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전체 253건, 현재 페이지 11/26
GPKOL
기술마케팅
과테말라
- 과테말라 의약품 무역 등 중미 진출 관련 자문
GMP
미국
- API CMC: API CMC (Active Pharmaceutical Ingredient: chemistry, manufacturing , and controls), including route selection, process optimization, scale-up, tech transfer for cGMP manufacturing - Solid polymorphism: Crystallization, polymorph screening and the control - Oligonucleotide: Detailed process chemistry support for raw material management of cGMP oligonucleotide manufacture, including supplier qualification, supplier audit, and developing raw material control strategy such as setting and justifying specifications.
임상 인허가 R & D기획
- Clinical trials, - R&D Planning, - Regulatory Affairs
R & D기획
- Antibody: Antibody discovery, Andtibody drug development - Cell line development: Cell line development for antibody production - Antibody optimization: Affinity maturation for lead optimization
- R&D Planning and strategy: All area of Early Discovery R&D planning and strategy including and not limited to hit discovery, hit to lead, Target ID, Target Validation - Company founding & management - Key Technology / Scientific discovery
대한민국
- 국내기술 해외이전/Partnering - 국외기술 국내이전 - 시장요구 반영을 통한 NCE 개발, Drug Discovery 지원, Target area 선정 - 기술개발 로드맵 작성 지원
- Drug Discovery(R&D): Structure-based drug design in cancer, neurodegenerative diseases (Parkinson’s Disease), malaria and dengue
인허가
브라질
- GMP: Quality System management and Good Drug Manufacturing Practices. - RA: Preparation and submission of generic and biological drug registration dossiers with ANVISA.
- Innovation: Manager of Business Incubator, Technological Park, Venture Capital Fund, Research Labs and Institute of Innovation, R&D Planing and execution for drug development, and Management of Research Groups. - Life Science: Manager of the Technological Park of Life Sciences, Project Leader of Drug Development, PDP program developer and Manager, Designer of partnership architecture to technology transfer for drug development, Designer of International Program Alliances(South Korea, France, US, Europe) - Regulatory: Developer of Strategic Planning for ANVISA, Designer of Prganizational structure for ANVISA, Designer of the Knowledge Regulatory Affairs Reference Center, Good Laboratories & Manufacturing Practices Registration, Pre-Clinical and Clinical Trials Planning.
임상
- Clinical Trial: Monitoring of clinical trial related to Regular Heparin - Science Publishing: Member of Publishing Service of Wolters Kluwer Pharma Solutions - Business Development: Several Projects to become in products following steps in RA, GMP inspections Marketing, R&D