eyeforpharma Value Summit 2018
November 07, 2018 - November 08, 2018
Philadelphia, PA (USA)
ARE YOU KEEPING PACE?
From the latest in real-world evidence generation, to expert insights navigating the complex payer landscape.
We will have PAREXEL representatives at the event that can talk to you about how we can translate robust market access expertise and research acumen into insightful and actionable access and evidence generation strategies.
Click below to book your slot for a discussion of your needs.
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Presentation
November 7, 2018
Advancing the use of RWE – What progress have we made? Where can we go next?
Camie Britton
Senior Director, Medical & Scientific Services
Visit the eyeforpharma Value Summit website
for presentation details.
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2018
Products and Services
- DIA Pharmacovigilance and Risk Management Strategies 2018
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - New Jersey
- Campus Event China – Sun Yat-sen University
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - San Diego, California
- EU ISMPP
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - North Carolina
- Campus Event China – Southern Medical University
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - San Francisco, California
- DIA Regulatory Submissions, Information and Document Management
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - Illinois
- Campus Event China – China Medical University
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - Seattle, Washington
- Arena Clinical Trial Supply Europe
- NAVIGATING THE CHINESE REGULATORY LANDSCAPE: KEY CONSIDERATIONS FOR ACHIEVING FAST TRACK APPROVALS IN A RAPIDLY DEVELOPING MARKET - Los Angeles, California
- AMWA Medical Writing & Communication Conference
- FDLI - Enforcement, Litigation and Compliance Conference: For the Drug, Device, Food, and Tobacco Industries
- American Society for Clinical Pharmacology and Therapeutics (ASCPT)
- 3rd Advanced GMP Workshops 2018
- Informa eRegulatory Summit
- Partnerships in Clinical Trials (PCT) 2018
- Terrapinn World Orphan Drug Congress US
- IDDST-China
- ISMPP
- Arena Outsourcing in Clinical Trials East
- ISPOR Annual US
- ASCO
- DIA Annual Conference
- Generating Evidence for Successful Market Access Symposia
- ISCR Annual Meeting 2018
- Medical Affairs Leaders Forum Spring
- BIO Korea 2018
- eyeforpharma Medical Affairs 2018
- EyeforPharma Medical Affairs USA
- DIA China 2018
- STEM Networking Event
- Global Clinical Trials Connect 2018
- Graduate Open House Event Nottingham
- Arena OCT West Coast
- "The Art and Science of Productive FDA Meetings - JLABS Bay Area "
- The Conference Forum - Immuno-Oncology 360
- Global Cancer Immunotherapy Summit
- Nottingham Trent University - eNGage Series
- IQPC Clinical Trial Supply Forum
- MAPS 2018 Annual Meeting (Medical Affairs Professional Society)
- ASCO-SITC Clinical Immuno-Oncology Symposium
- Brunel University London Careers Fair
- Medical Statistics Taster Day 2018
- PAREXEL MassBio Lunch & Learn
- Recruiters in Residence - University of Birmingham
- BioTech Pharma Summit: Biosimilars & Biologics 2018
- University of Nottingham (Jubilee campus)
- PhUSE US Connect 2018
- ACRP 2018 Annual Conference
- NAVIGATE UPDATED EU GUIDELINES ON RISK MITIGATION FOR FIH & EARLY CLINICAL TRIALS - Frankfurt, Germany
- NAVIGATE UPDATED EU GUIDELINES ON RISK MITIGATION FOR FIH & EARLY CLINICAL TRIALS - Munich, Germany
- Global Clinical Supplies Group (GCSG) Conference
- PhUSE 2018 Single Day Event in Poland
- DIA EuroMeeting
- 16th Annual Congress of International Drug Discovery Science and Technology (IDDST-2018)
- ACRP CRA Virtual Career Fair
- The Art and Science of Productive FDA Meetings
- The Art and Science of Productive FDA Meetings
- PharmAccess Leaders Forum
- The Annual Conference for the Advancement of Clinical Research in Israel 2018 by CTrials and Pharma Israel
- PAREXEL MassBio Lunch & Learn
- Free Webinar: PAREXEL's Next Generation of CRAs in France
- ISPE COP Investigational Products: Insights into driving Trends and Technology in Clinical Supply Chain
- DIA 2018 Preview Party
- The Art and Science of Productive FDA Meetings
- Euro Biosimilars 2018
- Real-World Evidence & Access Europe 2018
- EMWA 2018
- PAREXEL INTERNATIONAL FRANCE, SYMPOSIUM SESSION
- Free Webinar: PAREXEL's Next Generation of CRAs in Italy
- Medical Communications Virtual Career Fair
- Maximizing value for emerging BioPharma companies
- Boston Career Forum 2018
- What, Why, Where, When and How to hold your first First-In-Human trial
- Virtual Career Fair – CRAs and Oncology Clinicians
- DPharm: Disruptive Innovations
- Early Phase Regulatory Affairs and Clinical Study Design Consideration
- SCDM
- Arena Outsourcing in Clinical Trials Southern CA
- SCRS
- Outsourcing & Supply Chain - A 360° View
- RAPS
- ISPOR 21st Annual European Congress
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - London
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Stockholm
- CBI IRT
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Copenhagen
- Campus Event China – Shenyang Pharmaceutical University
- Medidata NEXT
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Amsterdam
- Campus Event China – China Pharmaceutical University
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Frankfurt
- HORIZONS
- eyeforpharma Value Summit 2018
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Munich
- GRAS - Global Regulatory Affairs Summit
- Adaptive Trial Designs: Maximizing the Opportunity for Success in Drug Development
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Paris
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Milan
- Navigating the Chinese regulatory landscape: Key considerations for achieving fast track approvals in a rapidly developing market - Basel
- The road to drug development: How to strategically navigate commercialization to achieve long-term success
- ISCR - Medical Writing
- What, Why, Where, When and How to hold your first First-In-Human trial? …and other important clinical trial answers
- 11th Edition PHARMACCESS Leaders Forum
- Spotlight on Placements - Sheffield Hallam