Business Data

Medical Device Regulations - Indonesia - Q4 2017

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The registration of medical devices is carried out by the Directorate General of Pharmaceutical Services and Medical Devices (Dirjen Binfar dan Alkes), within the MoH. The registration of medical devices is currently implemented through Regulation No. 1190/MENKES/PER/VIII/2010 Regarding Marketing Licence of Medical Devices and Household Products.

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Ketersediaan

Informasi Detail

Judul Seri

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No. Panggil

BD BMI m

Penerbit

London : BMI Research., 2017

Deskripsi Fisik

3 p.

Bahasa

English

ISBN/ISSN

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Klasifikasi

BD

Tipe Isi

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Tipe Media

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Tipe Pembawa

online resource

Edisi

Q4 2017

Subjek

Medical
Device
Regulations

Info Detail Spesifik

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Pernyataan Tanggungjawab

BMI Research

Versi lain/terkait

Lampiran Berkas

Komentar

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