It is a regulatory requirement for organisations within the Pharmaceutical and Allied Industries to audit active pharmaceutical ingredient (API) manufacturers, suppliers of key excipients and packaging materials, and contracted-out laboratory services. This course is aimed at reviewing the key relevant standards that one might expect to audit against, providing a strong foundation for the application of auditing skills. Specifically this course covers the EU GMP Parts I, II and III; PS 9000; ISO 17025; ISO 15378 and ISO 13485. Several elements of ISO 9001 (Quality Management Systems) are explored in detail.
Who Should Attend
The course is suitable for all those who need an appreciation of the above standards in order to audit within the pharmaceutical industry and allied industries, particularly those who undertake external supplier audits. In addition to those with a dedicated auditing role, it is also suitable for Qualified Person鈥檚 (QP).
Who Should Attend
The course is suitable for all those who need an appreciation of the above standards in order to audit within the pharmaceutical industry and allied industries, particularly those who undertake external supplier audits. In addition to those with a dedicated auditing role, it is also suitable for Qualified Person鈥檚 (QP).
