Events

Method validation is the process that provides evidence that a test method is capable of producing results that are suitable for a particular application. It is a requirement of the ISO/IEC 17025 and ISO 15189 laboratory accreditation standards and m

A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.

Chemistry is ess

A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.

Chemistry is esse

Aseptic manufacturing

Steriles manufacturing remains one of the most challenging areas of the pharmaceutical industry from both a compliance and a technical perspective. The regulatory expectations continue to evolve, however slowly and new technology