Events

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

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 area of Advanced Therapy Medicinal Products (ATMPs) has expanded rapidly over the past few years and continues to expand at a fast rate. There are now a small number of products fully licensed, plus many more already undergoing clinical trials p

 The area of Advanced Therapy Medicinal Products (ATMPs) has expanded rapidly over the past few years and continues to expand at a fast rate. There are now a small number of products fully licensed, plus many more already undergoing clinical trials p

 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

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. This course

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. This course

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

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. 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

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