※This release provides information regarding our policy for organizing publicly available information concerning the manufacturing background of Glamour Snoer.
※This is not a strong recommendation for any specific product, procedure, treatment, decision to introduce, or use.
※The content published is based on objective public information collected by our company and does not directly guarantee the legal status of individual devices in Japan (approval, certification, notification, etc.), nor specific efficacy, effectiveness, or safety.
MEDLAC Instrument and Consulting Co., Ltd. (Head office: Fukuoka City, Fukuoka Prefecture; Representative Director: Hideki Ogawa) is disseminating information in the medical slimming field and related devices by organizing basic public information.
We are pleased to announce that important public information directly related to the manufacturing background and quality management system of "Glamour Snoer," one of the subjects of our information organization, has been confirmed. This is being shared along with our company's basic stance.
Regarding the Acquisition of "MDSAP" Certification by Glamour Snoer's Manufacturer
Through our public information research, it has been confirmed that the manufacturer of "Glamour Snoer," a name frequently seen in various public documents in the medical slimming field, has acquired "MDSAP (Medical Device Single Audit Program)" certification.
MDSAP is a program where a single auditing organization, recognized by regulatory authorities of participating countries, audits the quality management systems of medical device manufacturers based on international standards.
At our company, when organizing various device-related information in circulation, we position such "objective audit status of the manufacturer's quality management" as one of the highly beneficial facts for medical professionals to accurately understand the background of devices.
Importance of Objective Facts in Information Verification
The internet contains a mixture of information regarding many related functions and devices, and many are limited to names and fragmented descriptions of effects.
Therefore, when verifying information, it is crucial to confirm not only claims about individual effects and efficacies but also comprehensive background information such as:
・What kind of quality management system the manufacturer has established
・Whether it has undergone an objective audit program by a third party like MDSAP
・Whether the information's source and update time are clear
This is key to making appropriate judgments without misunderstanding the legal positioning. Our company will continue to recommend careful information organization centered on such "objective facts regarding manufacturing background," rather than exaggerating specific efficacies.
MEDLAC Instrument and Consulting Co., Ltd.'s Approach
As a company engaged in the medical device sales business, MEDLAC Instrument and Consulting Co., Ltd. emphasizes transparency in information related to the medical field.
Our basic stance for disseminating information on medical devices is:
・To avoid excessive expressions
・To organize information based on facts
・To create an information environment where medical professionals can make appropriate judgments
・To handle information in a way that clarifies its source and preconditions
We will continue to work on the appropriate organization and provision of device information in the medical field.
【About MEDLAC Instrument and Consulting Co., Ltd.】
MEDLAC is an "overseas medical device information provider" that supports clinic management in areas such as medical device introduction and information organization with a specialized team.
Company Name
MEDLAC Instrument and Consulting Co., Ltd.
Representative
Representative Director Hideki Ogawa
Location
4-45-25 Kashiiekihigashi, Higashi-ku, Fukuoka City, Fukuoka Prefecture
Establishment Date
February 2020
Business Activities
Knowledge Provision, Medical Device Sales Business
URL
https://www.medlac.net/
FACT BOX
- Source: PR TIMES
- Category: News