Data Management
Study Startup Success for BioPharma and MedTech: Engage a Research Compliance Partner
Engaging with an expert research compliance partner throughout the clinical development process allows researchers to focus on what matters
James Riddle and Luke Gelinas Explore Digital Health and Regulation
This podcast covers an array of topics as they explore how COVID has been a catalyst for change, what digital health means for running clinical trials, and how sponsors, CROs, sites, and IRBs can consider when reviewing new digital technologies as a result of COVID.
How Staff Augmentation Assists with Successful Data Migration
With the goal to move active data from one system into OnCore CTMS, Advarra’s Staff Augmentation team worked with a customer’s associated hospital as it was faced with software termination.
Key Considerations for Regulatory Compliant Document Storage
It is imperative that your organization has a reliable eRegulatory system and associated policies for storage and upkeep of clinical trial documents to ensure 21 CFR Part 11 compliance. Read our Key Considerations for Regulatory Compliant Document Storage.
Wayne State University Streamlines Compliance with Validation Services for Advarra EDC
By the Numbers: Our Response to COVID-19
We are honored to support a resilient research community during the COVID-19 pandemic. Explore our resources to find out how we keep research moving forward.
Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials
Learn more about the importance of medical coding dictionaries, their common uses, and best practices.
Advarra EDC Validation Packet Overview
The validation subscription provides your organization with the resources to optimize validation of your Advarra EDC instance.
Six Key GDPR Questions to Review
Questions still remain about GDPR and its applications. Have you considered these six key questions to ask within your organization?
The GDPR and Its Impact on the Clinical Research Community (Including Non-EU Researchers)
Please note that this material is provided for informational purposes only and not for the purpose of providing legal advice.
Data Collection in Clinical Trials: 4 Steps for Creating an SOP
Learn the necessary steps to create an effective SOP for data collection in clinical trials when using an electronic data capture (EDC) system.
Beginner’s Guide to an Electronic Data Capture (EDC) System
An Electronic Data Capture system stores patient data collected in clinical trials. Learn the basics & functionality of EDC systems.
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