We act as a Swiss Authorized Representative (CH-REP) to the Swiss Authorities for Medical Devices Manufacturers located outside Switzerland
Freyr provides Swiss Authorized Representative (CH-REP) services to foreign medical device manufacturers for product registration and market entry in the Switzerland.
EUDAMED Production v 2.10 has been released with several new features and improvements. Are you ready for the latest and... Key Terms and Concepts in the Medical Device Regulation – Vigilance The vigilance requirements under the EU’s medical device regulations... MDCG guidance document on IVD ...
Alshedwy Group introduces its Saudi Medical Devices Authorized Representative and more regulatory services in Saudi Arabia Search Alshedwy Group EGYPT and Saudi arabia Regulatory Consulting for Medical Device and IVD Companies Need assistance complying with Saudi FDA (SFDA) medical device regulations?
EU authorized representative for medical devices, IVDD,machinery, ATEX, Pressure Equipment and Personal Protective Equipment (PPE).
a过度饮食常会导致疾病 正在翻译,请等待...[translate] aand should document the information given to the legally authorized representative and response in the patient's permanent medical record. 并且在患者的永久病历应该提供信息提供法律上授权代表和反应。[translate]...
aI,Richard H.Bell,being the Authorized Representative of Harvard Business Services, Inc.,the incorporator of RC Biotechnologies ,Inc.—a Delaware Corporation—hereby certifies pursuant to section 108 of the General Corporation Law of Delaware and to the best of my Knowledge that: I,理查H.Bell,是...
country representative, called a Malaysia Authorized Representative (AR). Your Malaysian Authorized Representative serves as your liaison with Malaysia’s Medical Device Authority (MDA) and is responsible for submitting your medical device registration, so it is important to choose your representative ...
CPC Appoints Medical Product Service GmbH As Authorized European Representative For MedClose(TM) SystemAnna Ohlden
sterilise, for the purpose of placing on the marketunder your own name, systems or procedure packs or other CE marked medical devices designed by the manufacturer to be sterilised before use; are theauthorised representativeof a manufacturer who does not have a registered place of business in ...