Develop and implement regulatory strategies to ensure compliance with EU MDR 2017/745.
Prepare and review regulatory submissions, including technical documentation and clinical trial applications.
Collaborate with cross-functional teams to ensure timely and successful product approvals.
Conduct thorough reviews of regulatory documents to identify areas for improvement.
Provide guidance and support to internal stakeholders on regulatory matters related to EU MDR 2017/745.
Stay up-to-date with changes in regulatory requirements and industry trends.
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📌 Sr Regulatory Executive Ahmedabad (India)
🏢 Maven Profcon Services
📍 India
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