Scrip is part of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

Japan's MHLW Panel Awards Orphan Status To Century Medical Artificial Heart, Panasonic PDT Semiconductor Laser

This article was originally published in PharmAsia News

Executive Summary

TOKYO - Japan's Pharmaceutical and Food Sanitation Council's subcommittee on medical devices and in vitro diagnostics has approved two devices for orphan diseases and three others, Takeshi Baba, manager of the General Affairs Division of the Ministry of Health, Labor and Welfare's Pharmaceutical and Food Bureau told PharmAsia News Dec. 12

You may also be interested in...



Japan's MHLW Will Triple Review Officers To Shorten Device Lag

TOKYO - Responding to foreign criticisms about a long medical device approval lag, Japan's Ministry of Health, Labor and Welfare will implement several measures, including tripling the number of examination officers beginning in fiscal 2009 (which begins next April), as part of a new medical examination acceleration action program, a ministry official said Dec. 16

Japan's MHLW Will Triple Review Officers To Shorten Device Lag

TOKYO - Responding to foreign criticisms about a long medical device approval lag, Japan's Ministry of Health, Labor and Welfare will implement several measures, including tripling the number of examination officers beginning in fiscal 2009 (which begins next April), as part of a new medical examination acceleration action program, a ministry official said Dec. 16

MHLW Drafts GCP Guidance To Strengthen Human Subject Protections For Device Trials

TOKYO - Japan's Ministry of Health, Labor and Welfare Nov. 11 posted a draft ministry ordinance on good clinical practices that would strengthen the country's human subject protections for participants in clinical device trials. The measure calls for independent institutional review boards to approve device trials

Related Content

UsernamePublicRestriction

Register

SC067427

Ask The Analyst

Please Note: Click here for more information on the Ask the Analyst service.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel