Medical Device CE Certification and ISO 13485 QMS Process Consultancy

Business DevelopmentCarrying out new product development activitiesCarrying out strategic activities to expand into new marketsNegotiations with various companies on product-based partnershipsContinuous communication with investors, TTGV, Ministry units, customers, sector related associations, etc.Project Management (Ministry of Industry Teknogirişim ve TÜBİTAK 1507)Technical and financial feasibility, budget management, team management, time managementR&D -… Show more Business DevelopmentCarrying out new product development activitiesCarrying out strategic activities to expand into new marketsNegotiations with various companies on product-based partnershipsContinuous communication with investors, TTGV, Ministry units, customers, sector related associations, etc.Project Management (Ministry of Industry Teknogirişim ve TÜBİTAK 1507)Technical and financial feasibility, budget management, team management, time managementR&D - Structural Analysis ExpertiseAnalysis of critical product part strengths with Ansys programCreating and Managing the Company BudgetIncentive Certificate ExpertiseMinistry of Industry, TÜBİTAK 1507, TÜBİTAK 1501, Türkiye Teknoloji Geliştirme Vakfı(TTGV) Hit Program and KOSGEB support program files and follow-up of the processISO13485:2016 Responsibility for obtaining the Quality Management System Certificate and the implementation processMedical device product CE certification process responsibility Show less

Business DevelopmentContinuous communication with investors, Ministry units, sector-related associations, etc.Project Management (TÜBİTAK 1512)Technical and financial feasibility, budget management, team management, time managementMultidisciplinary team managementManaging Financial and Administrative AffairsManaging the sale process of the company to investorsCompany External Relations Responsibility