
Sundal Ali
Sundal Ali
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Manager Regulatory Affairs
Shukla Medical • Full time
Aug 2024 - Present • 2 yrs 1 mo
Managed medical device regulatory affairs and compliance activities. Supported DRAP medical device registration, product licensing, and establishment licensing. Worked on regulatory compliance according to Medical Device Rules, 2017. Prepared and reviewed technical files, design dossiers, and regulatory documentation. Supported FDA medical device regulatory requirements and 510(k) submissions. Worked with EU MDR 2017/745 and ISO 13485:2016 requirements. Liaised with regulatory authorities and supported organizational regulatory obligations. Contributed to QMS and regulatory compliance documentation. Key Achievements: Built professional expertise in medical device regulatory affairs and compliance. Developed experience in DRAP registration, licensing, and regulatory submissions. Gained expertise in ISO 13485 QMS and medical device regulatory documentation. Developed experience supporting EU MDR and FDA requirements, including FDA 510(k). Prepared and managed technical files and design dossiers. Developed strong capabilities in regulatory documentation, compliance, and technical review. Demonstrated leadership, problem-solving, collaboration, adaptability, and team-management skills.