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US FDA Clearance | Medical Device Safety compliance - 0 views

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shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    us fda clearance us fda approval, fda approval, fda regulations, fda approval process, fda standards, fda clearance vs approval, us fda certification.
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Technical File Preparation | CE Mark Certification | Medical Device Regulation | CE Mar... - 0 views

www.arazygroup.com/TechnicalFilePreparation

technical file preparation CE mark certification medical device regulation consultants FDA approval process directive submission regulatory registration 93_42 EEC ISO 1448

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Arazy Group is a leading medical device consultant that provides medical device manufacturers with international acceptance, right product validation, medical device registration, product regulatory and marketing approvals to help them gain market approval for their medical devices and equipment.
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Clinical Evaluation through Literature Review | Clinical Literature Review |Medical Dev... - 0 views

www.arazygroup.com/ClnLiterRev

clinical evaluation through literature review medical device regulatory CE marking consultants approval

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Gain CE Mark approval and fulfill the CE mark requirements with the help of our global experts and team of qualified marketing professionals, regulatory specialists, scientists and the best brains behind achieving product validation for medical device manufacturers and distributors around the world.
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Clinical Research Administration, High Quality Clinical Research | ISO 1348 | 510K Appr... - 0 views

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shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    The Clinical Research Administrator facilitates the timely execution and completion of high-quality clinical research by assisting investigators and industry sponsors with all aspects of the clinical research.
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Medical Device Registration in Russia | Medical Device Approval Russia - 0 views

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Medical Device Registration Consultants Approval Expert

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Arazygroup.com - Medical Device specific regulation strategy reports, Medical Device Registration with Roszdravnadzor, Technical documents Preparation, obtaining GOST-R quality and safety certification, obtaining sanitary and epidemiological conclusi.
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Medical device registration Lebanon | Medical Device Consultants Lebanon - 0 views

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Medical registration Lebanon Devices Device Consultants

shared by arazy-group on 25 Jul 11 - No Cached
  • arazy-group on 25 Jul 11
     
    Arazy Group, the global medical device consulting firm offers medical device registration in Lebanon to domestic as well as overseas medical device and equipment manufacturers. You can foray into the Lebanese market with your medical products after gaining market approval and clearance from the different medical and health regulatory bodies in Lebanon.
  • arazy-group on 26 Jul 11
     
    Arazy Group, the global medical device consulting firm offers medical device registration in Lebanon to domestic as well as overseas medical device and equipment manufacturers. You can foray into the Lebanese market with your medical products after gaining market approval and clearance from the different medical and health regulatory bodies in Lebanon.
arazy-group

Medical Device Approval | Universal Authorized Representative - 0 views

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Medical Device Registration Consultants Approval Regulatory

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    Arazy Group Universal Authorized Representative™ service takes away this burden and eliminates the need for multi legal contracts and different foreign currencies.
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Sterilization Validation of Medical Devices | Medical Device Safety Compliance | Medica... - 0 views

www.arazygroup.com/Sterilizofedicalevices

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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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Clinical Study Management, Clinical Development Planning |Medical Device Regulatory| Me... - 0 views

www.arazygroup.com/StudyManagement

clinical study management development planning medical device regulatory CE marking consultants approval

shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Clinical trials planning and design are based on the therapeutic principles, regulatory standards and guidance documents, background literature and labeling of equivalent products.
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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 Approval Palestinian China | Medical Device Regulatory China - 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
     
    Arazy Group deals in regulatory affairs and quality assurance for the medical device industry. It offers offer registration of medical device services in China. Medical Device specific regulation strategy reports, for more information, please submit..
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Medical Device Registration in South Africa | Medical Device Consultants - 0 views

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Medical Device Registration Consultants Approval Regulatory

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 South African MOH, local Representative and certification holder for Medical Device manufacturers, MCC Technical documents preparation and Arazy Group's unique line of GlobaR - Global Regulatory Hub™ products.
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Medical Device Consultants Korea | Medical Device Regulatory Korea - 0 views

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Medical Device Registration Consultants Approval Regulatory

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 KFDA, KFDA Technical documents Preparation, license holder and local Authorize Representative.
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Clinical Evaluation through Literature Review - Medical Device Consultants - 0 views

www.arazygroup.com/LiteratureReview

Medical Device Registration Consultants Approval Regulatory

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    Arazy Group experts can write the clinical literature review for your product based on the existing publications and your clinical studies while complying with both the international harmonized standards and the national guidelines.
arazy-group

EU Certificate of Free Sales (CFS) | Medical Device Consultants - 0 views

www.arazygroup.com/SaleCertificates

Medical Device Registration Consultants Approval Regulatory

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    For medical devices cleared for sale with the USA - FDA, a Certificate for Foreign Governments (CFG) can be issued instead of a CFS.
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Medical Device Consultants | Risk Management Report - 0 views

www.arazygroup.com/RiskAnalysis

Risk Analysis Management Report Medical Device Registration Consultants Approval Regulatory

shared by arazy-group on 29 Jul 11 - No Cached
  • arazy-group on 29 Jul 11
     
    Medical Device Risk Management and Risk Analysis, Medical Device Risk Analysis, Risk Management for Medical Devices, For more information, please submit your inquiry or choose to consult our online experts right now.
arazy-group

Product Registration Spanish Database | Medical Device Registration | Clinical Trial Mo... - 0 views

www.arazygroup.com/tRegistrationinSpanishDatabase

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shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Gain CE Mark approval and fulfill the CE mark requirements with the help of our global experts and team of qualified marketing professionals, regulatory specialists, scientists and the best brains behind achieving product validation for medical device manufacturers and distributors in Europe.
arazy-group

FDA Consulting | FDA Consulting Privacy Policy | Medical Device Consultant| EMC Certifi... - 0 views

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shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Medical device companies have faced regulatory, technological, reimbursement and market risks always. It can be said that these risks are not new, a new risk is added to the present set of challenges and that risk is called as financing risk.
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Usability Studies | FDA | Medical Device Design | FDA Medical Device | Medical Device R... - 0 views

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shared by arazy-group on 22 Sep 11 - No Cached
  • arazy-group on 22 Sep 11
     
    Leaders in global medical device consultancy, Arazy Group offers international standard verification and validation services for your medical products in market.
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FDA Clearance for Global Launch of Products - 0 views

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FDA Clearance Medical Device approval

shared by arazy-group on 08 Sep 11 - No Cached
  • arazy-group on 08 Sep 11
     
    A large number of medical developers and manufacturers are there who are seeking help from Arazy Group in getting FDA Clearance for international acceptance of their products. 
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