
PRO

Vadodara, India
Medical Device Regulatory Consultant | CDSCO Licensing & ISO 13485
Local Time - 02:09 AM
About Me
I am a Medical Device Regulatory Affairs professional with hands on experience in Indian medical device CDSCO compliance and Quality Management System ISO[removed]documentation. I support medical device startups, manufacturers, and innovators in navigating CDSCO regulatory requirements and implementing ISO[removed]compliant systems.
My key services include:
• CDSCO Test License MD 12 application support
• CDSCO Manufacturing License MD 3 / MD 7 application guidance
• Device Master File DMF and Plant Master File PMF preparation
• ISO[removed]Quality Management System QMS documentation and implementation support
All work is delivered with confidentiality, professionalism, and adherence to applicable regulatory standards. I look forward to helping you bring your medical device to market smoothly and compliantly.
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$9/hr
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