Health Products
Health Products
| 311 | Re: Rules, procedures and conditions on display of labels and medical device package inserts, B.E. 2563 (2020) |
| 312 | Re: Rules, procedures and conditions for preparation of reports on medical device malfunctions or adverse events occurring to consumers and reports on field safety corrective actions for medical devices, B.E. 2563 (2020) |
| 313 | Re: Risk classification of medical devices, B.E. 2562 (2019) |
| 314 | Re: Classes of medical devices or medical devices of which manufacturers or importers are required to declare specifications (no. 2), B.E. 2563 (2020) |
| 315 | Re: Prescribing rules, procedures and conditions on registration of medical device manufacturing establishments, B.E. 2552 (2009) |
| 316 | Re: Specification of standards and evaluation of test kits and reagents related to diagnosis of sars-cov-2 (virus causing covid-19) infection, B.E. 2564 (2021) |
| 317 | Cosmetics Act (No.2), B.E. 2565 (2022) |
| 318 | Re: rules, procedures and conditions on requirements for persons manufacturing for sale, persons importing for sale or contract manufacturers to collect information pertaining to cosmetics for inspection, B.E. 2560 (2017) |
| 319 | Re: Rules, procedures and conditions on the manufacture or importation of cosmetics, B.E. 2561 (2018) |
| 320 | Re: Notification, issuance of notification receipts, renewal of notification receipts, variation of particulars of notification receipts and issuance of replacements of notification receipts of cosmetics, B.E. 2561 (2018) |
