Qualification and validation are two essential concepts in the pharmaceutical industry that pursue a common goal: Ensuring the quality of medicinal products. While qualification concentrates on the suitability of equipment, validation focuses on proving the suitability of processes.
In both cases, it is crucial that predefined specifications are reliably fulfilled under consistent conditions. Comprehensive documentation is essential here, as it forms the basis for compliance with the standards - after all, “if it's not documented, it didn't happen”.
With our training courses, we support you in finding your way around the complex requirements of validation and qualification.
When you book selected seminars, we also provide you with the corresponding Standard Operation Procedures (SOPs). This additional material provides you with important regulations and requirements to optimize internal workflows and make them more efficient.
