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Regulatory
Affairs

Shenzhen Beimei Pharmaceutical Co., Ltd. has a professional registration team. Team members have rich experience in registration affairs, pharmaceutical research, and clinical affairs. We can quickly implement domestic registration declaration of imported and R&D products in accordance with the requirement of domestic registration regulations. In the perspective of new product approval, through systematic data research and professional evaluation, a project registration strategy report is formed to provide strong support for product development and business negotiations. In the registration phase of imported products, RA team cooperates closely both with the company's BD team and partners. From data pre-review, technical exchange, data translation, filing data collation, registration communication and etc., we have formed an efficient operation mode. In the registration of R&D products, RA team focuses on working closely with the company's R&D team. In this phase, it is involved in the product development process to ensure that prescription development and quality research meet the requirements of various registration regulations.

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