TMQA Latest News

MHRA Updates Phase I Accreditation List

The MHRA updated their list of accredited phase I units in June 2015. The updated list can be found at:

The MHRA’s phase I accreditation scheme is a voluntary scheme for organisations conducting phase I clinical trials, in particular for those conducting first in human (FIH) trials. Organisations in the scheme have to exceed the basic regulatory good clinical practice (GCP) standards for avoiding harm to trial subjects and for handling any medical emergencies.

Addendum to ICH E6

Since the adoption of the ICH E6 Guideline on Good Clinical Practice (GCP) in 1996, clinical trials have evolved substantially, with increases in globalisation, study complexity and technological capabilities. To keep pace with the scale and complexity of clinical trials and to ensure appropriate use of technology, the approach to GCP should be modernised to enable implementation of innovative approaches to clinical trial design, management, oversight, conduct, documentation, and reporting that will better ensure human subject protection and data quality. Although ICH E6 generally has been interpreted as providing sponsors flexibility to implement innovative approaches, it has been misinterpreted and implemented in ways that impede innovation by, for example, emphasising less important aspects of trials (e.g. focusing on the completeness and accuracy of every piece of data) at the expense of critical aspects (e.g. carefully managing risks to the integrity of outcome data). Modernising ICH E6 by supplementing it with additional recommendations will better facilitate broad and consistent international implementation of new methodologies. As a result, an addendum to ICH Topic E6 (Good Clinical Practice) was endorsed by the ICH Steering Committee in June 2014 and the last face-to-face ICH E6 Expert Working Group (EWG) meeting took place in Japan in June 2015 during which the work plan was updated as follows




Jun 2015

Face to face meeting

·         Agreed on the addendum language and reached Step 1 draft

·         Updated the work plan

Jul 2015-Jan 2016

Public consultation by ICH and regional regulators

·         Gathering comments for review

Sep–Nov 2015

Webconferences (3)

·         Reviewing and resolving comments received form public consultation

Dec 2015

Face to face meeting

·         Resolve public comments and start drafting final document

EMA Update on Publication of Clinical Trial Data

On 24 June 2015, the EMA held a webinar to provide an update on the implementation of its policy on the publication of clinical data which came into effect on 01 January 2015. The topics covered in the webinar included an explanation of the principles for the submission of redacted clinical reports, the redaction consultation progress as well as guidance on what is and is not considered commercially confidential information and on the anonymisation and redaction of personal data in clinical reports. The video recording of the webinar as well as slides of all the presentations given have now been published on the EMA website and can be found on:

TMQA strengthens partnership with BioCity Scotland

We are delighted to announce that TMQA has strengthened its relationship with BioCity Scotland by upgrading from Service Associates to Corporate Partners.  As Service Associates the TMQA team provided an onsite “drop in” QA advice service for tenants two days a month.   Over the last two years, we have supported several tenants by providing advice on regulatory requirements and compliance, supporting the implementation of quality management systems and conducting independent GMP (Good Manufacturing Practice) audits.

TMQA Director, Andrew Waddell, commented: “Developing a closer relationship with Biocity and its tenants gives them access to a range of Quality Assurance services which can change and develop along with their companies.  Using our ‘pay-as-you-go’ service means that they don’t need to invest in the overhead costs of hiring their own QA staff – they can use TMQA services whenever they need and only pay for the actual time involved.   Active partnering with organisations – small or large – is at the core of our business plan and our relationship with Biocity is an exciting development for us.”

Clinical Quality Assurance – Career Development Opportunities

TMQA is looking to expand its team of Clinical Quality Assurance (CQA) professionals.

Your Background

Applicants should have a minimum of 3 years’ relevant experience.  This experience will ideally be in CQA, however, we are also keen to offer career development opportunities to applicants in other areas of clinical research (eg. CRAs) who would like to move into CQA.

The Job

The major part of the job will be undertaking audits of clinical trials, usually at investigator sites.  The job will involve travel in the UK and Europe with the possibility of travel further afield.  Typically you will conduct two audits per month each of which will involve 2-3 days on site.

Relevant experience in clinical trials is essential as well as an ability to work independently (after initial training).  You will have the personal skills to interact professionally with clinical research staff at all levels.  A key element will be to analyse the evidence gathered during the audit and present findings clearly and concisely both verbally and in a written report.


We have offices in Edinburgh and Bratislava.  Staff who are transitioning into QA would need to be based in one of these offices.  Home-based positions will be considered for staff who are already experienced CQA Auditors.


For further information please contact