Loading…
This event has ended. Visit the official site or create your own event on Sched.
Emerging Markets [clear filter]
Wednesday, June 29
 

2:00pm EDT

#343: Strategies, Enablers, and Barriers to Medicine Development in the Emerging Markets: The 2025 Global Regulatory Landscape
Limited Capacity seats available

Component Type: Session
Level: Intermediate
CE: ACPE 1.25 Knowledge UAN: 0286-0000-16-546-L04-P; CME 1.25; IACET 1.25; RN 1.25

Companies’ global development strategies and the competency of many maturing regulatory authorities are evolving. Which practices and processes will lead to an optimal future regulatory environment that expedite availability of new medicines?

Learning Objectives

Identify current global development and submission strategies for new medicines; Describe potential changes to the global regulatory landscape over the next ten years and realistic scenarios for regulatory review as medicines regulation evolves based on regulatory science; Discuss current and future regulatory barriers to global development and licensing and possible potential solutions.

Chair

Prisha Patel, MSc

Speaker

Industry Perspective
Joseph C. Scheeren, PharmD

WHO Perspective on Medicines Development in the Emerging Markets
Mike Ward



Chair
PP

Prisha Patel

Manager, Global Development Programme, Centre For Innovation In Regulatory Science (CIRS)
Prisha Patel is the Manager for the Global Development programme at the Centre for Innovation in Regulatory Science (CIRS), London, focusing on emerging markets. Her responsibilities include managing the emerging markets industry benchmarking and agency benchmarking projects and working... Read More →

Speakers
avatar for Joseph Scheeren

Joseph Scheeren

Senior Vice President, Head Regulatory Affairs, Pharma and Consumer Health, Bayer
Joseph Scheeren, Pharm.D. is Senior Vice President, Global Head of Regulatory Affairs Pharma & Consumer Health at Bayer. He has 30+ yrs exp. as Global Regulatory Affairs professional (France, Germany, Switzerland, US & China). He is an active member of the DIA Board of Directors... Read More →
avatar for Mike Ward

Mike Ward

Coordinator, Regulatory Systems Strengthening, EMP, World Health Organization (WHO)
Mike Ward is Coordinator of the Regulatory System Strengthening Team, Department of Essential Medicines and Health Technologies, Health Systems and Innovation Cluster, WHO Headquarters; he joined WHO as the Coordinator, Prequalification Team, in this same Department. He previously... Read More →


Wednesday June 29, 2016 2:00pm - 3:15pm EDT
201B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA
  Trk 08: Reg Affairs, Session
 

Filter sessions
Apply filters to sessions.
  • Preconference Tutorial
  • Trk 01: Clinical Operations
  • Trk 02: Proj-Port Mgt-Strat Planning
  • Trk 02: Proj/Port Mgt/Strat Planning
  • Trk 03: Innov Part Model-Outsourcing
  • Trk 03: Innov Part Model/Outsourcing
  • Trk 04: Preclin Transl-Early Clin Dev
  • Trk 05: Reg of Prod Adv-Mkting
  • Trk 05: Reg of Prod Adv/Mkting
  • Trk 06: Med Comm-Wrtg-MSL
  • Trk 06: Med Comm/Wrtg/MSL
  • Trk 07: Tech-Data- Records-Subs
  • Trk 07: Tech/Data/ Records/Subs
  • Trk 08: Reg Affairs
  • Trk 09: Med Devices-InVitro-CombProd
  • Trk 09: Med Devices/InVitro/CombProd
  • Trk 10: Pub Pol-HealthCare Compl-Law
  • Trk 10: Pub Pol/HealthCare Compl/Law
  • Trk 11: Quality in CT-GCP
  • Trk 11: Quality in CT/GCP
  • Trk 12: Pharm Quality
  • Trk 13: CER-Glob Health Econ
  • Trk 13: CER/Glob Health Econ
  • Trk 14: Clin Safety-PV
  • Trk 14: Clin Safety/PV
  • Trk 15: Statistics
  • Trk 16: Prof Development
  • Trk 17: Rare-Orphan Diseases
  • Trk 17: Rare/Orphan Diseases
  • Trk 18: Global Regulatory
  • Trk 19: DIAmond
  • Trk 20: Innov Theater
  • Trk 21: Poster Presentations
  • Trk 22: Engage and Exchange
  • Trk 23: Opening Plenary
  • Credit Type
  • ACPE
  • CME
  • IACET
  • PMI
  • RN
  • Audience
  • Advanced
  • Basic
  • Intermediate
  • Featured Topics
  • 21st Century Cures
  • Agency Participation
  • Approval Pathways
  • Audits and Inspections
  • Benefit-Risk
  • Big Data
  • Biologics-Biosimilars
  • Clinical Trial Designs
  • Clinical Trial Transparency-Clinical Trial Disclos
  • Cloud Computing
  • Community-led-Scientific Working Group Offerings
  • Current Issues in Policy and Law
  • Design Thinking
  • Disease Specific
  • Disruptive Technologies
  • Electronic Health Records (EHR)
  • Emerging Markets
  • GDUFA-Generics
  • Hot Topics in Policy and Law
  • IDMP
  • Increasing Research and Development Innovation
  • Interactive Workshop
  • Labeling
  • Mobile-Wearable Technology
  • Observational Studies
  • Partnership Strategies
  • Patient Engagement
  • Patient Recruitment and Retention
  • Patient Registries
  • Pediatrics
  • Precision-Personalized Medicine-Targeted Therapy
  • Pricing- Reimbursement and Access
  • Program Offerings for Student Attendees
  • R&D Innovation
  • Regulatory Harmonization-Convergence
  • Risk Evaluation and Mitigation Strategies (REMS)
  • Risk-Based Monitoring
  • Social Media Strategies
  • Topics Related to Asia-Pacific Region
  • Topics Related to Canada
  • Topics Related to China
  • Topics Related to Europe-EMEA
  • Topics Related to India
  • Topics Related to Japan
  • Vaccines
  • Value-Based Evidence
  • Women's Health
  • Interest Area
  • Academic Health Centers-Investigative Sites
  • Advertising & Promotion
  • Biotechnology
  • Clinical Data Management
  • Clinical Data Management - eClinical
  • Clinical Research
  • Clinical Safety & Pharmacovigilance
  • Clinical Supplies
  • CMC
  • CMC-GMP
  • Combination Products
  • Comparative Effectiveness
  • Document & Records Management
  • eClinical
  • Finance
  • Good Clinical Practices & QA
  • Information Technology
  • Manufacturing
  • Marketing & Sales
  • Medical Communications
  • Medical Devices & Diagnostics
  • Medical Science Liaison
  • Medical Writing
  • Non-clinical Safety
  • Outsourcing
  • Patient Engagement
  • Pharmaceutics
  • Pricing - Reimbursement
  • Professional Education - Training & Development
  • Project Management
  • Public Policy - Health Care Compliance - Law
  • Public Policy - Law
  • QA-QC
  • Quality Assurance - Quality Control
  • R&D - Strategic Issues
  • Rare - Orphan Diseases
  • Regulatory Affairs
  • Statistics
  • Strategic Planning
  • Study Endpoints
  • Submissions
  • Val - Electronic Info Integrity