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EU Health Authority | Medical Device Authority | Medical Device Service |EU Certificate... - 0 views

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    For medical devices cleared for sale with the USA - FDA, a Certificate for Foreign Governments (CFG) can be issued instead of a CFS. Select the "type of service required "available in the attached form for more information of CFG.
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Universal Authorized Representative | USA Designated Agent | Global Regulatory Represen... - 0 views

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    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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    Arazy Group Medical Devices Consultant is a reputed medical device consultant for medical device registration in Japan and deals with quality medical devices. In fact it is a global medical device consultant offering registration of medical device services in more than 53 countries.
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    Arazy Group is a leader in medical device consultancy and medical device registration services throughout the world. Professional medical device consultants are available to help the companies to avoid problems or risks related to regulation.
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    Medical device industry is counted among industries that play effective role in the society. They come up with quality medical devices which are quality tested and authorized by medical researchers and regulatory specialists to ensure the safety and effectiveness of devices.
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    Arazy Group Universal Authorized Representative™ service takes away this burden and eliminates the need for multi legal contracts and different foreign currencies. AG Universal Authorized representative™ services is your single source for a global regulatory representation.
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EU Certificate of Free Sales (CFS) | Medical Device Consultants - 0 views

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

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    Arazy Group offer complete third party lab services for medical device packaging and sterilization validation for any device and any risk classification.
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    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.
arazy-group

Essential Requirements | Medical Device | FDA |Regulatory Designated Agent | FDA Device... - 0 views

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    Arazy Group - Preparation of a regulatory dossier for the authorities can be cumbersome as It may contain tens of different documents, templates, reports, charts and graphics.
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    Arazy Group helps 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.
arazy-group

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

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    MDR procedure describing a system for the notification and evaluation of adverse incidents to be known as the Medical Devices Vigilance System.
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    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 Clearance for Global Launch of Products - 0 views

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    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. 
arazy-group

Medical Device Consultants - 21CFR 820, FDA QSR, cGMP - 0 views

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    for any assistance you may need for the preparation or implementation of GMPs. We also provide step by step guidance, external auditing, online consulting and fully outsourced quality assurance maintenance services for your organization.
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Canadian Medical Devices Conformity | CMDCAS Canadian Medical Device Conformity - 0 views

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    To register of a medical device in the Canadian market a quality management systems must be applied for all medical devices manufacturer except class for I devices. Canadian Medical Devices Conformity, CMDCAS Canadian Medical Device Conformity, Canada.
arazy-group

Medical Device Approval Palestinian China | Medical Device Regulatory China - 0 views

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    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 Brazil | Brazil Medical Device Consulting - 0 views

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    Find qualified consultants for the Brazil medical device industry at arazygroup.com Medical Device specific regulation strategy reports, Medical Device Registration with ANVISA, Brazilian Representative and certification holder for Medical Device man.
arazy-group

Medical device registration Bahrain | Medical Device Consultants Bahrain - 0 views

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    Gain medical device market clearance in Bahrain with expert medical device registration services of Arazy Group. Leaders in global medical device consultancy, we offer international standard verification and validation services for your medical products in the Bahrain market.
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    Gain medical device market clearance in Bahrain with expert medical device registration services of Arazy Group. Leaders in global medical device consultancy, we offer international standard verification and validation services for your medical products in the Bahrain market.
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Medical device registration Jordan | Medical Device Consultants Jordan - 0 views

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    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.
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    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.
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Medical Device Consultants | Risk Management Report - 0 views

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    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.
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Clinical Development Planning | Trial Design Planning | Medical Device Listing | Clinic... - 0 views

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    Arazy Group team of experienced clinical and regulatory professionals can assist you in developing a comprehensive clinical development strategy for your device at every stage of product development.
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    Arazy Group is a leading global name in medical device consultancy offering a wide range of medical device regulatory services and clinical literature review for medical device manufacturers and distributors in the region.
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FDA 510 | FDA US Agents | FDA Device Listing | FDA US Agents | FDA Registration US | FD... - 0 views

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    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.
arazy-group

21CFR 820 | FDA QSR | cGMP -FDA GMP Audits to QSR 21 CFR Part 820 for Medical Device C... - 0 views

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    GMPs are guidelines that outline the aspects of production and testing that can impact the quality of a product. Many countries have enacted that pharmaceutical and medical device companies must follow GMP procedures and have their own criteria that correspond with their legislations.
arazy-group

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

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    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 Consultants | Medical Devices Experts | Medical Lab Equipment - 0 views

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    Arazy Group expertise is regulatory affairs and quality assurance for the medical device industry. We specialize in marketing safe and effective Medical Technology to international markets. Our experienced consultants are responsible for the successful registration of thousands of medical devices globally. Our customized solutions accommodate all stages of medical device's life cycle and our adaptable services fit any application and any size organization.
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Arazy Group | Medes | MDC | Medical device consultants in USA - 0 views

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    http://www.arazygroup.com/medical_device_registration_in_usa_ - Medical device consultants in USA for FDA clearance services and fulfilling FDA requirements for medical devices, IVDs etc.
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