The BMSS Introduction to Mass Spectrometry course covers all fundamental aspects of mass spectrometry, including theory, instrumentation, applications, interpretation and best practice.

Who should attend?

This introductory course assumes an undergra

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

Regulatory Hot Topics VI

This symposium will address issues and challenges associated with the implementation of new and emerging guidelines. It will provide an excellent opportunity for dialogue, discussion and debate with speakers - several of whom

This course provides an introduction to the requirements of systematic failure investigation (FI) and corrective and preventive action (CAPA) practices as described in ICH Q9 and made a regulatory requirement in Europe by Annex 20 of the Guide to GMP

It is a regulatory requirement for organisations within the Pharmaceutical and Allied Industries to audit active pharmaceutical ingredient (API) manufacturers, suppliers of key excipients and packaging materials, and contracted-out laboratory service

This live instructor-led training course provides an introduction to metabolomics for complete beginners.

The course provides an overview of the history, development and current use of metabolomics in fields such as clinical, environmental, flavour an

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

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

Registration is now open for the Stimulated Raman Scattering (SRS) Microscopy Workshop

Agenda coming soon.

Applications for contributed talks (15 mins including questions) or flash poster presentations (5 mins) are welcome, please submit your title a

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

Modern analytical instruments are capable of producing a large amount of data. To interpret this data effectively requires the application of statistics. This course builds on the topics covered in the ‘Statistics for analytical scientists’ course an

SWIG/KTN SENSOR SPRINT

This live, instructor-led course covers the theory of purge-and-trap (P&T) and how to modify samples to improve results, how to create P&T methods, analyse samples and the parameters that can be optimised.

Delegates will learn the individual steps and

Updated for 2021 in order to gain RSC Approval, this 3 day course systematically builds up the knowledge of delegates over three intensive days. It covers the regulations and guidelines associated with GMPs and the expectations of the MHRA and FDA.

This course covers all the essential theory about analytical derivatisation prior to sample analysis, along with the need and importance for better chromatography, sensitivity and stability.

The course will review the different types of derivatisation

On this live, instructor-led Virtual Classroom training course you will learn about UHPLC methods and why we need to migrate methods from HPLC to UHPLC.

The course will review the principles and limitations of HPLC and you will learn the reasons behin

This live, instructor-led online training course covers all the practical theory of Liquid-Liquid Extraction (LLE).

The course covers solvent extraction, partitioning, solubility, miscibility, sample preparation, matrix modification including pH adjus

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

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