Events

This course provides an introduction to the requirements of internal auditing described in the international standard ISO 19011. Frequent opportunities to practice key steps are provided through role play in a no risk environment, with supportive fee

The field of biologically derived medicines is expanding. With an increasing number of products being marketed, biological products bring unique challenges to the manufacturing process.

Biological products have unique challenges and constraints as co

Run in partnership with Environmental Monitoring & Process Validation Specialists, Cherwell Laboratories, the course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products.

It looks at the legislation and gui

Successful completion of this one day course provides the delegate with understanding of the principles of Quality Risk Management (QRM) and its practical application.

The course is focused on ICH Q9 (QRM) and its support to ICH Q8 (Pharmaceutical De

This 5 day fully residential course provides the most comprehensive certification for Lead Auditors in the Pharmaceutical industry. Fully accredited by IRCA and PQG, this is a highly customised Lead Auditor Training course that has been specifically

Updated for 2021 in order to gain RSC Approval, this 3 day course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA.

This interactive course examines why we have Good Manufacturing Practice (GMP), its legal status and the key GMP issues surrounding pharmaceutical manufacture such as documentation, training and facilities. This informative course introduces the EU G

This interactive course examines why we have Good Manufacturing Practice (GMP), its legal status and the key GMP issues surrounding pharmaceutical manufacture such as documentation, training and facilities. This informative course introduces the EU G

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 service

This course provides an introduction to the requirements of systematic failure investigation (FI) and corrective and preventive action (CAPA) practices as described in ICH Q9 and made a regulatory requirement in Europe by Annex 20 of the Guide to GMP

The QP needs to understand the quality issues associated with the manufacture of biopharmaceuticals. Other modules in the RSSL QP Training Programme are based around the Study Guide, and therefore cover biotechnology products alongside other product

The QP needs to fully understand the challenges and risks involved in packaging operations in the Pharmaceutical Industry. A significant percentage of all product related complaints and recalls continue to be related to packaging issues. This course