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 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

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 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

SWIG/KTN SENSOR SPRINT

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

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

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

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

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 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

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

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