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This live online training course provides an introduction to mass spectral interpretation, providing all the fundamental tools and rules when examining high quality full-scan GC-MS data.
The course teaches how to obtain high quality mass spectra, simp
This live, instructor-led training course covers all the essential theory about Solid Phase Extraction (SPE) as a means of sample preparation.
The course will review the different types of SPE processes used for sample extraction including non-polar S
On this live and interactive 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 training course looks at preparing for problems, how to identify problems and the troubleshooting process. This knowledge, along with the basic knowledge of HPLC & LC-MS acquired in the Practical Essentials of HPLC & LC-MS, a
This live, instructor-led online training course looks at the areas requiring maintenance on the instrument.
The course first looks at clean-up procedures for difficult samples. Then, the parts of the LC & MS system requiring maintenance, how often an
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
