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Global Medical Device Service | GMDN | European Authorized Representative | Medical Dev... - 0 views

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    Global Medical Device Nomenclature is a system of internationally harmonized generic descriptors used to identify all medical products. Such products include those used in the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
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    GMDN or Global Medical Device Nomenclature is a system of internationally harmonized generic descriptors used to identify all medical products. Such products include those used in the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
arazy-group

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.
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 Oman | Medical Device Consultants Oman - 0 views

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    Depend on the international standard medical device consulting services of Arazy Group, global leaders in medical device registration and clinical clearance. We offer quality and proven medical device registration in Oman to medical device manufacturers and marketers eyeing the region to introduce their new set of medical products.
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    Depend on the international standard medical device consulting services of Arazy Group, global leaders in medical device registration and clinical clearance. We offer quality and proven medical device registration in Oman to medical device manufacturers and marketers eyeing the region to introduce their new set of medical products.
arazy-group

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

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    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.
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    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 Registration Kuwait | Medical Device Consultants Kuwait - 0 views

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    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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    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

Medical Device Registration | Global Medical Device Registration | Medical Devices Stan... - 0 views

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    As an international company, we make sure we are available to our clients around the clock through various channels of communication in multiple languages.
arazy-group

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 Software Validation | Medical Device Software Validation | Medical Device Desig... - 0 views

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    Arazy Group has been assisting medical device companies to a large extent in the launch of their products and equipment at a global level.
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    Arazy Group is one of the leading global names in medical software Validation offering a wide range of medical device regulatory services, medical device software and clinical literature review for medical device manufacturers and distributor around the world.
arazy-group

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

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    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.
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    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 Devices Experts, Quality Medical Devices - 0 views

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    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

Medical Device Approval Japan | Medical Device Regulatory Vietnam - 0 views

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    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.
arazy-group

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

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    Medical Device specific regulation strategy reports, Medical Device Registration with COFEPRIS, COFEPRIS Technical documents Preparation, Mexico license holder and local Authorize Representative and Arazy Group's unique line of GlobaR - Global Regulatory Hub™ products.
arazy-group

Medical Devices in Australia | Medical Device Consultants - 0 views

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    Medical Device Specific regulation strategy reports in Australia, Medical Device Registration with the TGA, Australia Sponsor Representation for Medical Device manufacturers and TGA Technical documents Preparation and Arazy Group unique line of GlobaR - Global Regulatory Hub™ products.
arazy-group

Medical Device Registration in South Africa | Medical Device Consultants - 0 views

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    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.
arazy-group

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

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    Arazy Group is a leading global medical device regulatory and consulting firm offering localized and standard quality services in Columbia as well.
arazy-group

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.
arazy-group

FDA US Agents | FDA Registration US | FDA Regulatory | Compliance FDA 510 | FDA US Agen... - 0 views

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    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).
arazy-group

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

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    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

Medical Device Software | Medical Device | FDA | Medical Software Validation | Medical ... - 0 views

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    Arazy Group is a leading global name in medical software Validation offering a wide range of medical device regulatory services, medical device software and clinical literature review for medical device manufacturers and distributor around the world.
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