Pharmaceutical companies organize personnel to participate in drug registration regulations training-Zhejiang Jianfeng Pharmaceutical Co., Ltd.

Pharmaceutical companies organize personnel to participate in drug registration regulations training

Release time:

2021-01-26

In order to do a good job in the publicity and study of relevant policies and technical requirements, keep abreast of the latest legal developments, and strengthen communication with the national bureau, on January 15, the pharmaceutical company organized relevant personnel to participate in the online training of the latest progress report on drug registration regulations.

This training is sponsored by China Drug Administration and Research Association, and the Drug Registration Administration Department and Drug Evaluation Center of the State Drug Administration are the technical guidance units. Experts from different drug examination centers will report the reform progress of drug evaluation and approval system, newly revised supporting documents and work progress of drug registration, relevant requirements of drug post-marketing change management, and planning contents of drug technical guidelines, among them, it focuses on the detailed explanation of the trial version of the "Administrative Measures for Post-marketing Changes of Drugs" issued on January 13, and the formulation plan for the follow-up guiding principles is also explained accordingly.

At the same time, in order to facilitate colleagues from various departments to participate in the training, according to the needs of their respective workplaces, the pharmaceutical company has set up a training venue in Jinxi factory area and Qiubin factory area respectively. Colleagues from product development department, quality assurance department and pharmaceutical factory actively participated in training and online communication, raised questions according to their job requirements and received professional responses from experts. Through this training, the trainees have a deeper understanding of the latest progress of the current drug registration related laws and regulations, which has laid a good foundation for the relevant work in this position.

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