TGA Australian Medical Device Sponsorship / License Holding
gloizou
- Mar, 27, 2017
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As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If you […]
ISO 50001 Energy Management
- Nov, 10, 2016
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https://youtube.com/watch?v=1xfCvHLFAfE%3Ffs%3D1%26autoplay%3D1%26rel%3D0
Cosmetics GMP for Export Purposes (ISO 22716)
- Nov, 06, 2016
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If you are a cosmetics exporter, you may have had been notified by mandated bodies that you require to comply with EC Regulation 1223/2009. What are the requirements for this regulation? All cosmetic products exported to Europe/Asia/NZ will have to be produced according to Good Manufacturing Practices. Cosmetics Good Manufacturing Practices (GMP) is one of the […]
TGA Australian Medical Device Sponsorship
- Nov, 06, 2016
- Uncategorized
- Comments Off on TGA Australian Medical Device Sponsorship
As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If you […]
TGA Australian Medical Device Sponsorship – calling all overseas medical device manufacturers
- Nov, 06, 2016
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As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If you […]
TGA Australian Medical Device Sponsorship – calling all overseas medical device manufacturers
- Sep, 30, 2016
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As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If […]
TGA Australian Medical Device Sponsorship
- Sep, 30, 2016
- Uncategorized
- Comments Off on TGA Australian Medical Device Sponsorship
As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If you […]
Cosmetics GMP for Export Purposes (ISO 22716)
- Sep, 30, 2016
- Uncategorized
- Comments Off on Cosmetics GMP for Export Purposes (ISO 22716)
If you are a cosmetics exporter, you may have had been notified by mandated bodies that you require to comply with EC Regulation 1223/2009. What are the requirements for this regulation? All cosmetic products exported to Europe/Asia/NZ will have to be produced according to Good Manufacturing Practices. Cosmetics Good Manufacturing Practices (GMP) is one of the […]
TGA Australian Medical Device Sponsorship
- Sep, 30, 2016
- Uncategorized
- Comments Off on TGA Australian Medical Device Sponsorship
As per the Australian TGA Medical Device Regulations, before someone can supply a medical device for sale in Australia they are required to make an application to include the item in the Australian Register Therapeutic Goods (ARTG). The sponsor is the person or company responsible for the importation of therapeutic goods into Australia. If you […]
