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프린트
전체 252건, 현재 페이지 5/26
GPKOL
인허가
중국
- 중국 인허가 절차 및 법규 - 인허가 전략 - 의약품 전략적 관리
기술마케팅 인허가 PM
터키
- Rx, OTC Procuts, Medical Device, Aesthetics & Comseitcs Marketing and Sales - In-Licensing, Out-Licensing Deals - Pharmaceutical Product Registration, Medical Device Registration
기술마케팅
- Rx, OTC Products, Medical Device, Aesthetics & Cosmetics Marketing and Sales - Effective Organization Setting & Management - Key Account Management, Lobbying, Stakeholder & Key Opinion Leader Management - Sales Training and Coaching, Sales Force Excellence
미국
- Market Access - Biotech Management & Strategy - Healthcare Policy - Patient Advocacy - Business Development & Licensing - New Business Formation
R & D기획
1. R&D Planning : All projects include R&D Planning, Clinical Trial, GMP, RA, Technical & Marketing, and PM through collaborations with Pharmaceutical companies and Medical Centers: MTTI (www.mtarget.com, PA, USA), Precision Membranes (www.precisionmembranes.com, UT, USA), BostonSight (www.bostonsight.org, MA, USA), MEEI (www.masseyeandear.org, MA, USA) and Anschutz Medical Campus (www.cuanschutz.edu, CO, USA). 2. Drug Delivery Systems (DDS) for Cancer Treatment. 3. Molecular Imaging (MI) for Cancer Detection 4. Therapeutic Contact Lens for Eye Diseases
대한민국
인도 제약바이오시장 진출 관련 컨설팅
기술마케팅 PM
멕시코
- Technical & Marketing: To provide training and consulting on overseas expansion strategy and marketing channel development in such case of Korean companies’ market expansion into emerging countries like LATAM - Project Management: To provide training and consulting on the full cycle of new drug development and commercialization by cross functional leadership from R&D planning, clinical trial and production (GMP) to regulatory affairs (RA) and technical marketing (BD)
인허가 GMP
- CMC: Technical/regulatory advices on gene therapy, biosimilar or biotechnology products development (i.e., manufacturing process, QC specifications, comparability, CRO/CMO, etc.) - RA: Regulatory strategies and interaction with US FDA for preclinical , clinical, BLA, and postmarketing preparation - GMP: regulatory guidance and manufacturing facility inspections
임상
1. Clinical Development Plan : Develop TPP and CDP according to company strategy and produce profile as well the therapeutic area guidelines. 2. Clinical Trial : Project management on full function study team, Outsourcing Management, Clinical Operation team management, China GCP. 3. China Regulatory Policy : China IND to NDA, Global Development Strategy for China market
R & D기획 임상 인허가
1. R&D Planning for oncology drug 2. Clinical Trial design and implementation in oncology area 3. Regulartory Affairs(RA)