What is the meaning of the mask drug monitoring record?
This mask is a medical mask, there is anti-virus efficacy
Drug Administration can not find the record is fake?
Not necessarily.
In the State Food and Drug Administration database, there are records that include all domestic or imported drugs and health products. So if you can't find an "approval number" on this site, you're looking at a fake drug or a fake health product.
But the food is the provincial approval, so in the State Food and Drug Administration database is not found.
Drug sales record management regulations?
Every drug business enterprise should be to the local drug supervision department for drug purchasing, sales staff for the record.
Business enterprise drug sales personnel filing system refers to: (Jiangsu Taizhou as an example)
Verify the drug business enterprise sales personnel legal person entrusted power of attorney, labor contract, ID card and other materials, the establishment of enterprise sales personnel basic database.
The salespersons who are engaged in illegal activities without registration, beyond the scope of authorization, and falsification of business qualifications will be recorded in the "blacklist of drug salespersons" and punished in accordance with the law once they are found; and those who constitute crimes will be handed over to the judicial organs to be investigated in accordance with the law. At the same time, the illegal sale of drugs related to the enterprise and its legal representative, the quality of the person in charge together with the "drug business enterprise blacklist", and to the public.
It is required that all drug companies to conduct a comprehensive inventory of sales staff, and shall not provide business licenses, drug licenses and GSP certificates and other relevant qualification materials for sales staff who have not signed employment contracts with the company.
What is the process of a Class III medical device recall?
Third-level recall: the use of the medical device causes less likelihood of harm, but still need to be recalled (7 days).
Process:
1, after the decision to recall, should be able to file a record with the Drug Administration in 5 days:
Imported: overseas manufacturers should notify its designated agent in China to report to the State Drug Administration in a timely manner.
Domestic: the manufacturer promptly report the location of the provincial drug supervision.
Changes in the recall program, the timely filing of the original report to the Pharmacovigilance.
2, the recall process, should regularly want to drug supervision department to submit a report on the implementation of the recall plan.3, the enterprise's handling of the recalled medical devices should have a detailed record, and submit a report to the medical device manufacturer where the provincial drug supervision department.4, need to be destroyed, it should be destroyed in the destruction of the location of the drug supervision department under the supervision of the destruction.5, after the completion of the recall, 10 days was to the original drug supervision department Submit a summary report of the recall. 6, the drug regulatory department shall receive the summary report within 10 days from the date of review of the report, and evaluation of the effectiveness of the recall:
Evaluation passed;
Evaluation did not pass, if the review and evaluation, the artificial recall is not complete, has not yet been effective in eliminating the defects, then the enterprise needs to be re-recalled.
7. Failure to comply with the provisions of the recalled products will be subject to a series of penalties, such as warnings, ordered to make corrections within a certain period of time, fines and other punitive measures.
What does Taobao with a FDA filing mean?
It means that the business of buying drugs on Taobao has been filed with the FDA so that you can buy with confidence.