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 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).
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.
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.
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.
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, 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, 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.
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.
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.
http://www.arazygroup.com - Ministry of Health clearance or MOH clearance throughout the Middle East, Africa and Asia for medical device registration and regulatory services.
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 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.
Arazy Group offer quality and vital medical device consultation for ensuring market clearance and meeting quality standards in the medical device industry in Turkey.
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.
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.
Arazy Group offer complete third party lab services for medical device packaging and sterilization validation for any device and any risk classification.
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.
Arazy Group offers a wide range of medical device consultations for fulfilling the different norms and specifications mandatory for medical device clearance and market entry all over the world.
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.
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.
Arazy Group offers a wide range of medical device consultations for fulfilling the different norms and specifications mandatory for medical device clearance and market entry all over the world.
http://www.www.arazygroup.com/US-FDA-Agent - Medical device validation, FDA certification, CE Mark clearance, and regional medical device registration and global authorized representatives.