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MITRO provides all-around radiopharmaceuticals regulatory consulting, professional technical services and compliance suggestions for domestic and oversea pharmaceutical companies. MITRO also sets up the internationally standardized quality control system and a series of standard operating procedures (SOPs) to ensure the quality of services and the compliance with relevant regulations of China FDA. In addition, MITRO has significant competitive advantages in radiopharmaceuticals registration: With good cooperation relationship with CDE experts and clinical trial CROs, MITRO can largely expedite the service processes.

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