15 Sep
|
Maven Profcon Services
|
Ahmedabad
15 Sep
Maven Profcon Services
Ahmedabad
- 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)
🏢 Maven Profcon Services
📍 Ahmedabad