International Registration

Quarkmed has professional knowledge and abundant experience in drug registration and is familiar with the regulations of various countries, and is capable of providing comprehensive registration consultation and support services. The scope covers China, the United States, Europe, Australia and other places, which will help enterprises reduce drug registration risks, improve registration efficiency, shorten the registration cycle, and provide comprehensive and high-quality drug international registration services for pharmaceutical companies.

Content of the service

• Feasibility assessment

• Development of drug registration strategy: Development of drug registration strategy by taking global adaptability, clinical trial schedule, declaration process, regulations and other factors into account.

• Clinical trial design and implementation: Provide organizations and institutions of clinical trial support and services to help enterprises and research institutions complete clinical trials smoothly and efficiently, and provide quality assurance and compliance assurance

• Application of drug registration : Provide pharmaceutical companies with the whole process of drug/drug and device registration application support

• Regulatory communication and coordination: Establish contacts with national drug regulatory agencies, coordinate multi-party resources, and complete the approval and application process of registration affairs.