Group items tagged

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 around the world.

Arazy Group experts can write the clinical literature review for your product based on the existing publications and your clinical studies while complying with both the international harmonized standards and the national guidelines.

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).

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.

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.

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.

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.

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.

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.

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.

Arazy Group has been assisting medical device companies to a large extent in the launch of their products and equipment at a global level.

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 is a globally-placed and reputed medical device consultant offering expert consultation and review services to medical device manufacturers and marketers across the globe.