1. According to the company's development plan, formulate the registration strategy and plan, and promote the implementation of the project according to the plan;
2. Responsible for the compilation and application of drug registration application materials, communicate and coordinate the progress of product verification, technical review, drug testing, etc., solve various problems in the product registration process in a timely manner, and be able to communicate effectively with the authorities;
3. Responsible for registration-related issues and consultation on policies and regulations;
4. Responsible for drug clinical affairs, including communication and coordination with CRO, clinical base, PI and other clinical links;
5. Effective post-market registration maintenance for existing products;
6. Collect and study relevant industry policies and regulations, application procedures, registration regulations, etc., and grasp the latest industry trends.

*Apply email to: zhouyh@huigu.com.cn

1. Complete the analysis and testing of R&D samples;
2. Establish, optimize and verify drug quality analysis methods, complete the detection of process verification data and the confirmation of analysis methods;
3. Organize inspection records, analysis reports and other relevant test materials;
4. Complete other tasks assigned by superior leaders.

*Apply email to: zhouyh@huigu.com.cn

1. Responsible for drug prescription research and process optimization, analytical method development, formulation development and quality research;
2. Responsible for product approval materials and project application materials, and follow up on product and project approval and application progress;
3. Discuss the technical problems in the process of project implementation and propose solutions;
4. Responsible for the follow-up of drug consistency evaluation work, organization, arrangement and submission of materials.

*Apply email to: zhouyh@huigu.com.cn