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Malware Scan Info
Macafee Check :
Email address with qadvis.com
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Domain Informations
Qadvis.com lookup results from whois.ascio.com server:
- Domain created: 2013-09-09T08:22:25Z
- Domain updated: 2023-07-26T09:36:01Z
- Domain expires: 2024-09-09T08:22:25Z 0 Years, 102 Days left
- Website age: 10 Years, 262 Days
- Registrar Domain ID: 1826597296_DOMAIN_COM-VRSN
- Registrar Url: http://www.ascio.com
- Registrar WHOIS Server: whois.ascio.com
- Registrar Abuse Contact Email: [email protected]
- Registrar Abuse Contact Phone: +1.4165350123
- Name server:
- NS1.BDM.MICROSOFTONLINE.COM
- NS2.BDM.MICROSOFTONLINE.COM
Network
- inetnum : 104.146.0.0 - 104.147.255.255
- name : O365
- handle : NET-104-146-0-0-1
- status : Direct Allocation
- created : 2014-06-06
- changed : 2024-03-18
- desc : To report suspected security issues specific to traffic emanating from Microsoft online services, including the distribution of malicious content or other illicit or illegal material through a Microsoft online service, please submit reports to:,* https://cert.microsoft.com.,For SPAM and other abuse issues, such as Microsoft Accounts, please contact:,* [email protected].,To report security vulnerabilities in Microsoft products and services, please contact:,* [email protected].,For legal and law enforcement-related requests, please contact:,* [email protected],For routing, peering or DNS issues, please,contact:,* [email protected]
Owner
- organization : Microsoft Corporation
- handle : MC-790
- address : Array,Redmond,WA,98052,US
Technical support
- handle : KIMAV-ARIN
- name : Kim, Avery
- phone : +1-425-882-8080
- email : [email protected]
Abuse
- handle : MAC74-ARIN
- name : Microsoft Abuse Contact
- phone : +1-425-882-8080
- email : [email protected]
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Host Informations
Host name | 104.146.132.36 |
IP address | 104.146.132.36 |
Location | Dublin Ireland |
Latitude | 53.3338 |
Longitude | -6.2488 |
Timezone | Europe/Dublin |
Postal | D02 |
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Site Inspections
Websites Listing
We found Websites Listing below when search with qadvis.com on Search Engine
QAdvis - Home - Facebook
QAdvis is based in Sweden with two offices, Lund and Stockholm. We are 20 senior and expert... Färögatan 33, 7th floor, 164 53 Stockholm, Sweden
Facebook.comDA: 16 PA: 8 MOZ Rank: 24
QAdvis AB | LinkedIn
QAdvis AB is a longtime trusted service provider for the medical device and in vitro diagnostic device industry. We offer a complete range of multidisciplinary services within …
Linkedin.comDA: 16 PA: 15 MOZ Rank: 32
QAdvis IVDR breakfast seminar - YouTube
QAdvis free seminar on In Vitro Device regulation (in Swedish).
Youtube.comDA: 15 PA: 6 MOZ Rank: 23
QAdvis (C) -10-2019 11 - Swedish Medtech
QAdvis. Make sure the following is clear and sufficient • EN ISO 14971 • Sufficient Risk Management team competences (Risk Management, technological, clinical, biocompatibility etc.) Risk Management • MEDDEV 2.7/1 Rev 4 • MDR Annex XIV and article 61 • Safety and performance • Meet all claims? Evaluation of clinical data • EN ISO 15223-1 • Use appropriate …
Swedishmedtech.seDA: 21 PA: 11 MOZ Rank: 35
QAdvis - Frukost Ready Set MDR 2017-11-16 - YouTube
Emma Axelsson och Maria Eklycke, QAdvis, pratar om hur övergången till MDR kommer att påverka den medicintekniska branschen.
Youtube.comDA: 15 PA: 6 MOZ Rank: 25
QADVIS UK LIMITED - GetTheData
QADVIS UK LIMITED is an active private limited company, incorporated on 4 November 2020. The nature of the business is Agents specialized in the sale of other particular products. The company's registered office is on Frederick Street, Edinburgh. The company's next accounts are due on 4 August 2022, and fall under the accounts category: No Accounts Filed.
Getthedata.comDA: 18 PA: 35 MOZ Rank: 58
El nuevo telefonillo inteligente - Fabricado en España
Descubre Qvadis. El nuevo telefonillo inteligente. Controla el acceso a tu casa o negocio. Sencillo, sin obras. Por fín, #DomóticaParaTodos, con #TecnologíaAccesible.
Qvadis.esDA: 13 PA: 13 MOZ Rank: 20
QAdvis | Medicon Village
QAdvis är ett konsultbolag som stödjer kunder, med medicintekniska och IVD produkter, genom hela den regulatoriska livscykelprocessen grundat i en djup kunskap och långvarig erfarenhet kring regelverk, standarder, guidelines samt kring effektiva arbetsmetoder och best practices...
Mediconvillage.seDA: 21 PA: 17 MOZ Rank: 45
欧盟授权的CE认证的机构有哪些? - 知乎
CE认证的2种认证类型:. 公告机构证书: 由欧盟公告机构(Notified Body简称NB)测试和出具的证书,企业无需签发《自我声明书》,由公告机构对产品符合性承担责任,受法律保护。. 因此,对于欧盟公告机构颁发的CE证书,不存在判定有效性的问题。. 对于产品 ...
Zhuanlan.zhihu.comDA: 18 PA: 12 MOZ Rank: 38
home - RMD2022
It is our pleasure to invite you to join us for The Virtual 6 th EAAR Annual Conference on New Medical Device Regulations (RMD2022).. At a time when digital communication is transforming every industry and every part of our daily life and work, we are committed to run an event that reaches as far as possible and fosters collaboration and …
Rmd2022.comDA: 11 PA: 11 MOZ Rank: 21
Medical Device Regulatory Compliance Experts | MedQtech
MedQtech is an experienced team of medical device regulatory and quality compliance specialists. We partner with medical device companies to ensure a streamlined journey to compliance and to drive quality enhancement throughout an organisation – ensuring compliance and quality systems are not barriers but enablers.
Medqtech.comDA: 12 PA: 12 MOZ Rank: 23
QAdvis AB - Företagsinformation - allabolag.se
QAdvis AB,556940-5045 - På allabolag.se hittar du , bokslut, nyckeltal, koncern, koncernträd, styrelse, Status, varumärken, adress mm för QAdvis AB
Allabolag.seDA: 16 PA: 21 MOZ Rank: 48
EnginZyme
Enabling the future of sustainable chemical production We are solving one of the fundamental challenges of our time – how to produce chemicals, foods, materials and other products that modern society relies on, in a truly sustainable way Explore
Enginzyme.comDA: 13 PA: 13 MOZ Rank: 26
QAdvis receive DI Gasell company 2021 award - Medicon Village
QAdvis receive DI Gasell company 2021 award. QAdvis. Publicerad 16 november 2021 - 1 min lästid. This is great fun and we are very honored and proud! We are so grateful to our clients, our team and of course Dagens Industri. The Gasell business requirements to be met extend over a three-year period and need to be achieved by organic growth. We have …
Mediconvillage.seDA: 21 PA: 47 MOZ Rank: 81
Robert Ginsberg, Co-founder and ceo at Qadvis | SlideShare
Robert Ginsberg Embed. Embed this SlideShelf. Choose an embed size: 490×470 615×470 760×570. Copy and paste this code into your blog or website: Copy. Copied ×.
Slideshare.netDA: 18 PA: 15 MOZ Rank: 47
TIES TEST – Horizon 2020 EU Fast Track to Innovation
QAdvis. A MedTech Consulting company within Quality, Regulatory & Clinical Evaluations. QAdvis. Accelerating Surgical Technologies. 3D Systems. Providing 3D Printing technology and Medical Device Healthcare solutions. 3D Systems. Horizon 2020: Agreement. Grant Agreement number: 831144 Action acronym: TIES-TEST . Horizon 2020 : Action Title. Action title: …
Ties-test.euDA: 12 PA: 12 MOZ Rank: 28
Medical Software Regulation and Compliance (EU MDR 2017/745)...
This training day was first arranged in co-operation with USBIMED and QAdvis AB at May 2018. As a response to requests this succesfull training day will be arranged again since a lot is happening at the moment, what comes to regulations and software at EU and also globally. Content is updated and represents current knowhow with future perspective also. AIM OF THE …
Upgraded.fiDA: 15 PA: 50 MOZ Rank: 34
Robert Ginsberg Archives - RMD2022
Robert Ginsberg is co-founder and Chairman of the Board of QAdvis, a Sweden based consulting company in medical device regulations. He specializes in software regulatory issues relating to medical devices and modern software engineering methods, tools and technologies, for example agile methods, continual deployment or artificial intelligence.
Rmd2022.comDA: 11 PA: 35 MOZ Rank: 63
Lumito anlitar QAdvis och startar arbetet mot CE-märkning
Bolaget har därför påbörjat aktiviteterna för att implementera sitt kvalitetssystem och för framtagande av teknisk fil som grund för CE-märkning. Arbetet sker i nära samarbete med Lumitos utvecklingspartner TTP och med QAdvis inom det regulatoriska området. Målsättningen är att ha den första produkten CE-märkt under Q1 2020.
News.cision.comDA: 15 PA: 50 MOZ Rank: 32
Crash Course UDI » GS1 Sweden
I den här kursen ger vi dig kunskap, tips och råd för att komma igång med att märka dina produkter med UDI.. UDI (Unique Device Identification) är en metod för att märka och identifiera medicinsk utrustning. Metoden ger en globalt unik identifiering i både distribution och användning, och ökar därmed spårbarheten för produkten.
Gs1.seDA: 6 PA: 26 MOZ Rank: 51
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