Subject: Medical Device Regulation 2017/745 (MDR), Clinical Evaluation, Post-Market Surveillance (PMS), Clinical Investigation (CI), Post-Market Clinical Follow-up (PMCF)

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Year: 2019

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Type: Article

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Title: Providing clinical evidence under the MDR 2017/745 – new challenges for manufacturers in medical device industry

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Author: Ivanovska E., Tonic Ribarska J., Lazova J., Popstefanova N., Davcheva Jovanoska M., Trajkovic Jolevska S.

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Abstract: Short communication

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Publisher:

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Relation: Arhiv za farmaciju

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Identifier: oai:repository.ukim.mk:20.500.12188/23690
Identifier: 2217-8767
Identifier: http://hdl.handle.net/20.500.12188/23690

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