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(newest | oldest) View (newer 50 | older 50) (20 | 50 | 100 | 250 | 500)- 12:09, 9 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx (Authorization for medical devices mandatory problem, foreign risk notification, and recall reporting according to sections 61.1, 61.3 and 65.1 of the Medical Devices Regulations and/or designation to Act as the Canadian regulatory contact)
- 12:09, 9 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx (Authorization for medical devices mandatory problem, foreign risk notification, and recall reporting according to sections 61.1, 61.3 and 65.1 of the Medical Devices Regulations and/or designation to Act as the Canadian regulatory contact)
- 15:46, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Questions and Answers FRN FINAL FR.pdf
- 15:46, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Questions and Answers FRN FINAL FR.pdf
- 15:45, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Deck Info Session Feb 2021 FINAL FR.pdf
- 15:45, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Deck Info Session Feb 2021 FINAL FR.pdf
- 15:44, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page SCinstrmed (Content added) Tag: Visual edit
- 15:07, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:HC medical device FRN Form FINAL 2021-05-28.pdf (This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations.)
- 15:07, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:HC medical device FRN Form FINAL 2021-05-28.pdf (This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations.)
- 15:05, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Questions and Answers FRN FINAL EN.pdf (A questions & answers document was prepared in response to enquiries received related to the implementation of foreign risk notification (FRN).)
- 15:05, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Questions and Answers FRN FINAL EN.pdf (A questions & answers document was prepared in response to enquiries received related to the implementation of foreign risk notification (FRN).)
- 15:04, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Deck Info Session Feb 2021 FINAL EN.pdf (Information sessions were offered by Health Canada in February 2021 on the new post-market regulations. The presentation slide deck is available.)
- 15:04, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Deck Info Session Feb 2021 FINAL EN.pdf (Information sessions were offered by Health Canada in February 2021 on the new post-market regulations. The presentation slide deck is available.)
- 14:40, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page HCmeddev (New page) Tag: Visual edit
- 14:23, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Guidance document links Post-Market FINAL FR.pdf (Quatre ensembles de lignes directrices sont disponibles pour appuyer l'interprétation des dispositions post-commercialisation nouvelles ou mises à jour du Règlement sur les instruments médicaux qui ont été publiées dans la Gazette du Canada Partie II le 23 décembre 2020.)
- 14:23, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Guidance document links Post-Market FINAL FR.pdf (Quatre ensembles de lignes directrices sont disponibles pour appuyer l'interprétation des dispositions post-commercialisation nouvelles ou mises à jour du Règlement sur les instruments médicaux qui ont été publiées dans la Gazette du Canada Partie II le 23 décembre 2020.)
- 14:20, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs created page File:Guidance document links Post-Market FINAL EN.pdf (Four guidance documents are available to support the interpretation of the new or updated post-market provisions in the Medical Devices Regulations that were published in Canada Gazette Part II on December 23, 2020.)
- 14:20, 1 June 2021 Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs uploaded File:Guidance document links Post-Market FINAL EN.pdf (Four guidance documents are available to support the interpretation of the new or updated post-market provisions in the Medical Devices Regulations that were published in Canada Gazette Part II on December 23, 2020.)
- 13:57, 1 June 2021 User account Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs was created automatically