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3rd European QA Conference 2019

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RQA's Pre-Conference Training Courses

The RQA is committed to providing valuable learning opportunities to enhance your professional development. We have selected four events for delegates to choose from and conference delegates receive a 10% discount on course fees using the code PRECON.

All events will be held at the Gibson Hotel, Dublin.

Course: The Auditing Course
4th - 5th November

One of our most popular courses, this course is specifically designed to develop and refine personal skills in the planning, performance and reporting of audits.

Applies to all types of audit and applicable to any area of regulated research and development. It is particularly valuable where there is a quality system requirement for audit. In order to gain maximum benefit from the course it is recommended that participants have personal experience of audit.

"Can't fault it at all!! All excellent speakers, really engaging and encouraging. Very easy to understand and remain attentive."

 

More information
(remember to use the code PRECON if booking with the 3rd EU QA Conference)


Course: Implementing Good Clinical Laboratory Practice
4th - 5th November

This course is designed to provide comprehensive guidance and practical help for those who are implementing Good Clinical Laboratory Practice (GCLP) in laboratories which undertake the analysis of samples from clinical trials. The course will address the current regulatory framework for laboratory work in support of clinical trials with reference to the ICH Guideline for Good Clinical Practice, the Clinical EU Trials Directive and related regulations and guidance. The course will also draw on the RQA guidance document on Good Clinical Laboratory Practice (GCLP).

"Good presentations, clear and helpful."

 

More information
(remember to use the code PRECON if booking with the 3rd EU QA Conference)


Course: A Masterclass in Pharmacovigilance Auditing
4th - 5th November

A new two-day masterclass, based on RQAs well established three-day Practical Pharmacovigilance Auditing course, will explore key phases of pharmacovigilance auditing. It will address the impact of the EU pharmacovigilance legislation on auditing and provide guidance on auditing pharmacovigilance systems at both the global and local organisational level. This course is designed for pharmacovigilance auditors, auditors new to pharmacovigilance and pharmacovigilance professionals to provide them with insight into developing and/or optimising a pharmacovigilance audit programme. In order to gain maximum benefit from the course, an understanding of pharmacovigilance is advantageous.

More information
(remember to use the code PRECON if booking with the 3rd EU QA Conference)


Seminar: Manageable Risk: Focusing on what Matters in Clinical Trials
5th November

This interactive one day seminar will share real life experiences and examples of what works.  One size does not fit all and this is your opportunity to access ideas and approaches to Clinical Trial risk management. Participants will get practical solutions and tools to enable support of their organisations in identifying, managing, mitigating and ultimately reducing the risks associated with clinical trials.

More information
(remember to use the code PRECON if booking with the 3rd EU QA Conference)

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