Product Inspection and Supervision

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Product Registration
All manufacturers or importers of health products and PPE must register their products with BPOM to obtain a distribution permit before they can be sold on the market. This registration process ensures that the product has gone through testing and evaluation to ensure its safety and complies with specified requirements.

Product Test and Evaluation
Before health products and PPE can be given distribution permits, BPOM carries out product tests and evaluations to ensure that the products are safe to use and do not have adverse side effects. Tests and evaluations are carried out based on requirements set by BPOM and can involve several stages of testing, such as laboratory testing MobileNumberList clinical testing.



After health products and PPE are given distribution permits and sold on the market, BPOM continues to carry out inspections and supervision to ensure that the products still meet the specified safety and quality standards. This inspection and supervision is carried out regularly and includes taking product samples from the market for further testing.

Reporting System
BPOM has a reporting system to receive reports from the public regarding problems that occur with health products and PPE sold on the market. The public can report this problem via the official BPOM website or via the BPOM call center. The report will then be followed up by BPOM in accordance with established procedures.

Conclusion
The Medical Device Monitoring System and PKRT are regulatory systems that are very important in maintaining public health and safety in Indonesia. With this system, people can have more confidence and trust in the health products and PPE they use, as well as prevent products that are unsafe for consumption or use. Therefore, we all need to pay attention to and comply with existing regulations and use health products and PPE wisely.Crew Management System: Solution for Effective Ship Crew Management.