Events

This live, instructor-led course looks at the technique of Inductively-Coupled Plasma Optical Emission Spectroscopy (ICP-OES); from the initial choice of analytical set-up through to designing a robust methodology, including sample preparation and sa

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 live instructor-led training course provides an introduction for complete beginners to Gas Chromatography (GC) and Gas-Chromatography-Mass Spectrometry (GC-MS), explaining the principles of these techniques, along with some of the industries whi

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

This live instructor-led training course is a pragmatic and practical guide to the process of investigating atypical and out-of-specification results in a GMP-compliant laboratory.

The course covers how to systematically investigate Out of Specificati

This live instructor-led 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 fragme

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

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 ou

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 live, instructor-led course provides an introduction to Ion Chromatography (IC), aimed at beginners. It is also ideal for analysts or technicians looking for a refresher in this technique.

This course explains the principles and limitations of th

This live instructor-led training course provides the essential and practical theory about all available GC & GC-MS techniques, covering how to select and use the GC carrier gas; sample introduction techniques; how to select a GC column, GC detector

This course provides a comprehensive introduction to liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS), aimed at complete beginners. The course is also ideal for analysts or technicians looking for a refresher in these

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

Whenever a measurement is made there will always be some uncertainty about the result due to unavoidable errors in the measurement process. Knowledge of this uncertainty allows a judgement to be made as to whether the data are likely to be ‘fit for p

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

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 ISO 15189 laboratory accreditation standards and m