

"Quality and regulatory compliance support for medical device and life science companies"
Collocco Consultancy provides quality, compliance, and regulatory affairs expertise to medical device and life science companies navigating complex regulatory frameworks. Founded in Wales in 2018, the firm delivers hands on support for Quality Management Systems, technical file preparation, audit readiness, and global regulatory strategy. The company operates through a core team of IRCA certified auditors backed by specialist consultants. The consultancy works with organisations at every stage, from startups preparing for first certification to established companies remediating compliance gaps. Services include ISO13485 QMS implementation, CE and UKCA marking support, and regulatory submissions across EU, UK, US, and international markets.


5
Team Members
2018
Founded
Consulting
Sector
Hybrid
Work Environment
A medical device industry where regulatory compliance enables innovation rather than constraining it, and where companies of all sizes can confidently bring safe, effective devices to patients worldwide.
Collocco Consultancy helps medical device and life science companies achieve regulatory compliance and certification through expert quality management, technical file preparation, and regulatory affairs support.