Pacific Bridge Medical - China Medical Publications
New Japanese Medical Device Regulations After April 1, 2005 Through January 20, 2006: A more comprehensive explanation than our January 26, 2006 webcast on Japan
Published by Pacific Bridge Medical	Print Article

	Price: $750

This report provides a detailed overview of Japan’s most recent medical device regulations from April 2005 to January 2006. This report is 47 pages. Click here to view a sample page.

Table of Contents :

• Master File Registration
• Applying for a Foreign Manufacturer Certificate
• New Labeling Requirements
• Licensing System for Medical Device Companies
• New Regulations for Conducting Medical Device Clinical Trials (GCP)
• GCP Compliance Review
• Adverse Events Reporting Requirements
• Information System for Safety Countermeasures
• CHUIKYO: Central Social Insurance Medical Council
• New Requirements for Medical Device Reimbursement
• Post-Marketing Safety Measures (GVP)
• Good Post-Marketing Study Practice (GPSP)
• Standards for Quality Assurance (GQP)
• New GLP Updates
• PMDA Consultations
• Timeline for PMDA Review

Order now and we will ship you this report at NO ADDITIONAL CHARGE.

• Price: $750.00.

Click here to purchase this report.

Contact us at researchstore@pacificbridgemedical.com if you have any questions.

Read more >> Publications Index

Go to Home