of license by regulatory institutions and could potentially cause health risks to your patients.

Within PiQuP AG lies an in-depth knowledge of cGMP requirements that is supported by turnkey expertise in Qualification and Validation.

In addition to providing all your documentation needs we can also develop qualification strategy, issue project schedule, actively coordinate and execute tests, and support you during inspections. Doing not enough or doing too much can lead to failure of the project, let’s work together in order to avoid redundancies and optimize your qualification and validation processes.

Qualification in Pharma and Medical Device Industry