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프린트
전체 255건, 현재 페이지 15/26
GPKOL
인허가 PM
대만
Regulatory Affairs
- Regulatory Affairs : Regulatory consultation for medical devices and pharmaceutical products (excluding biosimilars) - BE study : Bioequivealence study outsourcing and inspection at Indian clinical sites - Global market PM : Project management for registration timeline for US, China, Canada, ASEAN countries
R & D기획 GMP
중국
Designing the development plan of new products based on the market demand. Colleting useful information related to the company’s R&D development.
Project Management & Regulation 1. Qualified in new Chinese medicine and natural medicine research with rich working experience - 1995–present: over 20 years in basic scientific research as well as research and development of new Chinese medicine and natural medicine, leading 3 major national new drug development projects and 27 new medicine research programs 2. Understanding of government regulations and technical requirements in Chinese medicine and natural drug research - 2001–2002: conducting pharmacology and toxicology evaluation of new Chinese medicine at the China Food and Drug Administration (CFDA) as an external expert 3. Working knowledge of technical standards of Chinese medicine and natural drug evaluation and approval I have been participating in the evaluation process as a consulting expert.
R & D기획
미국
R&D기획
R&D 기획
GMP
인허가
중국 제품 등록 가이드라인 및 인허가
임상
Medical Chart Reviewer Medical Writer