You can rely on IMIC for collection of medical device safety information!
DEVICE SAFETY BASE (DSB) is an information collection service specialized in medical device safety, offered exclusively by IMIC, which has established a system for contract safety assurance and quality management in accordance with GVP standards.
Leveraging our many years of operational experience, we serve as the foundation (BASE) for collecting medical device safety information (DEVICE SAFETY) and support the safety management operations of medical device manufacturers.
Overview of Medical Device Safety Information Surveillance (DEVICE SAFETY BASE)
Leveraging IMIC’s distinctive search technology and quality control expertise, we provide comprehensive support for the collection of medical device safety information.
Our qualified search specialists, who have extensive experience
in the medical device industry, will assist you in developing search queries to meet your specific needs and will also perform regular maintenance on these queries.
We have established a robust quality management system that covers the search queries themselves and the history of query changes, enabling us to quickly provide the necessary documentation for compliance inspection and audits (documentation is provided for a fee).
You can receive relevant information on a regular basis without needing direct corporate subscriptions to major domestic and global databases with proven track records in medical device safety.
One of Japan’s leading medical databases, created by the NPO Japan Medical Abstracts Society.
The most prominent international database for collecting medical literature data, created by the U.S. National Library of Medicine (NLM).
A database containing the latest information in the biomedical field, created by the European academic publisher "Elsevier".
*Available only when you apply for MEDLINE.
We monitor the websites of regulatory authorities in six major countries on a daily basis and provide weekly updates in an easy-to-understand summary format—complete with Japanese digests—covering medical device recalls, safety warnings, and other relevant information.
Since we cover a wide range of medical device topics, there is no need to register keywords to use this service.
This service is ideal for collecting overseas measures information, as well as for your daily research, including information on products from other companies.
U.S. FDA Center for Devices and Radiological Health
UK Medicines and Healthcare Products Regulatory Agency
French National Agency for Medicines and Health Products Safety
German Federal Institute for Drugs and Medical Devices
Australian Therapeutic Goods Administration
Health Canada
※Some pages are not included.
Implementation Flow for Medical Device Safety Information Surveillance (DEVICE SAFETY BASE)