Category: Regulation

New research reveals participants’ experiences of the GDC’s Fitness to Practise process

The General Dental Council (GDC) today published two research reports that deepen understanding of fitness to practise (FtP), providing valuable insight into how the process could be further improved for participants. As part of its commitment to improving the FtP process, the GDC commissioned two research projects, led by the University of Manchester, to understand
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GDC publishes ambitious new strategy to build trust and transform dental regulation

The General Dental Council (GDC) today published its new strategy 2026-2028, committing to significant change and improvement over the next three years – and towards 2030.  The GDC’s vision is to be a trusted and effective regulator, supporting dental professionals to provide safe and effective care for their patients. To do this, the GDC will champion a model
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GDC announces new alternative evidence policy to support refugee and displaced dental professionals

The General Dental Council (GDC) has today announced a new policy to accept alternative forms of evidence from refugee and displaced dental professionals, removing unnecessary barriers for those unable to provide standard documentation due to circumstances beyond their control. The policy will apply to dentists with international qualifications pursuing exam-based routes to join the GDC
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Reminder – GDC Annual Retention Fee

A gentle reminder that the GDC Annual Renewal takes place in the weeks leading up to 31st July.   The three actions to complete your Annual Renewal process are:   Make an Indemnity Declaration Pay the Annual Retention Fee (ARF) Make a Continuing Professional Development (CPD) statement   DLA members have received further information via
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MHRA Devices – Registration Renewal Reminder

It has been brought to our attention that the MHRA have started to contact registrants via email regarding ‘Registration Renewal Reminder’ It is a legal requirement to inform the MHRA of any changes to your registration per section 7A (general medical devices), section 33A (in vitro diagnostic medical devices) and section 21A (active implantable medical
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