If you have a group of people requiring training, it may be more cost-effective for RQA to bring the training course to you.
Many of the standard professional development courses offered by RQA are available as in-house courses. We can also look into customising these courses to suit your organisation’s training objectives.
Some of the introductory courses have been successfully used by companies offering refresher training to their employees.
To find out how cost-effective in-house training can be, email us at email@example.com to discuss your requirements or complete our online quote request.Get A Quote
Cost saving – the cost per delegate is typically less when compared to sending the same number to public training courses.
Travel – no need for employees to travel any further than their offices and incur extra costs.
More specific – running a course for a single client could allow the training to focus on specific items that are causing issues within the business.
Convenience – fit around the working schedule of the staff and at a location they come to every day.
Membership – non-members can apply for free RQA membership after their attendance on the course.
Team building – a room full of delegates from different departments can encourage greater team work, awareness and understanding of each other’s roles.
Course tutors are active quality professionals in research and development.
Our standard courses are all CPD accredited.
|Advance Auditing Skills: Audit Analysis and Reporting||2 Days|
|Advanced Auditing Skills: Audit Planning and Performance||1.5 Days|
|An Introduction to Good Clinical Laboratory Practice (GCLP)||1 Day|
|An Introduction to Good Clinical Practice (GCP)||1 Day|
|An Introduction to Good Distribution Practice (GDP)||1 Day|
|An Introduction to Good Laboratory Practice (GLP)||1 Day|
|An Introduction to Good Manufacturing Practice (GMP)||1 Day|
|Audit Programmes and Risk Assessment||1 Day|
|Data Integrity for Auditors and QA||1 Day|
|Good Clinical Practice (GCP) Auditing - Principles and Practice||2.5 Days|
|Good Clinical Practice (GCP) Regulatory Inspections||2 Days|
|Good Laboratory Practice (GLP) for Study Directors, Principal Investigators, Study Staff and Management||2 Days|
|Good Laboratory Practice (GLP) Refresher||1 Day|
|Good Manufacturing Practice (GMP) for Investigational Medicinal Products||2 Days|
|Good Manufacturing Practice (GMP) in Pharmaceutical Laboratories||1 Day|
|ICH E6 Review & Update||1 Day|
|Implementing Good Clinical Laboratory Practice (GCLP)||2 Days|
|Managing Multi-site Good Laboratory Practice (GLP) Studies||1 Day|
Practical Application of Quality Risk Management (QRM) Tools and Techniques
|Practical Approach to Auditing Systems and Processes||2 Days|
Practical Pharmacovigilance Auditing
|QA Statistics Design & Analysis||1 Day|
Quality Systems for Research Laboratories
|Research Quality Assurance for Good Laboratory Practice (GLP)||2 Days|
Systems Approach to Good Pharmacovigilance Practice (GPvP)
The Auditing Course
Other courses or variants of these courses may be available.
If you are interested in onsite training for your team please contact us to discuss your requirements:
Telephone: +44 (0)1473 221411Get A Quote