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Medcert | MEDCERT ist Spezialist für die Zertifizierung von Medizinprodukten und QM-Systemen im Medizinbereich. Als eine der größten Benannten Stellen Deutschlands bieten wir außer CE-Kennzeichnung auch internationale Zulassungen für Medizinprodukte an.

Medcert | MEDCERT ist Spezialist für die Zertifizierung von Medizinprodukten und QM-Systemen im Medizinbereich. Als eine der größten Benannten Stellen Deutschlands bieten wir außer CE-Kennzeichnung auch internationale Zulassungen für Medizinprodukte an.

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med-cert.com
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ce-certification.us

ce-certification.us ce-certification.us           
CE Certification - Medical Device CE Marking
CE Marking, also referred as CE Mark is a legal requirement for medical devices (medical equipments) to market in the Europe. CE Marking (CE Mark) is recognized worldwide as a symbol of quality.


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lne-gmed.com

lne-gmed.com lne-gmed.com           
GMED - Dedicated to Health and Innovation in Medical Devices
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eumdr.com

eumdr.com eumdr.com           
The European Union Medical Device Regulation - Regulation (EU) 2017/745 (EU MDR)
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obelis.net

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lne-america.com

lne-america.com lne-america.com           
GMED - Dedicated to Health and Innovation in Medical Devices
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ce-marking.com

ce-marking.com ce-marking.com           
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World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.


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orielstat.com

orielstat.com orielstat.com           
Oriel STAT A MATRIX | Medical Device Training, Consulting & Audits
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medical-device-regulation.eu

medical-device-regulation.eu medical-device-regulation.eu           
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mdi-europa.com

mdi-europa.com mdi-europa.com           
mdi Europa | CE Marking "Made in Germany" for Medical Devices
Germany based EU Authorized Representative "mdi Europa" helps small to medium sized manufacturers to enter european medical device market.


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cemarkingassociation.co.uk

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CE Marking Testing & Compliance UK - Contact Specialists Now
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i3cglobal.com

i3cglobal.com i3cglobal.com           
World-Class Medical Device Regulatory Consulting Services
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thema-med.com

thema-med.com thema-med.com           
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Servizi di consulenza strategico-regolatoria per aziende che operano nel settore dei Dispositivi Medici, dei Dispositivi Medico-Diagnostici in Vitro...


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nbog.eu nbog.eu           
NBOG - Start
ZLG, Bonn



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decomplix.com

decomplix.com decomplix.com           
We Simplify Market Access for Medical Devices - Decomplix
Ensure 100% medical compliance. Decomplix does your CE certification for medical devices and IVD in the pre- and post-market phase. Learn more here.


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johner-institute.com

johner-institute.com johner-institute.com           
Johner Institute - your regulatory partner
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regulatorypharmanet.com regulatorypharmanet.com           
Regulatory Pharma Net
Regulatory Pharma Net (RPN), founded in 1999, is a qualified Regulatory Affairs service and consulting company based in Italy. RPN highly-qualified team includes Regulatory Affairs, DrugDevelopment, Market Access and Pharmacovigilance Experts. RPN gives support during development, registration, launch and life cyclemanagement of Medicinal Products, Medical Devices, Cosmetics,Biocides and Food Supplements. RPN is partner of many pharmaceutical companies, managing hundredsof multitask projects, on a worldwide scale. We are proudly part of Pharos Healthcare Consulting, a new European Network of highly-specialised Market Access Strategic Consultancy. While maintaining each company’s independence and high local knowledge, we will be able to support Pharmaceutical companies in launching new drugs through our coordinated Market Access network across Europe, find out more at www.pharos-healthcare-consulting.com


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ce-mark.com ce-mark.com           
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Certification Experts
Product compliance made easier


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mdss.com

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EU Authorized Representative Services For Medical Devices
MDSS USA is a EU Authorized Representative for Medical Devices, CE Mark, MDD, IVDD, AIMDD and European regulatory affairs.
Family of CP/M- and DOS-compatible multi-user multi-tasking operating systems. Multiuser DOS is a real-time multi-user multi-tasking operating system for IBM PC-compatible microcomputers. An evolution of the older Concurrent CP/M-86, Concurrent DOS and Concurrent DOS 386 operating systems, it was originally developed by Digital Research and acquired and further developed by Novell in 1991. Its ancestry lies in the earlier Digital Research 8-bit operating systems CP/M and MP/M, and the 16-bit single-tasking CP/M-86 which evolved from CP/M. When Novell abandoned Multiuser DOS in 1992, the three master value-added resellers (VARs) DataPac Australasia, Concurrent Controls and Intelligent Micro Software were allowed to take over and continued independent development into Datapac Multiuser DOS and System Manager, CCI Multiuser DOS, and IMS Multiuser DOS and REAL/32.The FlexOS line, which evolved from Concurrent DOS 286 and Concurrent DOS 68K, was sold off to Integrated Systems, Inc. (ISI) in July 1994.


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conformance.co.uk

conformance.co.uk conformance.co.uk           
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We provide advice on UKCA and CE Marking Compliance for a range of industries including machinery. Self Assessment help and training.



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medcert.de

medcert.de medcert.de           
Medcert | MEDCERT ist Spezialist für die Zertifizierung von Medizinprodukten und QM-Systemen im Medizinbereich. Als eine der größten Benannten Stellen Deutschlands bieten wir außer CE-Kennzeichnung auch internationale Zulassungen für Medizinprodukte an.



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medicaldeviceslegal.com

medicaldeviceslegal.com medicaldeviceslegal.com           
medicaldeviceslegal | Medical devices legal and regulatory blog
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Emergo by UL is a leading regulatory consulting firm specializing in global medical device and IVD compliance. Our comprehensive solution is designed to help you achieve and maintain regulatory and commercial success.


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massmedic.com

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MassMEDIC - The Heart of HealthTech
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medicaldeviceacademy.com

medicaldeviceacademy.com medicaldeviceacademy.com           
Medical device consulting services Medical Device Academy
Are you a start-up device company that needs medical device consulting services and training for an FDA 510k submission?


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RegDesk offers an AI-powered medical devices and pharmaceutical regulatory compliance software to keep track of medical regulations. Click here to learn more!



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team-nb.org team-nb.org           
Bienvenue sur la page d'accueil
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The world's only 100% medical device-focused, full development Contract Research Organization (CRO). Learn how to accelerate your development program today!


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Medical Device consulting services - regulatory and quality - FDA, CE marking, ISO 13485, MDSAP, biological and clinical evaluation.


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crosscare.eu crosscare.eu           
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MDR & IVDR EU Conference 2020 • MDR & IVDR EU Regulation Training
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