Events

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. This course

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

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. This course

Evaluation of data using statistical techniques is a key element of controlling the quality of pharmaceutical products for human and veterinary use. It is important to understand application of the data with which they will be presented. This course

 These online bitesize courses will provide an extensive and detailed introduction to Good Distribution Practices in the Pharmaceutical industry, covering best practices with practical examples.

For those who are new to Good Distribution Practice for

 The area of Advanced Therapy Medicinal Products (ATMPs) has expanded rapidly over the past few years and continues to expand at a fast rate. There are now a small number of products fully licensed, plus many more already undergoing clinical trials p

 The area of Advanced Therapy Medicinal Products (ATMPs) has expanded rapidly over the past few years and continues to expand at a fast rate. There are now a small number of products fully licensed, plus many more already undergoing clinical trials p

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

This live, instructor-led training course examines the method development process in detail; covering the objectives of the analytical method, how many components are to be separated and the required sensitivity, selectivity, specificity and the spee

This live, instructor-led training course introduces the Agilent MSD ChemStation software for instrument control, data acquisition and data analysis.

The course covers PC and data system installation, set-up and maintenance; an overview of MSD ChemSta

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

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

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 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 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

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

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

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

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

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