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IVD | GMP Certificates| Medical Device Manufactures | Vitro Diagnostics Products | Audi... - 0 views

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    Foreign and local medical device manufacturers are now required to be inspected and be in compliance with the Brazilian Good Manufacturing Practices requirements prior to the submission of their devices for registration with ANVISA, the Brazilian authority in charge of the medical devices and IVDs clearance.
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SOP | Clean Room procedures | Medical Devices| Manufacture of Medical Devices | Special... - 0 views

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    Arazy Group Bank of SOPs includes procedures for most of the manufacturing processes practiced in the MedTech industry under various environmental conditions.
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Annual Registration Renewal | Product Registration| Professional Consultation | Manufac... - 0 views

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    Arazy Group provide online and/or onsite assistance in preparation of any third party audits and our consultant can escort you at the time of the audit.
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    Registration renewal is very important to maintain your product sales clearance and registration for as many years as possible. Renewal of product registration is mandatory in many markets and is subjected to a variety of requirements dictated by local authorities.
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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.
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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.
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Regulatory Authority | Medical Device Services | Universal Authorized Representative Se... - 0 views

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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 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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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 Registration in Thailand | Medical Device Consultants Thailand - 0 views

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    Medical Device specific regulation strategy reports, Medical Device Registration with Thai FDA, Thai Representative and certification holder for Medical Device manufacturers, Thai FDA Technical documents preparation and Arazy Group's.
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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.
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Medical Device Regulations for Argentina | Argentina Registration Expert - 0 views

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    Arazygroup.com - Services in Argentina include in Argentina medical devices are regulated by The National Administration of Drugs, Food and Medical Technology (ANMAT) under the Ministry of Health. Medical products whether they are manufactured or imp.
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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.
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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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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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Technical File Preparation | CE Mark Certification | Medical Device Regulation | CE Mar... - 0 views

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    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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Universal Authorized Representative | FDA Regulatory | Compliance FDA 510 | FDA US Agen... - 0 views

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    European Union (EU) Authorized Representative, USA Designated agent, China after Sales service, Central & South American registrations holding companies, Japan MAH - Marketing Authorized Holder, Product Sponsor and similar entities are the legal and regulatory bodies a medical device manufacturer needs to source, appoint, contract, pay for and renew annually in order to fully satisfy the product sales clearance requirements.
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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.
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EU Certificate | EU Certificate of Free Sales| CFS | FDA | EU Health Authority | Medica... - 0 views

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    Most foreign health authorities require a manufacturer to present a Certificate of Free Sales (CFS) from the country of origin or the European Union (EU) as part of the requirement for the medical devices import certificate in their territories.
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