Events

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

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

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

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 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

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

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

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

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

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 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

Join us at the Victoria and Albert Museum (V&A) for an afternoon with heritage scientists who work at the frontier of science and art, examining, analysing and preserving museum objects for future generations.
As part of the work championed by the

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 provides practical knowledge and hands-on experience of the technique of Fourier Transform InfraRed (FTIR) spectroscopy.

The course looks at the different components of FTIR and factors affecting spectral quality and mixtures. You will lea

Ensuring the quality of analytical data is a vital aspect of the work of an analytical scientist.
The effective planning of experiments and evaluation of data requires an understanding
of statistics. Knowledge of statistics is also needed to carry out

This one-day course provides practical knowledge and hands-on experience of the technique of UV-Vis spectroscopy covering method creation, sample analysis and data analysis. The course looks at the various applications of the technique and some of th

This one-day course looks at the technique of Atomic Absorption Spectroscopy (AAS) from the intial choice of analytical set-up; through to method development including sample preparation and sample introduction; through to calibration.

The course look

The Qualified Person must understand the influence of manufacturing pathways and associated physical and physico chemical attributes of both active pharmaceutical ingredients and major excipients on the quality of the finished dosage form.

QP respons

This one-day course will teach you about all stages of method validation from initial planning through to on-going tracking of performance statistics.

The course will include explanations of each important facet, initial data reduction, design of co

Thursday 6th February 2020
In silico techniques
Royal Society of Chemistry, London

As the pace of pharmaceutical development accelerates, and organisations look to reduce timelines in all parts of the discovery and development process, opportunities eme