Events

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

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 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 Mass Spectrometry Imaging, 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 techniques,

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

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

 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 course introduces the fundamental theory of triple quadrupoles for MS/MS, looks at the hardware and maintenance differences between the single quadrupole and triple quadrupole, before moving onto the MassHunter software for use with MS/MS includi

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

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

This course has been approved by the Royal Society of Chemistry (RSC) for purposes of Continuing Professional Development (CPD).

This live, instructor-led training course looks at method validation from start to finish; including explanations of each

This live instructor-led training course course teaches the strategies for HPLC & LC-MS method development, system optimisation and configuration, how to recognise areas requiring maintenance on the instrument and the logical steps of instrument trou

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

Run in partnership with Environmental Monitoring & Process Validation Specialists, Cherwell Laboratories, the course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products.

It looks at the legislation and gui

TITLE OF EVENT: The JPAG pharmaceutical analysis research awards 2021

EVENT LINK: https://www.jpag.org/161

WEB LINK: https://www.jpag.org/

CONTACT: Hon Events Secretary JPAG, events@jpag.org

SPEAKERS:
Prof David Cowan - King's College London

JPAG presents

Successful completion of this one day course provides the delegate with understanding of the principles of Quality Risk Management (QRM) and its practical application.

The course is focused on ICH Q9 (QRM) and its support to ICH Q8 (Pharmaceutical De

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 live, instructor-led online training course covers all the practical theory of Liquid-Liquid Extraction (LLE).

The course covers solvent extraction, partitioning, solubility, miscibility, sample preparation, matrix modification including pH adjus

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