The medical device and diagnostic industry operates in a highly regulated environment to ensure the consistency of the product manufactured. Within IMDA, two groups act in tandem to lobby on behalf of the sector on regulatory and quality issues. IMDA’s Regulatory Steering Committee informs regulatory policy on behalf of members and lobbies at the most senior level both nationally and in Europe, interacting with the EU Commission, Council and members of the European Parliament. IMDA’s QA/RA Forum, along with IMDA’s Regulatory Steering Committee, lobbies on behalf of the sector acting as a conduit for information on regulatory issues. The Forum provides regular opportunities for learning and networking for QA/RA professionals in the sector.