Events

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 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

This course is designed to provide a clear process for writing any report, with or without a template or required outline. The result is the ability to produce a better report and to make far better use of the time available.

The emphasis is on plann

This course provides an introduction to the fundamentals of LC-MS mass spectral interpretation.

The course teaches how to obtain high quality mass spectra, simple techniques to recognise and elucidate spectra, how to observe fragmentation patterns and

Evaluation of data using mathematical and statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use.

The Qualified Person must understand the derivation and application of the data with

Scope: Data from on-line instrumentation is increasingly being used for process optimisation and control and for monitoring compliance critical operations. Such instrumentation is therefore becoming fundamental for managing risk, maximising efficienc

Measurement uncertainty evaluation is a requirement for laboratories accredited to
ISO/IEC 17025. Whenever a measurement is made there will always be some uncertainty
about the result due to unavoidable errors in the measurement process. Knowledge of t

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 Mic

Learn all the essential theory of liquid chromatography and LC-MS along with hands-on practicals in the laboratory.

The course covers solvents & buffers (the mobile phase), pumps, isocratic and gradient elution, sample introduction, analytical columns

This course has been approved by the Royal Society of Chemistry for purposes of Continuing Professional Development (CPD).

Learn about and practice some advanced and powerful GC techniques which could be very useful for your analysis on this 2-day han

The Qualified Person should have a thorough knowledge of formulation and processing of the medicinal products they are asked to certify. This six-day (two part) module provides basic formulation principles, including preformulation studies, bioavaila

Gain hands-on experience of modern Liquid-Liquid Extraction (LLE) on this 1-day practical training course.

Learn about this sample preparation technique for GC (& GC-MS) and HPLC (& LC-MS) including real world applications.

Learn all the practical theo

This course covers the essential theory and chemistry behind analytical derivatisation for GC-MS or LC-MS. Learn about the dfferent types commonly used, how to select a suitable agent and gain hands-on experience in the process of derivatisation.

Lear

This 1-day course covers all the essential theory along with practical experience in Solid Phase Extraction (SPE) as a means of sample preparation.

The course looks at the different SPE processes and the advantages and disadvantages of each and the ty

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 course has been approved by the Royal Society of Chemistry for purposes of Continuing Professional Development (CPD).

This one day course teaches the theory along with practical experience on how to use Solid-Phase Micro-Extraction as an automate

Qualified Persons cannot fulfil their role in a responsible way unless they understand the actions and uses of the medicinal products manufactured and those they are asked to certify. This course provides further understanding of product ‘fit for its

This course has been approved by the Royal Society of Chemistry for purposes of Continuing Professional Development (CPD).

​Learn the theory and gain practical experience of how to use Headspace as an automated sample preparation technique for GC or G

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 ISO15189 laboratory accreditation standards and ma

This course has been approved by the Royal Society of Chemistry for purposes of Continuing Professional Development (CPD).

Learn the theory and gain practical experience of how to use Purge-and-Trap (P&T) as an automated sample preparation technique f