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
-
浅析体外诊断试剂成品检验及留样检验的若干要求
2024-05-21 115 -
浅谈螺杆桩螺纹段长度对承载力的影响
2024-05-21 85 -
溶解细菌纤维素的方法VIP免费
2024-05-21 92 -
Box-Cox变换及其在STATA软件中的实现VIP免费
2024-07-10 110 -
IEC60601-1-2_...电放电抗扰度测试变化及对策VIP免费
2025-04-12 71 -
9.2025年版《中国药典》四部理化分析通用技术要求增修订概况
2025-04-12 56 -
8.2025年版《中国药典》（四部）通用技术要求和指导原则增修订概况
2025-04-12 92 -
7.2025年版《中国药典》三部通则0237国家生物标准物质研制解读
2025-04-12 103 -
6.2025年版《中国药典》三部关于异常毒性检查修订内容的解读
2025-04-12 81 -
医疗器械注册资料技术审评探讨VIP免费
2025-09-16 79
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
