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Major Challenges of Medical Device Industry - 0 views

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    Every industry has been facing several challenges to deliver best of products and services. Medical device industries have always faced challenges related to technology, reimbursement and market risk, regulatory and the latest financing risk.
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Medical Device Registration South Africa| Medical Device Services | Medical Devices |Me... - 0 views

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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in South Africa. You can introduce your medical device, IVD or medical device equipment into the South African medical device industry with our expert help and assistance.
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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in South Africa. You can introduce your medical device, IVD or medical device equipment into the South African medical device industry with our expert help and assistance.
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Medical Device Registration in Israel| Medical Device Services | Medical Devices | Medi... - 0 views

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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in North America. You can introduce your medical device, IVD or medical device equipment into the North America device industry with our expert help and assistance.
arazy-group

Medical Device Registration in Norway| Medical Device Services | Medical Devices | Medi... - 0 views

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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in Norway. You can introduce your medical device, IVD or medical device equipment into the Norway medical device industry with our expert help and assistance.
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Medical Device Design Africa| Medical Device Registration Africa| Medical Device Servic... - 0 views

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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in South Africa. You can introduce your medical device, IVD or medical device equipment into the South African medical device industry with our expert help and assistance.
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Medical Device Registration Australia | Medical Device Services | Medical Devices | Med... - 0 views

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    Arazy Group helps you understand the required EU directives in relation to the medical device industry in Australia. You can introduce your medical device, IVD or medical device equipment into the Australian medical device industry with our expert help and assistance.
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Medical Device Industry| Expertise Regulatory Service| Medical Technology | Medical Dev... - 0 views

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    We invite you to join Arazy Group Medical Device Consultants to share your knowledge with us and get paid (well) for your contribution.
arazy-group

Expertise Regulatory Service| Medical Technology | Medical Device Industry| Medical Dev... - 0 views

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    Medical device consultants are equipped with proficient tradesmen who would have the complete understanding in what it takes to introduce a new medical device in the market and that too, in a most competent, time effective and rationalized manner.
arazy-group

Universal Authorized Representative | USA Designated Agent | Global Regulatory Represen... - 0 views

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    Arazy Group Universal Authorized Representativeā„¢ 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 Representativeā„¢ service takes away this burden and eliminates the need for multi legal contracts and different foreign currencies. AG Universal Authorized representativeā„¢ services is your single source for a global regulatory representation.
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Medical Device Consultants in Malaysia | Medical Device Registration - 0 views

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    Arazy Group offering a wide range of clinical literature review and regulatory authorities to comply with the important regulatory norms and specifications in the Malaysian medical device industry.
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Medical Device Registration In Turkey | Medical Device Consultants Turkey - 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 Turkey. medical device registration in turkey, medical device consultants turkey, medical device.
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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.
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Medical Device Consultants in Argentina | Medical Device Registration - 0 views

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    Arazy Group is a leading name in regulatory affairs and quality assurance in the medical device industry in Argentina.
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Medical Device Consultants in Turkey | Medical Device Registration - 0 views

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    Arazy Group offer quality and vital medical device consultation for ensuring market clearance and meeting quality standards in the medical device industry in Turkey.
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Italian NSIS Repertorio Registration | Medical Devices | CE Marked | National Regulatio... - 0 views

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    Medical devices of all classes, active implantable devices and procedure packs and kits sold in Italy to the Public Sector must be registered in an Italian database ("Repertorio"), administered by the Ministry of Health through its new system, NSIS.
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    Medical devices of all classes, active implantable devices and procedure packs and kits sold in Italy to the Public Sector must be registered in an Italian database ("Repertorio"), administered by the Ministry of Health through its new system, NSIS.
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US FDA Agent | Medical Device Registration | Medical Devices | CE Marked | National Reg... - 0 views

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    Arazy Group US company is Medes USA Inc., located in Seattle, Washington. Medes USA is a qualified and a recognized Regulatory Designated Agent.
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    Arazy Group US company is Medes USA Inc., located in Seattle, Washington. Medes USA is a qualified and a recognized Regulatory Designated Agent. We have been serving hundreds of companies worldwide since the new FDA regulation came into force on April 2002.
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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.
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Medical Device Services South Africa| Medical Devices |Medical Device Registration Sout... - 0 views

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    Arazy Group, a Universal medical device consultant, offers medical device verification, validation as well as certification services in South Africa.
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Clinical Research Administration, High Quality Clinical Research | ISO 1348 | 510K Appr... - 0 views

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    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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