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프린트
전체 257건, 현재 페이지 2/26
GPKOL
인허가
대한민국
* Improving patient access in Global & Emerging markets: Achieved optimal pricing approval between internal and external parties as Chair of the Regional Pricing Committee, with the operationalization of the Global Access and Pricing Strategy. Led the Innovative access programs in emerging markets providing strategic. Developed frontier strategies for better accessible and affordable healthcare in APAC region. Influenced internal and external stakeholders to shift price-volume to value-d access. Promoted and advocated equitable pricing methodology for better patient access (UCB Pharma). * Credible win-win partnership with stakeholders: Built a platform for the access expansion in international markets, leading the business negotiation, license in/out and governmental partnering programs (MTAC: Medical Treatment Adherence Clinics in Malaysia, CME for governmental health agencies in S. Korea, Taiwan, Thailand and Malaysia) Achieved WHO’s resolution for Psoriasis, improving patients access for optimal treatment with patient groups and WHO representatives. Advocated innovation of R&D, better patient access and ethical business practice through industry association and local government agencies with diverse partnership, programmes, and shaped external environment (LEO Pharma & MSD). * Executing Health Ecosystem Strategy: Developed the future ecosystem and payer strategy which set the global business direction and provided future vision. Oversaw the trend to shape external environment to strengthen payer engagement and partnerships with non-healthcare and leading digital transformation providers. Prepared recommendations to C-Suite and senior leadership team to promote sustainable healthcare and digital transformation within the long-term corporate strategies (UCB Pharma). • Global Patient Access • Value Strategy Formulation and Execution • Health Policy and Advocacy • Health Equity and Affordability • Partnerships: Government, Academia, Public & Media • People Leadership, Coaching and Mentoring • C-Suite and Board Engagement • Strategy and operational Excellence
중국
인허가 GMP 인허가 GMP 인허가 GMP
브라질
- Regulatory Quality Compliance. - Regulatory Affairs including product approvals and establishment of the companies (sanitary operational license and authorization). - Post-marketing surveillance (mandatory and voluntary notifications | treatement of adverse events claims) - Regulatory strategy. - Good Manufacturing Practices certification (planning, prepare, audits). - Regulatory support on import process. - Change management with uation of regulatory impact. - Risk management. - Due diligence for acquisitions.
태국
- Thailand Law and regulation on biological products (Biopharmaceuticals, Biosimilars, Vaccines, Blood products, ATMPs) - Regulatory science for pharmaceutical/biopharmaceuticals - Policy development on pharmaceuticals/biopharmaceuticals
GMP
미국
프로젝트 목표에 부합하는 다차원적 분석 데이터에 기반한 약물 설계 및 합성 생물학적 활성 물질 합성에 있어서 안정적인 물질과 방사성 물질을 사용한 종합 연구 및 실험 Method transfer와 scale up을 지원하는 분자의 화학적 프로세스 개발 및 실행 의약화학: 복합유기화합물 설계 및 합성 GMP: 제조 활동 지원 Radio Synthesis: API제조를 위한 생물학적 활성 화합물을 합성에 대한 연구 및 실험
R & D기획 인허가 기술마케팅 PM
기술마케팅 기술마케팅 기술마케팅 인허가
기술마케팅 PM
스위스
Biologics, Cell & Gene, 마이크로바이옴 (Microbiome, LBP) 분야의 스위스 및 유럽 지역 CDMO 사업개발 및 확장 관련 아래와 같은 컨설팅 업무를 수행/지원합니다. 1. Business Planning - CDMO 사업개발/확장에 필요한 Reasoning 및 전략 수립을 위한 기초 조사 및 분석 - 타겟 선정 (지역/고객/클러스터), 시장 및 경쟁사 분석 - macro/micro 환경 분석, TAM/SAM/SOM - 동향 보고: 산업동향, 기업 및 경쟁사 동향 2. 전략 수립 및 실행안 제안 - Go-to-market strategy 수립을 위한 전략툴 사용 프레임워크 수립 - 단계별 프로세스 수립 및 주요 액션아이템 도출 - Risk & Opportunity 분석 및 보완 제안 3. 실행 및 운영 - 위치 선정, 연락 사무소 혹은 법인설립, 채용 지원, 교육 (training) - 운영 관련 관리 업무(재무, 법률, 공급망/물류, Regulatory, 감사 등) 지원
기술마케팅
Legal Advise and Service in the field of Intellectual Property, Licensing, Corporate, and Marketing (미국 변리사)
Senior professional combining holistic thinking with strong problem-solving and intercultural skills gained in 15+ years working in both corporate roles and independent project assignments within the pharmaceutical industry; Broad expertise in Quality Systems and Pharmaceutical Manufacturing; Proven ability to manage multi-national and multi-disciplinary projects in an highly regulated environment; Proven track record in successfully managing Continuous Improvement and Health Authority Inspection Preparation projects; Globally recognized Coach, Mentor, Sparring Partner, and Game-Changer for Leaders, Teams, and Organizations.
