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Medical Devices | Material Biocompatibility | ISO 10993 |Medical Device Safety Complian... - 0 views

www.arazygroup.com/Biocompatibility

medical devices material biocompatibility ISO 10993 device safety compliance authorized representative FDA approval process

shared by arazy-group on 07 Jul 11 - No Cached
  • arazy-group on 07 Jul 11
     
    Arazy Group is a major global medical device consultant serving a number of medical developers and manufacturers by providing them with professional and specific knowledge and consulting services in launching their products at a global level.
  • arazy-group on 22 Sep 11
     
    Biocompatibility can be a complex process as many medical devices are made of more than one material. The current leading standard for biological evaluation of medical devices is ISO 10993 at its latest version.
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Medical Device Consultants in China | Medical Device Safety compliance - 0 views

arazygroup.com/blog

Safety compliance device medical consultants devices

shared by arazy-group on 20 Jul 11 - No Cached
  • arazy-group on 20 Jul 11
     
    Arazy Group offer international standard solution in achieving and surpassing the verification and validation norms of different medical device and health regulatory bodies in China.
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Medical Device Approval Japan | Medical Device Regulatory Vietnam - 0 views

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device medical devices consultants Safety compliance in Registration Equipment Experts

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Medical Device specific regulation strategy reports, Medical Device Registration with PMDA, Japan Health Technical documents Preparation, Japan Market Authorized Holder and local Representative (MAH), Japan GMP compliance and Arazy Group's unique line of GlobaR - Global Regulatory Hub™ products.
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Medical Device Consultants in Brazil | Medical Device Safety compliance - 0 views

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Safety compliance device medical consultants devices

shared by arazy-group on 19 Jul 11 - No Cached
  • arazy-group on 19 Jul 11
     
    Arazy Group offer expertise in medical device consultation and clinical literature review services in Brazil. We are the market leaders in gaining verification, validation and certification for different medical device manufacturers and marketers.
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Medical Device Consultants in Israel | Medical Device Safety compliance - 0 views

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Device Safety compliance medical consultants devices

shared by arazy-group on 19 Jul 11 - No Cached
  • arazy-group on 19 Jul 11
     
    Arazy Group offer quality and professional medical device registration services and work towards gaining validation, verification and market clearance for medical device and equipment manufacturers in Israel.
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Medical Device Registration Kuwait | Medical Device Consultants Kuwait - 0 views

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Medical Device Registration Kuwait Devices Consultants

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Gain medical device compliance and verification from medical device regulatory authorities in Kuwait with expert medical device consultancy services from us. Arazy Group is a global leader in medical device registration and offers a wide range of medical device regulation and clinical clearance services.
  • arazy-group on 26 Jul 11
     
    Gain medical device compliance and verification from medical device regulatory authorities in Kuwait with expert medical device consultancy services from us. Arazy Group is a global leader in medical device registration and offers a wide range of medical device regulation and clinical clearance services.
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Medical device registration Jordan | Medical Device Consultants Jordan - 0 views

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Medical registration Jordan Devices Device Consultants

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Gain compliance with the Ministry of Health (MOH) in Jordan for your medical products with the aid of world leading medical device consultants. Arazy Group helps you introduce and foray into the Jordanian market with your medical devices and equipment like no other medical device consultant.
  • arazy-group on 26 Jul 11
     
    Gain compliance with the Ministry of Health (MOH) in Jordan for your medical products with the aid of world leading medical device consultants. Arazy Group helps you introduce and foray into the Jordanian market with your medical devices and equipment like no other medical device consultant.
arazy-group

Sterilization Validation of Medical Devices | Medical Device Safety Compliance | Medica... - 0 views

www.arazygroup.com/Sterilizofedicalevices

sterilization validation of medical devices device safety compliance packaging process IVDD directive sterility assurance level FDA approval effective

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    Arazy Group offer complete third party lab services for medical device packaging and sterilization validation for any device and any risk classification.
  • arazy-group on 22 Sep 11
     
    Medical device manufacturers and distributors in the domestic as well as the international market is welcome to gain market approval and clearance for their medical devices and IVDs through the expert assistance of Arazy Group's incredible team of market experts, medical device industry analyzers, authorized representatives.
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Medical Device Reporting | Devices | Device Vigilance System | FDA Agent | Medical Devi... - 0 views

www.arazygroup.com/VigilanceReport

reporting devices system FDA agent regulatory registration GMP compliance listing Medical Device Vigilance

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    MDR procedure describing a system for the notification and evaluation of adverse incidents to be known as the Medical Devices Vigilance System.
  • arazy-group on 22 Sep 11
     
    Arazy Group offers a wide range of medical device consultations for fulfilling the different norms and specifications mandatory for medical device clearance and market entry all over the world.
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FDA US Agents | FDA Registration US | FDA Regulatory | Compliance FDA 510 | FDA US Agen... - 0 views

www.arazygroup.com/FDA-PMA

FDA US agents registration regulatory compliance FDA510 device listing FDA-PMA consulting consultin

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Arazy Group offers unique line of GlobaR - Global Regulatory Hub (Trade Mark) products such as GlobaR Dossier (Trade Mark), GlobaR - One World Process (Trade Mark), GlobaR Submission Center (Trade Mark) and Universal Authorized Representative (Trade Mark).
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Universal Authorized Representative | FDA Regulatory | Compliance FDA 510 | FDA US Agen... - 0 views

www.arazygroup.com/Univauthorep

universal authorized representative FDA regulatory compliance 510 US agents device listing european medical ISO 13485 design

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    European Union (EU) Authorized Representative, USA Designated agent, China after Sales service, Central & South American registrations holding companies, Japan MAH - Marketing Authorized Holder, Product Sponsor and similar entities are the legal and regulatory bodies a medical device manufacturer needs to source, appoint, contract, pay for and renew annually in order to fully satisfy the product sales clearance requirements.
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FDA 510 | FDA US Agents | FDA Device Listing | FDA US Agents | FDA Registration US | FD... - 0 views

www.arazygroup.com/FDA510KFilePreparation

FDA 510 US agents device listing registration regulatory compliance ISO 13485 and requirements

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Arazy Group help you with our expert CE Mark Consultancy services that offer verification, validation and product certification for medical devices, IVDs and equipment in Czech Republic. We also offer clinical trial monitoring and data management for you. You can gain from our numerous medical device regulatory and CE marking consulting services.
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Regulatory Dossier Preparation | Medical Device Safety Compliance | Medical Device Regu... - 0 views

www.arazygroup.com/EssentialRequirements

regulatory dossier preparation medical device safety compliance clinical trial data FDA US agents reporting registration and listing

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    A team of professional medical device regulatory and quality experts are here to assist you with writing, reviewing or editing of an "Essential Requirements" table, a complete CE technical file, a traditional 510k or a complicated PMA file.
arazy-group

Exhibitions | Medical Device Reporting | Devices | Device Vigilance System | FDA Agent ... - 0 views

www.arazygroup.com/Exhibitions

exhibitions reporting devices system FDA agent regulatory registration GMP compliance listing Medical Device Vigilance

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Arazy Group offers a wide range of medical device consultations for fulfilling the different norms and specifications mandatory for medical device clearance and market entry all over the world.
arazy-group

Medical Device , ANMAT GMP QMS System Implementation - 0 views

www.arazygroup.com/AnmatGMPQMS

Safety compliance device medical consultants devices

shared by arazy-group on 15 Jul 11 - No Cached
  • arazy-group on 15 Jul 11
     
    Any company that wants to manufacture or import medical devices in Argentina must have a Quality Management System in compliance with ANMAT's GMP. ANMAT GMP QMS System Implementation, Anmat GMP QMS System Implementation.
arazy-group

Medical Device Safety compliance, Medical Device Sterilization - 0 views

www.arazygroup.com/Sterilization

Safety compliance device medical consultants devices

shared by arazy-group on 07 Jul 11 - No Cached
  • arazy-group on 07 Jul 11
     
    Arazy Group is one of the leading medical device consultants that have been helping medical device companies in launching their products and equipment on a global level by carrying out medical device sterilization tests for them.
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Medical Device Consultants in India | Medical Device Registration - 0 views

arazygroup.com/blog

Safety compliance device medical consultants devices

shared by arazy-group on 20 Jul 11 - No Cached
  • arazy-group on 20 Jul 11
     
    India has strict norms and medical device regulations for drugs, medical devices, diagnostic devices and cosmetics. Arazy Group offers international standard medical device registration as the professional and reputed medical device consultants in India.
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Medical Device Market Clearance in Taiwan | Medical Device Consultants - 0 views

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Safety compliance device medical consultants devices

shared by arazy-group on 20 Jul 11 - No Cached
  • arazy-group on 20 Jul 11
     
    Arazy Group leading medical device consultants in Taiwan offering international standard in achieving market clearance and clinical review clearance for medical devices and equipment in Taiwan under the Taiwan Department of Health (DOH).
arazy-group

Medical Device Registration in Singapore | Medical Device Consultants - 0 views

arazygroup.com/blog

Safety compliance device medical consultants devices

shared by arazy-group on 20 Jul 11 - No Cached
  • arazy-group on 20 Jul 11
     
    Singapore is a promising medical device market and welcomes manufacturers with new and quality medical technology to introduce their medical products in the Singaporean market.
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Medical Device Consultants in Russia - 0 views

arazygroup.com/blog

Safety compliance device medical consultants devices

shared by arazy-group on 22 Jul 11 - No Cached
  • arazy-group on 22 Jul 11
     
    For a successful registration of medical devices in Russia, you can take help from the professional consultants of Arazy Group. 
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