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Mark J.
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+14
Operon Strategist is working towards catalyzing and ensuring the strategic development of the clients in the areas of Regulatory approvals , Quality Assurance, Quality Control, Licensing for the Medical Devices industry. We undertake turn key projects, annual regulatory contract as well as functions on the customized packages as per the need of the client. Medical Device Project consultancy services with 20+ years of experience in Handling regulatory projects Strong knowledge of Medical Device Regulatory and Primary packaging Regulations , Expertise in the Medical Device Layout design ,Clean Room Design and Process Validation , Medical Device Design And Development , Medical...
Medical device turnkey project consultant,plant layout design consultant,clean room design consultant,us fda consultant,ce mark consultant,iso 13485 consultant,iso 15378 consultant,primary packaging project consultant,us fda 21 cfr part 211,us fda 21 cfr part 210,us fda registration,cdsco import license,fda consultant,us fda 510 k clearance,fda 510(k),tga registration,anvisa registration,design and development of medical devices,and combination device manufacturing
Operon strategist | medical device consultancy, cdsco, 510 k consultancy, turnkey project consultant operates in the Business consulting and services industry.
Operon strategist | medical device consultancy, cdsco, 510 k consultancy, turnkey project consultant's revenue is 11m - 100m
Operon strategist | medical device consultancy, cdsco, 510 k consultancy, turnkey project consultant has 11 - 50 employees.
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