Events

This course is designed specifically as an introduction to the important topic of pharmaceutical microbiology. Intended for those seeking a clearer understanding of the topic and for Trainee QPs as a preface before attending our QP Pharmaceutical Mi

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 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

The course provides an overview of the concept of qualification and validation as described in Annex 15 to Eudralex Volume 4.

It covers responsibilities and terminology (qualification, validation and verification), and looks at the requirements of eq

The course provides an overview of the concept of qualification and validation as described in Annex 15 to Eudralex Volume 4.

It covers responsibilities and terminology (qualification, validation and verification), and looks at the requirements of eq

 These online bitesize courses will provide an extensive and detailed introduction to Good Distribution Practices in the Pharmaceutical industry, covering best practices with practical examples.

For those who are new to Good Distribution Practice for

The course covers facility/equipment qualification, process validation and validation of analytical methods. It covers regulatory guidance and requirements for Europe, US and elsewhere, including ICH.

This course is suitable for those working in most

This is a packed day that explores everything involved in becoming a Qualified Person (QP). Attendees are encouraged to ask as many questions as they like to ensure that you leave with a clear understanding and can make an informed decision whether

This is a practical based course. We explore the issues and pitfalls you may experience when performing Cleaning Validation. Help, guidance and training is given on techniques to overcome the issues in order to achieve a successful outcome.

After an i

This course is an adaptation of our standard 1-day GMP course, designed specifically for laboratory staff who have unique, additional requirements laid out in GMP both in the European and USA regulations and guidance documents.

The pharmaceutical qua

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

RSSL has been providing Responsible Person training since 2012. Our latest Cogent Gold Standard Approved online and classroom courses incorporate the very latest regulatory aspects, best practice, customer and industry input.

If your organisation alr

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

This course is designed specifically as an introduction to the important topic of pharmaceutical microbiology. Intended for those seeking a clearer understanding of the topic and for Trainee QPs as a preface before attending our QP Pharmaceutical Mi

COURSE overview 

Regulatory Inspections are a requirement in the Pharmaceutical industry and as people move on, sometimes the expertise on how to manage these is reduced or lost within specific organisations. In addition, new companies are regularly f

Regulatory Inspections are a requirement in the Pharmaceutical industry and as people move on, sometimes the expertise on how to manage these is reduced or lost within specific organisations. In addition, new companies are regularly finding themselve

Updated for 2020, this is a one day refresher course for Responsible Persons (RP) and Deputy RPs that have already attended their initial RP training.

Section 2.4 of Directive 2013/C 343/01 states that RPs should receive regular training to maintain

This course covers the key concepts of GxP computerised systems validation and compliance, including the key regulatory requirements and effective industry good practice based on GAMP®5.

Computerised systems validation and compliance is a basic GxP r

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