According to the survey (PDF), 78% of medical device company respondents do not have a sufficient understanding of the EU MDR, while 58% said they had no strategy in place to fix gaps in their clinical data or collection processes. Additionally, 39% of organizations have not yet identified a Person Responsible for Regulatory Compliance, a new role required by the MDR.

The EU updated its regulations in 2017 covering product evaluation, with more stringent procedures aimed at ensuring the rejection of unsafe or noncompliant equipment.

KPMG and RAPS suggest that device manufacturers evaluate the sturdiness of their products’ clinical evidence and address changes that need to be made in the recertification process for existing products. They also recommended that companies build cross-functional teams from quality assurance, supply-chain management and regulatory compliance to tackle the issues.

“Preparing for the EU MDR is a major challenge for medical device companies in the European market,” said RAPS Executive Director Paul Brooks. “And while there is still a great deal of uncertainty surrounding regulators’ interpretations and expectations, those who are proactive in developing regulatory strategies and contingency plans will very likely find themselves in the strongest position when the 2020 deadline arrives.”

KPMG and RAPS’ survey gathered 220 responses in June from regulatory affairs or quality-assurance professionals, with 36% from companies with less than $10 million in annual revenue. Another 36% of respondents came from organizations with annual revenues between $10 million and $999 million, while the remaining 28% were from those with more than $1 billion.

Source: FierceBiotech