TMQA Latest News


Our monthly Regulatory and Pharma News Update for February has been published and can be accessed at this address 

Highlights include:

  • HMA publishes guidance on Reference Safety Information;
  • MHRA opens consultation on exemptions to the Medical Device and In-vitro diagnostics regulations;
  • MHRA publishes advice on use of pharmacovigilance service providers;
  • EMA and MHRA provide guidance on preparation for Brexit;
  • Use of form FDA 1572 in trials in Europe;
  • FDA launches clinical trial transparency programme

Quality Assurance Training

TMQA is runn ing its popular Research Quality Assurance training course at its Edinburgh facility on 26th and 27th March.

This is a great chance to learn about audit and inspection from leading experts in the field. For further information please click on the `Read More` button below.

Read More »

TMQA Regulatory Update - January 2018

The January Edition of our popular Regulatory Update is now available:

  • EMA Management News
  • MHRA Clinical Stakeholders Engagement Meeting
  • Highlights from the ICH Assembly
  • TransCelerate publishes new eConsent Guidance and Tools

Dowload your copy here - January Regulatory Update

Operations Manager Appointed

Lianne Roeling has been acting Operations Manager since Adele McMeekin left in October. we are delighted that she hs now taken the position on a permanent basis.

Arrivals and Departures

TMQA is delighted to announce that Dr Eva Voros will join our Clinical team at the beginning of January. Eva is a Medical Doctor who has been working in clinical research for twenty years and has a qualification in clinical Quality Assurance. She will be part of our Central Europe team and will be based in Budapest. 

At the same time we are very sorry to be losing Caroline Lyall. Caroline has been with us for two years during which she has become a key member of our pre-clinical team. She is joining the QA team at Charles River Laboratories and we wish her all the best for the next phase of her career.