Our training courses combine lectures with workshops and role play to ensure that theoretical information can be applied in practice. Training courses include GCP from beginner to advanced; preparation for and hosting of regulatory inspections; GVP regulatory updates; conducting quality audits. Course materials are provided and all delegates receive a Certificate of Attendance.


Comprehensive GCP training


Inspection readiness training


Conducting regulatory audits

Find out how ADAMAS Consulting can help with your next project

Recent examples of our work:

Comprehensive three-day training course on GCP regulations and guidelines.

One-day training course conducted in parallel in UK and US on GCP and common inspection findings.

Japanese GCP training provided with simultaneous translation

ADAMAS Consulting provides bespoke, tailored training courses to meet client’s specific needs in the areas of:

  • Computer System Validation
  • Clinical Quality Assurance
  • European and US Clinical Trial Regulations
  • Regulatory inspection readiness

The training courses combine lectures with workshops to ensure that theoretical information can be applied in practice. Course manuals are provided as reference material, and all delegates receive a Certificate of Attendance.

On behalf of the team I would like to thank you for the training; the input already triggered and serves as direction for a gap-analysis meeting we will arrange very soon.


Q.A. Director, European CRO

Contact Us

If you've got any questions or queries about our services, careers, or training, please get in touch.
We have 500+ years combined experience, working around the globe there isn’t anything we’ve not encountered in our sector. We're very approachable and happy to help.

Contact Adamas
The ADAMAS Corporate Brochure 2016


Brochure – Please download the ADAMAS brochure describing our QA services and contact details.

Regulatory Environment


The development of medicines is the most regulated industry in the world, and compliance at each stage of the research and development process, as well as after licensing, is critical to ensuring high quality and safe medicines reach patients in a timely manner.



ADAMAS’s consultants have expertise across the G’X’Ps in pre-clinical, clinical and post-licensing areas. They have worked across many different therapeutic areas and product types including oncology, vaccines, biologics, medical devices and gene therapy. As a company we have developed close partnerships with our clients to support them in their development programmes and post-licensing activities, and to guide them successfully through their worldwide regulatory inspections.


How to be a Clinical Auditor


‘So you want to be a Clinical Auditor?’, an article written by CEO Dr. Patricia Fitzgerald.

Benchmarking Data


Please download our benchmarking data sheet, to see how these data compare with your own performance. To discuss a more detailed report, or analysis of a data subset, please get in touch.

Is your QMS compliant?


Is your QMS compliant to the upcoming ICH E6 Addendum? Download our 5-point checklist

ICH (E6) R2 Addendum - Step 4


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