Events

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 and interactive online training course provides the essential and practical theory about all available HPLC & LC-MS techniques.

This course has been approved by the Royal Society of Chemistry for purposes of Continuing Professional Developme

This course provides an introduction to Thermal Gravimetric Analysis (TGA), aimed at complete beginners. The course is also ideal for analysts or technicians looking for a refresher in these techniques.

This course explains the principles of these tec

The Government Chemist conference, ‘Safe food for tomorrow’s world’ will take place online on 23 and 24 June 2021. Full details here.

This conference was originally scheduled to take place in June 2020 and was postponed to June 2021 as a consequence

This course provides an introduction to the requirements of internal auditing described in the international standard ISO 19011. Frequent opportunities to practice key steps are provided through role play in a no risk environment, with supportive fee

The Qualified Person relies on the Pharmaceutical Quality System (PQS) to be able to fulfil their legal and operational responsibilities. This course provides a comprehensive overview of the requirements of the UK Study Guide. Scenarios and exercise

This live, instructor-led training course introduces the Agilent MassHunter software for instrument control, data acquisition and data analysis focusing on single quadrupole ICP-MS.

The course covers PC and data system set-up and maintenance; an overv

This live online training course provides an introduction to chemometrics for complete beginners.

This course also provides an overview of the history, development and current use of chemometrics in fields such as clinical, environmental, flavour and

The field of biologically derived medicines is expanding. With an increasing number of products being marketed, biological products bring unique challenges to the manufacturing process.

Biological products have unique challenges and constraints as co

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

A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.

Chemistry is ess

A refresher course in Chemistry, applied to the QC Laboratory environment, for pharmaceutical professionals and trainee QPs who haven’t studied Chemistry beyond GCSE level. Designed as a preface to the QP Analysis and Testing Module.

Chemistry is esse

Aseptic manufacturing

Steriles manufacturing remains one of the most challenging areas of the pharmaceutical industry from both a compliance and a technical perspective. The regulatory expectations continue to evolve, however slowly and new technology

This live and interactive Virtual Classroom training course provides an introduction to Mass Spectrometry Imaging, aimed at complete beginners. The course is also ideal for analysts or technicians looking for a refresher in the technique.

You will lea

This course covers the key concepts of Record and Data Integrity and Electronic Records and Signatures, including the key regulatory requirements and expectations (including Annex 11 and Part 11, and related guidance), example citations, and pragmat

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

This live and interactive online training course provides practical guidance to help you understand how to use the Automated Mass Spectral Deconvolution and Identification System (AMDIS) software to make the most of your analytical resolution to perf

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