clinOXY provides expert support in regulatory writing specialized in Medical Device Regulatory Documentation such as Design History Files, Technical Documentation, Instruction for use, Surgical Technique Guide, SMPC (Summary of Medicinal Product Characteristics), SOTA, Clinical Evaluation Reports, EUDAMED implementation and SSCP (Summary of Safety and Clinical Performance. Our specialized team offers comprehensive assistance in preparing regulatory documents, including submissions, reports, summaries, and dossiers, adhering to stringent regulatory guidelines and standards.