Regulation Training and Interpretation
- Categories:Strategy Consultation
- Time of issue:2021-06-09 16:01:39
With a reliable service attitude, we have been committed to professional training in the industry. We hope that through training, we will send outstanding talents to the filing and registration market of pharmaceuticals, medical devices, IVD and cosmetics, which will benefit the enterprise and contribute to the society. If your company has related needs, we look forward to your company getting in touch with us.
➣ Service Scope:
1.Training and interpretation of relevant medical device regulations;
2.Training of medical device operation quality management standards;
3.GCP/GMP standard training;
4.Project-related professional basic knowledge;
5.Subject management of clinical trials;
6.Clinical data management;
7.Clinical data quality control;
8.Clinical trial skills;
9.Clinical trial management training;
10.Training on job responsibilities of clinical coordinators;
11.Clinical coordinator communication skills.
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The company specializes in medical device registration, in vitro diagnostic reagents registration, cosmetics agent service company, committed to the NMPA, CE regulation research and product registration and certification service has been more than 17 years.