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Nibbler tested a sample of 5 pages from this website at 10:36 AM on Apr 18, 2024 (BST).
0% of pages are optimized for printing
Page | |
www.qservegroup.com/ | Not detected |
www.qservegroup.com/eu/en/home | Not detected |
www.qservegroup.com/eu/.../services | Not detected |
www.qservegroup.com/eu/.../market-access | Not detected |
www.qservegroup.com/eu/.../expertise | Not detected |
URL | Heading | Level |
www.qservegroup.com/ | Medical Device consultancy | H2 |
www.qservegroup.com/ | IVD Consultancy | H2 |
www.qservegroup.com/ | Market Access | H2 |
www.qservegroup.com/ | Medical Device CRO | H2 |
www.qservegroup.com/ | Webinars & Events | H2 |
www.qservegroup.com/ | Knowledge Center | H2 |
www.qservegroup.com/ | Your Global MedTech Partner for Regulatory Affairs, Quality Assurance and Clinical Trials | H2 |
www.qservegroup.com/ | Why choose Qserve as your regulatory consultant? | H2 |
www.qservegroup.com/ | News | H2 |
www.qservegroup.com/ | Events | H2 |
www.qservegroup.com/ | Newsletter | H2 |
www.qservegroup.com/ | Qserve Consultancy B.V. - HQ | H2 |
www.qservegroup.com/ | Newsletter | H2 |
www.qservegroup.com/ | Qserve is the largest consultant company in the EU that is 100% focused on medical devices and in-vitro diagnostics. Check out our company video. | H3 |
www.qservegroup.com/ | FAQ Questions | H3 |
www.qservegroup.com/ | On-demand Webinars | H3 |
www.qservegroup.com/ | Our method | H3 |
www.qservegroup.com/ | The Role of Biological Risk Management in Medical Device Development | H3 |
www.qservegroup.com/ | Countdown to Compliance: Safeguarding Your EU Market Access in Less Than 100 Days – Stay on Track! | H3 |
www.qservegroup.com/ | Online Training | A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK | H3 |
www.qservegroup.com/ | Virtual Training | FDA Approval Process for Medical Devices | H3 |
www.qservegroup.com/ | Free Webinar | EU-IVDR two years on. Understanding and effectively using the IVDR transition for successful CE marking | H3 |
www.qservegroup.com/eu/en/home | Medical Device consultancy | H2 |
www.qservegroup.com/eu/en/home | IVD Consultancy | H2 |
www.qservegroup.com/eu/en/home | Market Access | H2 |
www.qservegroup.com/eu/en/home | Medical Device CRO | H2 |
www.qservegroup.com/eu/en/home | Webinars & Events | H2 |
www.qservegroup.com/eu/en/home | Knowledge Center | H2 |
www.qservegroup.com/eu/en/home | Your Global MedTech Partner for Regulatory Affairs, Quality Assurance and Clinical Trials | H2 |
www.qservegroup.com/eu/en/home | Why choose Qserve as your regulatory consultant? | H2 |
www.qservegroup.com/eu/en/home | News | H2 |
www.qservegroup.com/eu/en/home | Events | H2 |
www.qservegroup.com/eu/en/home | Newsletter | H2 |
www.qservegroup.com/eu/en/home | Qserve Consultancy B.V. - HQ | H2 |
www.qservegroup.com/eu/en/home | Newsletter | H2 |
www.qservegroup.com/eu/en/home | Qserve is the largest consultant company in the EU that is 100% focused on medical devices and in-vitro diagnostics. Check out our company video. | H3 |
www.qservegroup.com/eu/en/home | FAQ Questions | H3 |
www.qservegroup.com/eu/en/home | On-demand Webinars | H3 |
www.qservegroup.com/eu/en/home | Our method | H3 |
www.qservegroup.com/eu/en/home | The Role of Biological Risk Management in Medical Device Development | H3 |
www.qservegroup.com/eu/en/home | Countdown to Compliance: Safeguarding Your EU Market Access in Less Than 100 Days – Stay on Track! | H3 |
www.qservegroup.com/eu/en/home | Online Training | A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK | H3 |
www.qservegroup.com/eu/en/home | Virtual Training | FDA Approval Process for Medical Devices | H3 |
www.qservegroup.com/eu/en/home | Free Webinar | EU-IVDR two years on. Understanding and effectively using the IVDR transition for successful CE marking | H3 |
www.qservegroup.com/eu/.../services | Medical device and IVD consulting services | H1 |
www.qservegroup.com/eu/.../services | Consulting services | H2 |
www.qservegroup.com/eu/.../services | Regulatory consulting for medical device and IVD companies | H2 |
www.qservegroup.com/eu/.../services | Clinical evaluation or clinical studies | H2 |
www.qservegroup.com/eu/.../services | Quality Assurance- ISO 13485 -QMS for medical devices | H2 |
www.qservegroup.com/eu/.../services | Regulatory, Quality and Clinical Training | H2 |
www.qservegroup.com/eu/.../services | Stay up to date with the latest updates from Qserve | H2 |
www.qservegroup.com/eu/.../services | Newsletter | H2 |
www.qservegroup.com/eu/.../services | Qserve Consultancy B.V. - HQ | H2 |
www.qservegroup.com/eu/.../services | Newsletter | H2 |
www.qservegroup.com/eu/.../services | Some of our regulatory services: | H3 |
www.qservegroup.com/eu/.../services | Some of our clinical services for medical devices: | H3 |
www.qservegroup.com/eu/.../services | Some of our Quality Assurance services: | H3 |
www.qservegroup.com/eu/.../services | Some of our training opportunities: | H3 |
www.qservegroup.com/eu/.../services | Regulatory Affairs | H3 |
www.qservegroup.com/eu/.../services | Regulatory consulting for device and IVD companies | H3 |
www.qservegroup.com/eu/.../services | Clinical Affairs | H3 |
www.qservegroup.com/eu/.../services | Clinical Evaluation (CER) or Clinical Studies | H3 |
www.qservegroup.com/eu/.../services | Quality Assurance | H3 |
www.qservegroup.com/eu/.../services | ISO 13485 - QMS for Medical Devices | H3 |
www.qservegroup.com/eu/.../services | Training Academy | H3 |
www.qservegroup.com/eu/.../services | Regulatory, Quality and Clinical Training | H3 |
www.qservegroup.com/eu/.../services | We share regulatory news | H3 |
www.qservegroup.com/eu/.../services | Meet and Greet Qserve experts | H3 |
www.qservegroup.com/eu/.../services | Join our growing team of experts | H3 |
www.qservegroup.com/eu/.../services | Follow us on LinkedIn | H3 |
www.qservegroup.com/eu/.../market-access | Global Regulatory Market Access Medical Devices and IVDs | H1 |
www.qservegroup.com/eu/.../market-access | Navigating Market Approvals for Medical Devices and IVDs | H2 |
www.qservegroup.com/eu/.../market-access | Why Choose Qserve for your Global Market Access? | H2 |
www.qservegroup.com/eu/.../market-access | Stay up to date with the latest updates from Qserve | H2 |
www.qservegroup.com/eu/.../market-access | Newsletter | H2 |
www.qservegroup.com/eu/.../market-access | Qserve Consultancy B.V. - HQ | H2 |
www.qservegroup.com/eu/.../market-access | Newsletter | H2 |
www.qservegroup.com/eu/.../market-access | United States | H3 |
www.qservegroup.com/eu/.../market-access | Europe | H3 |
www.qservegroup.com/eu/.../market-access | United Kingdom (UK) | H3 |
www.qservegroup.com/eu/.../market-access | Switzerland (CH) | H3 |
www.qservegroup.com/eu/.../market-access | China | H3 |
www.qservegroup.com/eu/.../market-access | Global Medical Device Registration | H3 |
www.qservegroup.com/eu/.../market-access | Contact us today to begin your journey toward successful global medical device registration with Qserve. | H3 |
www.qservegroup.com/eu/.../market-access | We share regulatory news | H3 |
www.qservegroup.com/eu/.../market-access | Meet and Greet Qserve experts | H3 |
www.qservegroup.com/eu/.../market-access | Join our growing team of experts | H3 |
www.qservegroup.com/eu/.../market-access | Follow us on LinkedIn | H3 |
www.qservegroup.com/eu/.../expertise | Expertise | H1 |
www.qservegroup.com/eu/.../expertise | Newsletter | H2 |
www.qservegroup.com/eu/.../expertise | Qserve Consultancy B.V. - HQ | H2 |
www.qservegroup.com/eu/.../expertise | Newsletter | H2 |
www.qservegroup.com/eu/.../expertise | Our technical experts hold over 70 graduate degrees. | H3 |
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Compression
Link URL | Link text | Page URL |
www.qservegroup.com/.../the-role-of-biological-risk-management-in-medical-device-development | Blog April 02, 2024 The Role of Biological Risk Management in Medical Device Development The biological evaluation of medical devices, guided by ISO standards, must be integrated into the risk management process to ensure comprehensive consideration of biological risks, a task often challenging for manufacturers but addressed by Qserve through expert collaboration, structured assessment, and data integration for enhanced safety evaluation and testing. | www.qservegroup.com/ |
www.qservegroup.com/.../countdown-to-compliance--safeguarding-your-eu-market-access-in-less-than-100-days--stay-on-track | Blog March 06, 2024 Countdown to Compliance: Safeguarding Your EU Market Access in Less Than 100 Days – Stay on Track! As the May 26, 2024, deadline for EU MDR transition approaches, regulatory compliance becomes paramount. | www.qservegroup.com/ |
www.qservegroup.com/.../online-training--a-regulatory-update-on-the-medical-device-and-in-vitro-diagnostic-regulations-in-the-eu-and-uk | Training April 30, 2024 - April 30, 2024 / Europe Online Training | A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK In this live online training our IVD expert Sue Spencer, together with three other presenters provide the latest developments on the MDR and IVDR in the European Union and the recent medical device regulatory developments in the UK, organised by Management Forum. | www.qservegroup.com/ |
www.qservegroup.com/.../free-webinar--eu-ivdr-two-years-onpunt-understanding-and-effectively-using-the-ivdr-transition-for-successful-ce-marking | Webinar May 28, 2024 - May 28, 2024 / Europe Free Webinar | EU-IVDR two years on. Understanding and effectively using the IVDR transition for successful CE marking | www.qservegroup.com/ |
www.qservegroup.com/.../the-role-of-biological-risk-management-in-medical-device-development | Blog April 02, 2024 The Role of Biological Risk Management in Medical Device Development The biological evaluation of medical devices, guided by ISO standards, must be integrated into the risk management process to ensure comprehensive consideration of biological risks, a task often challenging for manufacturers but addressed by Qserve through expert collaboration, structured assessment, and data integration for enhanced safety evaluation and testing. | www.qservegroup.com/eu/en/home |
www.qservegroup.com/.../countdown-to-compliance--safeguarding-your-eu-market-access-in-less-than-100-days--stay-on-track | Blog March 06, 2024 Countdown to Compliance: Safeguarding Your EU Market Access in Less Than 100 Days – Stay on Track! As the May 26, 2024, deadline for EU MDR transition approaches, regulatory compliance becomes paramount. | www.qservegroup.com/eu/en/home |
www.qservegroup.com/.../online-training--a-regulatory-update-on-the-medical-device-and-in-vitro-diagnostic-regulations-in-the-eu-and-uk | Training April 30, 2024 - April 30, 2024 / Europe Online Training | A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK In this live online training our IVD expert Sue Spencer, together with three other presenters provide the latest developments on the MDR and IVDR in the European Union and the recent medical device regulatory developments in the UK, organised by Management Forum. | www.qservegroup.com/eu/en/home |
www.qservegroup.com/.../free-webinar--eu-ivdr-two-years-onpunt-understanding-and-effectively-using-the-ivdr-transition-for-successful-ce-marking | Webinar May 28, 2024 - May 28, 2024 / Europe Free Webinar | EU-IVDR two years on. Understanding and effectively using the IVDR transition for successful CE marking | www.qservegroup.com/eu/en/home |
Rendering Chart...
Page | Characters | Words |
www.qservegroup.com/ | 5054 | 672 |
www.qservegroup.com/eu/en/home | 5054 | 672 |
www.qservegroup.com/eu/.../services | 4785 | 691 |
www.qservegroup.com/eu/.../market-access | 6081 | 833 |
www.qservegroup.com/eu/.../expertise | 5375 | 719 |
5% of images have a clearly defined size
7 images are being resized by the browser
100% of pages use analytics
Google Tag Manager
100% of pages have defined titles
0% of page titles are weak
This is how this website will look in Google search listings:
Qserve | Your Global MedTech Partner for Regulatory Affairs, Quality ...
www.qservegroup.com/
Qserve is your MedTech Consultant for Regulatory Affairs & Quality Assurance and Clinical Trials. Need regulatory advice, support or training? Contact us.
Page URL | Name | Content |
www.qservegroup.com/ | description | Qserve is your MedTech Consultant for Regulatory Affairs & Quality Assurance and Clinical Trials. Need regulatory advice, support or training? Contact us. |
www.qservegroup.com/ | title | Global Market Access for Medical Devices - Qserve Group |
www.qservegroup.com/ | author | AGN Business Internet BV |
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www.qservegroup.com/eu/en/home | description | Qserve is your MedTech Consultant for Regulatory Affairs & Quality Assurance and Clinical Trials. Need regulatory advice, support or training? Contact us. |
www.qservegroup.com/eu/en/home | title | Global Market Access for Medical Devices - Qserve Group |
www.qservegroup.com/eu/en/home | author | AGN Business Internet BV |
www.qservegroup.com/eu/en/home | viewport | width=device-width, initial-scale=1 |
www.qservegroup.com/eu/.../services | description | Working with a global team of experts, Qserve has managed a diverse array of projects in the medical device industry. Together, we bring your medical device to the global market. Contact us |
www.qservegroup.com/eu/.../services | title | Qserve l You global Partner for Medical Device market access consulting |
www.qservegroup.com/eu/.../services | author | AGN Business Internet BV |
www.qservegroup.com/eu/.../services | viewport | width=device-width, initial-scale=1 |
www.qservegroup.com/eu/.../market-access | description | We support worldwide manufacturers with market access medical devices and in vitro diagnostics specializing in Regulatory, Quality Affairs, Clinical Trials, and Training. |
www.qservegroup.com/eu/.../market-access | title | Global Regulatory Market Access Medical Devices and IVDs |
www.qservegroup.com/eu/.../market-access | author | AGN Business Internet BV |
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www.qservegroup.com/eu/.../expertise | description | qservegroup |
www.qservegroup.com/eu/.../expertise | title | Expertise |
www.qservegroup.com/eu/.../expertise | author | The Qserve Group |
www.qservegroup.com/eu/.../expertise | viewport | width=device-width, initial-scale=1 |
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www.qservegroup.com/ | X-UA-Compatible | IE=edge,chrome=1 |
www.qservegroup.com/ | language | NL |
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Every URL is well written
Last updated April 2, 2024
Date | File | Source |
4/2/24 | www.qservegroup.com/ | Body text |
3/6/24 | www.qservegroup.com/ | Body text |
4/2/24 | www.qservegroup.com/eu/en/home | Body text |
3/6/24 | www.qservegroup.com/eu/en/home | Body text |
5/26/21 | www.qservegroup.com/eu/.../market-access | Body text |
10/3/22 | www.qservegroup.com/.../LinkedIn.min.png | Last modified header |
10/3/22 | www.qservegroup.com/.../Vacatures.min.jpg | Last modified header |
10/3/22 | www.qservegroup.com/.../Events.min.jpg | Last modified header |
10/3/22 | www.qservegroup.com/img/.../Knowledge | Last modified header |
10/3/22 | www.qservegroup.com/img/logo_white.png | Last modified header |
10/3/22 | www.qservegroup.com/.../WeChat-Image-Qserve.jpg | Last modified header |
10/3/22 | www.qservegroup.com/.../Wechat-logo.png | Last modified header |
10/3/22 | www.qservegroup.com/.../qserve-pand.jpg | Last modified header |
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10/3/22 | www.qservegroup.com/.../globalregistration.png | Last modified header |
3/27/23 | www.qservegroup.com/img/logo-25years-b.png | Last modified header |
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