Hsa product registration search
WebA A A Registered Health Products Find out if your Medicines/Medical Devices/Chinese Proprietary Medicines are registered/listed in Singapore PRODUCT NAME * Forensic …
Hsa product registration search
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Web22 jul. 2024 · The Health Sciences Authority (HSA), Singapore’s regulatory agency in the sphere of healthcare products, has published a guidance document dedicated to Class A medical devices exempted from product registration. Web31 dec. 2024 · Find out how to register your therapeutic product and manage the product registration here. Registration overview Understand the therapeutic product …
WebIn 2007, the HSA passed the Health Products Act, allowing them to conduct mandatory product registration and regulate the supply, distribution, manufacturing, import, and advertisement of all health products. Registered medical devices are listed on the Singapore Medical Device Register (SMDR), which is publicly available on the HSA’s … Web16 mrt. 2024 · The Health Sciences Authority (HSA), Singapore’s regulatory agency in the sphere of healthcare products, has published a guidance document dedicated to the grouping of medical devices for product registration.
WebHsa product code Text (General) "-" : Data is negligible or not significant WebIn Singapore, therapeutic products, known as western medicines, are required to be registered with the Health Sciences Authority (HSA) before they can be supplied in Singapore. The Health Products Act (HPA) regulates the manufacture, import, supply, presentation and advertisement of therapeutic products. Therapeutic Product Definition:
WebAlthough Class A nonsterile medical devices are legally exempted from - product HSA’s registration requirement, importers are required to be licensed by HSA and the Medical Device Importer’s licence number should be indicated in the CA/SC Code 1 field. 13.
WebProduct Regulations. Medical devices; Therapeutic products; Health supplements; Traditional medicines; Chinese proprietary medicines; Cosmetic products; Tobacco … cf-rz4 バッテリー 赤点滅WebThe Health Sciences Authority (HSA) Singapore has published the updated guidance document on the regulatory processes and requirements for therapeutic product registration in August 2024. HSA has updated the details on pre-submission consultation, whereby the range of mechanisms available to companies is explained in detail. cfrz4 パナソニックWeb8 aug. 2024 · HSA has announced the implementation of the Class A Medical Device Register for public access on 10 August 2024.This register allows members of the public to search for importers/local manufacturers as well as imported/manufactured Class A medical devices that are exempted from product registration. All devices on the Class A … cf-rz4 メモリ8gbWebStep 2. Identify the conformity assessment procedure that must be taken. This could be self-declaration, involve testing, inspection or quality system assessment from a Notified Body or a combination of these. The conformity assessment procedure will differ depending on your product and the Directive in respect of which you will be CE Marking. cf-rz4 メモリー交換Web1 - Search for Products Specifying Authorisation Features: This search provides details of current Authorisations. Selecting this link will display the Product search page shown … cf-rz5 ドライバーWebThe proximity of Singapore to other Asian countries also adds to its attraction as a platform for launching new products. In Singapore, cosmetic product registration is obtained … cf rz4 メモリ増設WebThe proximity of Singapore to other Asian countries also adds to its attraction as a platform for launching new products. In Singapore, cosmetic product registration is obtained from the Singapore Health Authority - Health Sciences Authority (HSA). As a proven Regulatory partner, Freyr is specialized in cosmetics registration in Singapore ... cfrz5 ドライバ