fees-review-medical-device-licence-applications-2019-document-eng 医疗器械许可证申请审查费用 加拿大
VIP免费
Health Santé
Canada Canada
Guidance Document
Fees for the Review of Medical Device
Licence Applications
Date adopted: 1997/05/01
Date posted: 2019/11/04
Canada
Health Canada is responsible for helping Canadians maintain and improve their health.It
ensures that high-quality health services are accessible,and works to reduce health risks.
Egalement disponible en francais sous le titre:
Ligne directrice:Frais pour Pexamen des demandes d'homologation des instruments médicaux
To obtain additional information,please contact:
Health Canada
Address Locator 0900C2
Ottawa,Ontario K1A OK9
Tel.:613-957-2991
Toll free:1-866-225-0709
Fax:613-941-5366
TTY:1-800-465-7735
E-mail:hc.publications-publications.sc@canada.ca
Her Majesty the Queen in Right of Canada,as represented by the Minister of Health,2019
Publication date:November 2019
This publication may be reproduced for personal or internal use only without permission
provided the source is fully acknowledged.
Cat.:H13-9/20-2019E-PDF
ISBN:978-0-660-27439-3
Pub.:180196
Fees for the Review of Medical Device Licence Applications |2
Document change log
Version
Guidance Document:Fees for
the Review of Medical Device
Licence Applications
Replaces
Guidance Document:Fees
for the Review of Medical
Device Licence Applications
Date
April 1,2020(posted
November 4,2019)
Date
November 20,2015
Date
Change
Location
(Section,
paragraph)
Nature of and/or Reason
for change
April 1,2020
(posted
November 4,
2019)
Content was updated
All
As of April 1,2020,new
fees along with a revised
fee policy willcome into
force requiring significant
changes to the guidance
document
November
20,2015
Administrative Change
S.2.2.2
As of November 9th,2015,
the Accounts Receivable
address has changed
摘要:
展开>>
收起<<
HealthSantéCanadaCanadaGuidanceDocumentFeesfortheReviewofMedicalDeviceLicenceApplicationsDateadopted:1997/05/01Dateposted:2019/11/04CanadaHealthCanadaisresponsibleforhelpingCanadiansmaintainandimprovetheirhealth.Itensuresthathigh-qualityhealthservicesareaccessible,andworkstoreducehealthrisks.Egaleme...
声明:如果您的权利被侵害,请联系我们的进行举报。
相关推荐
-
ISO 14155-2020 医疗器械临床实验管理规范(中文版)VIP免费
2025-09-17 352 -
ISO 31000:2018 风险管理指南VIP免费
2025-10-28 303 -
ISO TS 10974-2018 评估有植入式医疗设备的患者进行磁共振成像的安全性VIP免费
2025-10-30 181 -
ISO TS 10974-2018 评估有植入式医疗设备的患者进行磁共振成像的安全性(中文版)
2025-10-30 240 -
ISO TS 10974-2018 评估有植入式医疗设备的患者进行磁共振成像的安全性_中英文版VIP专享
2025-10-30 141 -
ISO 10993-1-2018 医疗器械生物学评价 第1部分:风险管理过程中的评价与试验_中英文对照VIP专享
2025-11-03 152 -
ISO 14155-2026 人体医疗器械临床试验--良好临床实践VIP免费
2026-04-15 145 -
ISO IEC 17020 2026 Conformity assessment— Requirements for bodies performing inspectionVIP免费
2026-05-14 137 -
ISO 19011-2026-管理体系审核指南VIP免费
2026-06-03 110 -
ISO FDIS 9001_2026质量管理体系要求中英文版VIP免费
2026-07-02 364
作者:冒牌货
分类:专业资料
价格:60质量币
属性:15 页
大小:392.22KB
格式:PDF
时间:2026-01-08

