Timian is dedicated to quality and regulatory compliance consulting to medical device companies. Tailor-made approach allows us providing with individual and personalized solutions, when assuring assistance with technical file or design dossier, training, auditing and assuring compliance with MDD 93/42/EEC, new MDR, 21 CFR 820, ISO 13485, sterilization, microbiology, risk management…
Company’s Keywords:
medical devices, consulting, life science, project management, technical experts
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