For R5061 running on 3rd July 2024, we are offering a 20% discount (not to be used in conjunction with other offers) using R506120 in the discount code box at checkout.
This highly interactive course will provide guidance on why and how to implement a quality system successfully into the research laboratory. By doing so, you will position your innovation for the success it deserves. But leave things as they are and there is a good chance that your science will not realise its full potential should success, and its consequences, come your way.
A quality system in your research laboratory is the most effective and efficient way to:
This course is particularly aimed at those working in early phase research environments which are not constrained by the regulatory requirements of the Good Practice regulations but are producing intellectual property, testing and/or products for the therapeutic market. For organisational reasons, rather than regulatory ones, this is a place where you need to get it right.
The programme is delivered by leaders in the field who, quite simply, ‘have done it’. Whether delegates are at senior management level seeking strategic direction, a laboratory head wishing to deliver science that will stand the test of time or a quality professional thrown in at the deep end, this course will provide key insight and practical guidance to underpin future success. Based on risk based systems, tried and tested over many years in the workplace, the programme will help delegates to define, train, implement and monitor the quality of their research, irrespective of field or discipline. Delegates will learn how to help position their organisation for success.
Delegates will be guided thoughtfully through each key component of the process in a stimulating learning environment. The course probes all avenues of the research quality arena, from an initial understanding of the cultural aspects of the scientific discovery environment, to managing quality in outsourced research programmes. Computer systems and e-data security in the research environment will be discussed and pragmatic solutions described to help manage the ballooning cloud of e-data. In addition, the ever blurring boundary between the regulated and non-regulated research environments will be discussed and delegates given perspective on future developments in the field.
With this knowledge, delegates will be able to get it ‘right first time’.
The course is designed for all those involved in the research laboratory quality arena and it has been tailored to meet the needs of scientific management, bench scientists and quality professionals alike.
Delegates get immediate access to highly experienced tutors who will share their wisdom and insights in an area where few others have been successful. The course is linked with the RQA guidance which builds on years of experience and forms the foundation of the programme.
Tutors will be comprised of (click the photos for biographies):
After 15 years spent in Research, Sandrine joined the Quality Assurance field in 2012. Today, as Associate Director in Research and Quality Compliance at Novartis, in Basel, Switzerland, she develops, implements, and monitors holistic, risk based, non-GxP quality programs in research laboratories. She leads and support non-GxP, GLP and GcLP audits.
Sandrine is also actively involved in EU-funded projects aiming to enhance Quality Systems, Data Integrity, and Ethics in Research, such as EQIPD and BEYOND.
Please note timings may be subject to alteration.
Examples of business and regulatory risks and the consequences of low quality in research. A look at the standards and guidelines that exist.
Understanding research environments, the drivers, challenges and importance of culture change. How to change hearts and minds.
What's "required", nice to have, or can come later.
Thinking about risk management and prioritisation. Looking at the critical factors for the implementations of a successful quality system.
Considerations and risks in the lab.
Looking at planning the work, defining procedures in a way which promotes robust science without compromising brilliance and ensuring that all these elements are demonstrably fit for their intended purpose.
How much validation is required at what stage? What do we need to do to validate an assay?
Accurate, attributable, legally attestable and safe data and records of experiments and studies. Looking at practical aspects of the work where there is a chance to review, correct or improve the science, the data and the processes.
What to consider when working with collaborators and other labs.
Reviewing implementation of a quality system, finding opportunities for improvement, understanding culture change.
This course will be run completely online. You will receive an email with a link to our online system, which will house your licensed course materials and access to the remote event.
Please note this course will run in UK timezone.
You will need a stable internet connection, a microphone and a webcam.
7 Points
Develop
Guidelines for Quality in Non-Regulated Scientific Research eBooklet
Introduction to Quality Risk Management (QRM) elearning
Introduction to Risk Based Quality Systems (RBQS) elearning
Management of the Training and Competency of Personnel in GxP and Research Environments eBooklet
Quality in Research eBooklet
Quality Systems elearning
Webcast - Quality Systems