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Archives for Lisa Pahl
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Page 9
Author:
Lisa Pahl
Tags
Clinical Trial Data Sharing: Medical Affairs’ Role
Message to Clients – COVID-19
When a Direct-to-Patient Trial Model Is the Right Choice
How To Prevent Systemic Bias in Clinical Trials
Top 2020 Conferences CROs Should Not Miss
10 Global Medical Affairs Conferences to Attend in 2020
INSIGHTS from ISMPP EU
SCOPE Summit 2020: Anju’s eClinical Solutions
Global Clinical Trials: Managing Patients and Meeting Compliance
Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
2020 European Meeting of ISMPP: Achieving Clarity, Reach and Value
Does Your Clinical Trial Need a Chief Patient Experience Officer?
How Medical Affairs Teams Can Help Get Off-Label Drugs to Patients
Anju Featured in CIO Review
Virtual Reality in Clinical Research: Potential and Challenges
How Medical Affairs Can Use Tech to Provide Medical Information Letters
INSIGHTS from DIA 2019 MICC
Experimental Design: New Therapies Are Being Developed to Treat Lifelong Illness
FGK Clinical Research Signs Five-Year Agreement with OmniComm
IRTMaster by OmniComm: Accelerating Trial Development
Insights from ISMPP WEST 2019
Best Practices for Managing Phase Transition in Adaptive Trials
DIA Medical Information and Communications Conference
Understanding FDA 483: How To Run a Compliant Trial Every Time
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