All QPs need to understand the different Good Manufacturing Practice (GMP) requirements for commercial and Investigational Medicinal Products (IMPs), and the unique additional GMP requirements for IMPs. This two day interactive course examines the E

Further statistical tools for analytical scientists

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

Updated and revised for 2020, this intensive course provides an extensive and detailed introduction to Good Distribution Practices in the Pharmaceutical industry. Covering best practices with practical examples and an overview of the regulatory fram

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

Compliance with the forthcoming Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare for these challenges and transition sm

Compliance with the forthcoming Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare for these challenges and transition sm

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

This course provides the knowledge and skills to enable effective auditing and reporting of audits on suppliers of active pharmaceutical ingredients (APIs). The course is focused on the requirements of ICH Q7 and EU GMP Part II and the expectations

 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 Analytical Research Forum (ARF) provides the opportunity for early career researchers from analytical communities to present their work, alongside high profile analytical scientists. This flagship event of the Analytical Division will showcase cu

Overview: 

This webinar will cover the following themes:
· What are the key challenges to achieving Net-Zero by 2030 in the UK water sector ?
· Look at the key levers which will allow us to succeed.
· How can sensors optimise processes and systems to d

This is a packed day that explores everything involved in becoming a Qualified Person (QP). Attendees are encouraged to ask as many questions as they like to ensure that you leave with a clear understanding and can make an informed decision whether

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 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

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

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

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