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Domain Informations
Reghelps.com lookup results from whois.godaddy.com server:
- Domain created: 2019-08-02T07:49:00Z
- Domain updated: 2023-08-03T09:25:06Z
- Domain expires: 2025-08-02T07:49:00Z 1 Year, 17 Days left
- Website age: 4 Years, 348 Days
- Registrar Domain ID: 2419298087_DOMAIN_COM-VRSN
- Registrar Url: http://www.godaddy.com
- Registrar WHOIS Server: whois.godaddy.com
- Registrar Abuse Contact Email: [email protected]
- Registrar Abuse Contact Phone: 480-624-2505
- Name server:
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- NS34.DOMAINCONTROL.COM
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Host Informations
Host name | 200.7.205.92.host.secureserver.net |
IP address | 92.205.7.200 |
Location | Germany |
Latitude | 51.4476 |
Longitude | 7.0122 |
Timezone | Europe/Berlin |
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REGHELPS admineu 2022-11-23T11:58:26+00:00. WHO WE ARE. REGHELPS is a global medical device regulatory consultancy firm that also serves as a European Authorized …
Reghelps.comDA: 16 PA: 16 MOZ Rank: 17
US FDA Registration Consultants – No. 1 FDA Expert
As an FDA Consultants team, REGHELPS is made up of a powerful combination of compliance, regulatory, scientific, and technical experts who are very good at solving and …
Reghelps.comDA: 16 PA: 27 MOZ Rank: 44
Best FDA Consultants and US Agents in Europe
We, US FDA Consultants and US Agents serve in the areas of FDA related GMP, 510k, product approvals, and establishment registrations through our long-standing mastery of …
Reghelps.comDA: 16 PA: 8 MOZ Rank: 26
Technical File & MDR Technical Documentation for …
ISO 14971: 2019 Medical devices – Application of risk management to medical devices contains risk management guidelines. In addition, the requirements stated in Chapter 1 …
Reghelps.comDA: 16 PA: 35 MOZ Rank: 54
Single Registration Number MDR – An Overview
Jul 2, 2021 The Single Registration Number (SRN) is a unique code that is used to identify an economic operator in the EU without ambiguity. The SRN number is generated by EUDAMEDand issued by the competent …
Reghelps.comDA: 16 PA: 32 MOZ Rank: 52
510k Submission Process– RegHelps - HackMD
Feb 22, 2023 # 510k Submission Process– RegHelps Note: If you plan to market a new medical device in the United Danial Michil Linked with GitHub
Hackmd.ioDA: 9 PA: 34 MOZ Rank: 48
MDR Classification & IVDR Classification Guide
TECHNICAL DOCUMENTATION EUROPEAN AUTHORISED REPRESENTATIVE CLINICAL EVALUATION REPORT MEDICAL DEVICE RISK MANAGEMENT – ISO …
Reghelps.comDA: 16 PA: 34 MOZ Rank: 56
reghelps Publisher Publications - Issuu
Reghelps DE. We work as a single united team with market-leading firms around the world and give our clients the highest quality advice possible.
Issuu.comDA: 9 PA: 9 MOZ Rank: 25
RegList - Home Page
WELCOME TO REGLIST! The RegList membership website provides members with exclusive member-only content, including discounted event registration, an industry resource center, ability to view & post job …
Reglist.orgDA: 11 PA: 11 MOZ Rank: 20
510k Consultants
At RegHelps, we provide Clinical Evaluation Report Writing and Clinical Investigation Service. Contact us for genuine service in line with article 61 and MEDDEV 2.7.1 Rev 4 …
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REGhelps - Overview - Trepup
REGhelps help organizations to overcome regulatory hurdles of CE marking & FDA by sharing,guiding,training & developing documents that of high quality,economically viable …
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Oct 29, 2019 Self-Reg Foundations Certificate Program. Our flagship Self-Reg Foundations Certificate Program has been a game-changer for thousands of learners, …
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Clinical Evaluation and Its Process - RegHelps - Issuu
Nov 25, 2022 At RegHelps, we provide Clinical Evaluation Report Writing and Clinical Investigation Service. Contact us for genuine service in line with article 61 and MEDDEV …
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I3CGLOBAL REGHELPS PRIVATE LIMITED Company Profile
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Technical Documentation Support Service Professional - Issuu
The Medical Device Regulation (MDR) continues this approach with the "general safety and performance requirements", also in Annex I.
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