home > 전문가 컨설팅> 온라인 컨설팅서비스> 컨설팅 신청
프린트
전체 260건, 현재 페이지 11/26
GPKOL
인허가
스페인
- EU Regulatory Strategy, European registration through the Centralized and the Mutual Recognition/Decentralized procedures - EMA: Orphan Drug Designations, Scientific Advice, Briefing Meetings - European Member States: scientific advices and other consultations
인허가 GMP
브라질
- Regulatory affairs: Register of products in ANVISA, including the obtaining of necessary license and certificates - GMP: Prepare the company for Sanitary Inspection to obtain the Brazilian GMP (CBPF), and other required certificates
기술마케팅
대한민국
- INN/USAN(Global Regulation/Requirement): Availability Check, Development, Review, Submission, Consultation(유럽 및 미국 시장 진출 관련 성분명 허가 심사 자문) - Global Clinical Name&Logo(Pre-Marketing): Development Consultation(신약의 Global L/O, 환자모집, Publication 전략) - Global Brand Name&Logo: FDA, EMA, Health Canada, MHLW(Japan) brand name development and document preparation/consultation
인허가 임상 R & D기획
러시아
- Regulatory affairs: Appropriate rules governing medicinal products for human use in Russia, EAEU, and EU - Clinical Trial: Scientific aspects of clinical development, medical writing - R&D 기획: Development of generic and biosimilar medicinal products; new chemical entities/biologics
사우디아라비아
- Registriation in KSA(GCC)
임상 인허가
미국
- Regulatory affairs/clinical research professional with extensive experience in regulatory affairs, clinical research and drug development at FDA, NIH, and industry, emphasizing drugs, biotechnology and medical device products. - Experience in the use of computers in document preparation and submission, IND/NDA submissions, adverse experience reporting, clinical regulatory compliance and strategic planning
임상
- GCP Managment/START-up(Country&Site approach&selection)/Trial Operation Management - Global Project Start-up & Management/Technology & Process/Business Development - Quality Managment for Clinical part/Auditing & CAPA strategy - Resource & talent training in bio-industry (Productivity & efficiency management) - EP unit set up & business
과테말라
- 과테말라 의약품 무역 등 중미 진출 관련 자문
GMP
- 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