Laws and Regulations

Act on Medicinal Products

Medicinal Products Act, No. 100/2020 Act on Medicinal Products

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Act on Medical Devices

Act on Medical Devices No. 132 2020 Act on Medical Devices

Open

Act on Product Safety and Official Market Control No. 134/1995 Act on Medical Devices

Open

Acts on Healthcare

Act on Health Security and Communicable Diseases, No. 19/1997 Acts on Healthcare

Open

Act on Health Insurance, No. 112/2008 Acts on Healthcare

Open

Act on Scientific Research in the Health Sector, No. 44/2014 Acts on Healthcare

Open

Health Service Act, No. 40/2007 Acts on Healthcare

Open

Act on Narcotics

Narcotics Act, No. 65/ Act on Narcotics

Open

Acts on Social Security

Act on Patient Insurance No. 111/2000 Acts on Social Security

Open

Social Security Act, No. 100/2007 Vefeyðublað Acts on Social Security

Open

Acts on Administrative Predures and Information

Administrative Procedures Act, No. 37/1993 Acts on Administrative Procedures and Information

Open

The Information Act, No. 140/2012 Acts on Administrative Procedures and Information

Open

Regulations on Medicinal Products

Regulation concerning Marketing Authorisations for Natural Medicinal Products and Registration of Traditional Herbal Medicinal Products, No. 142/2011 Regulations on Medicinal Products

Open

Regulation concerning the Manufacture of Medicinal Products, No. 893/2004 Regulations on Medicinal Products

Open

Regulation on the Importation by Individuals of Medicinal Products for their own Use, No. 1277/2022 Regulations on Medicinal Products

Open

Regulation on Marketing Authorisations for Propietary Medicinal Products, their Labelling and Package Leaflets, No. 545/2018 (in icelandic only) Regulations on Medicinal Products

Open

Regulations on Clinical Trials

Regulation on Clinical Trials of Medicinal Products in Humans Regulations on Clinical Trials

Open

Regulation on Narcotics

Regulation on Habit-forming and Narcotic Substances and Other Controlled Substances, No. 233/2001 Regulation on Narcotics

Open

Regulations on Medical Devices

Regulation on instructions for use for medical devices, No. 630/2022 (in icelandic only) Regulations on Medical Devices

Open

Regulation on reprocessing of single use devices, No. 1154/2021 (in icelandic only) Regulations on Medical Devices

Open

Regulation on In Vitro Medical Devices, No. 936 (in icelandic only) Regulations on Medical Devices

Open

EU regulation on in vitro diagnostic medical devices, No. 2017/746 (in icelandic only) Regulations on Medical Devices

Open

EU regulation on medical devices, No 2017/745 (in icelandic only) Regulations on Medical Devices

Open

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Act on Medicinal Products

Medicinal Products Act, No. 100/2020 Act on Medicinal Products

Act on Medical Devices

Act on Medical Devices No. 132 2020 Act on Medical Devices

Act on Product Safety and Official Market Control No. 134/1995 Act on Medical Devices

Acts on Healthcare

Act on Health Security and Communicable Diseases, No. 19/1997 Acts on Healthcare

Act on Health Insurance, No. 112/2008 Acts on Healthcare

Act on Scientific Research in the Health Sector, No. 44/2014 Acts on Healthcare

Health Service Act, No. 40/2007 Acts on Healthcare

Act on Narcotics

Narcotics Act, No. 65/ Act on Narcotics

Acts on Social Security

Act on Patient Insurance No. 111/2000 Acts on Social Security

Social Security Act, No. 100/2007 Vefeyðublað Acts on Social Security

Acts on Administrative Predures and Information

Administrative Procedures Act, No. 37/1993 Acts on Administrative Procedures and Information

The Information Act, No. 140/2012 Acts on Administrative Procedures and Information

Regulations on Medicinal Products

Regulation concerning Marketing Authorisations for Natural Medicinal Products and Registration of Traditional Herbal Medicinal Products, No. 142/2011 Regulations on Medicinal Products

Regulation concerning the Manufacture of Medicinal Products, No. 893/2004 Regulations on Medicinal Products

Regulation on the Importation by Individuals of Medicinal Products for their own Use, No. 1277/2022 Regulations on Medicinal Products

Regulation on Marketing Authorisations for Propietary Medicinal Products, their Labelling and Package Leaflets, No. 545/2018 (in icelandic only) Regulations on Medicinal Products

Regulations on Clinical Trials

Regulation on Clinical Trials of Medicinal Products in Humans Regulations on Clinical Trials

Regulation on Narcotics

Regulation on Habit-forming and Narcotic Substances and Other Controlled Substances, No. 233/2001 Regulation on Narcotics

Regulations on Medical Devices

Regulation on instructions for use for medical devices, No. 630/2022 (in icelandic only) Regulations on Medical Devices

Regulation on reprocessing of single use devices, No. 1154/2021 (in icelandic only) Regulations on Medical Devices

Regulation on In Vitro Medical Devices, No. 936 (in icelandic only) Regulations on Medical Devices

EU regulation on in vitro diagnostic medical devices, No. 2017/746 (in icelandic only) Regulations on Medical Devices

EU regulation on medical devices, No 2017/745 (in icelandic only) Regulations on Medical Devices

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