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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 Device Consultants in China | Medical Device Safety compliance - 0 views

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    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 Consultants in Brazil | Medical Device Safety compliance - 0 views

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    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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    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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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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Regulatory Dossier Preparation | Medical Device Safety Compliance | Medical Device Regu... - 0 views

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    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.
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Medical Device Consultants Advice Electrical Safety Tests - 0 views

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    It is extremely important to carry out electrical safety testing for the medical device and products to ensure that the product is electrically safe. Once it is proved, the product becomes ready to be launched in the international market.
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Medical Device Registration in Russia | Medical Device Consultants Russia - 0 views

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    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 Safety compliance, Medical Device Sterilization - 0 views

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    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, Electrical Safety - 0 views

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    Arazy Group has been helping innumerable medical device manufacturers and marketers in introducing their products in the international market by carrying out medical device sterilization test for their products and equipment.
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Medical Device Consultants in India | Medical Device Registration - 0 views

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

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    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

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    For a successful registration of medical devices in Russia, you can take help from the professional consultants of Arazy Group. 
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Medical Device Registration in Argentina - 0 views

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    If you want to get your medical products registered in Argentina, you can count on the experts of Arazy Group with 15 years of experience in this domain. We provide you market clearance, clinical literature review and medical device registration in Argentina. Get in touch with us immediately to introduce and market your medical products in Argentina.
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Medical Device Consultants in Brazil - 0 views

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    Arazy Group is one of the leading medical device consultants in Brazil that offers expert regulatory services and medical device registration in Brazil for a wide variety of medical products, equipment, etc. Professional consultants of the company have more than 15 years of experience in this domain and have successfully registered thousands of medical devices in Brazil.
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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 Indonesia | medical device consultants - 0 views

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    Arazy Group are the leading medical device consultants offering medical device registration in Indonesia and gaining validation and verification for your medical devices and equipment from the important regulatory authorities in the region.
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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.
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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.
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