Digital Site Suite OG

  1. Trends In Sponsor-Of-Choice Initiatives: Consolidating Site Payments 5/5/2023

    Listen in as leaders from Bristol Myers Squibb, CenExel Centers of Excellence, and IQVIA Technologies discuss the importance of providing a consistent clinical trial payment experience to sites.

  2. Using IRT Data To Automate And Optimize Clinical Supply 4/17/2023

    Learn how clinical teams can save between $150,000 and $1 million in annual drug and shipping costs through automated supply optimization.

  3. Providing Drug Supply Support In Complex Environments Through IRT 4/5/2023

    Learn how applying predictive data analytics can enable the creation of an ideal supply strategy capable of reducing the need for extra shipments, manual oversight, and supply waste.

  4. Pharma's Frozen Assets 4/18/2023

    Delve into a data-driven approach to assess the volume and value of cold chain medicines by combining IQVIA audit data with publicly available data.

  5. The IQVIA Investigator Site Portal 11/15/2022

    Understand why companies are standardizing operations on a purpose-built, proven platform that empowers sites to succeed and provides sponsors with helpful insights.

  6. Advanced Tech Can Thwart Site Staffing Problems 7/6/2022

    In clinical research, staffing shortages can delay trials and prevent new therapies from getting to patients in need. Read why Melissa Easy, VP, Clinical Technologies at IQVIA, believes advanced tech may bridge this gap as she reviews tools that are proving useful to study teams.

  7. 3 Key Functions Your eTMF Needs To Meet New EMA Regulations 6/23/2022

    The European Union Clinical Trial Regulation No. 536/2014 recently introduced the most significant changes to the processes for clinical trial applications in at least the past 15 years. Learn how this impacts the Trial Master File and consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.

  8. Orchestrated Study Start-Up 10/16/2023

    Learn how the IQVIA Investigator Site Portal reduces activation timelines and eliminates site frustrations by automating processes and providing complete oversight to study teams.

  9. IQVIA eArchive 5/21/2021

    Whether you’re archiving a TMF delivered by your CRO partner, looking to move out of noncompliant file systems, or interested in reducing the high costs of archiving in your active eTMF, IQVIA eArchive is the rapid deployment solution for you.

  10. Alnylam Puts Sites And Patients First With IQVIA Technologies Investigator Site Portal

    When Alnylam Pharmaceuticals began developing medicines for rare diseases with few or no treatment options, the company’s leaders knew they needed to design clinical trials that kept patient well-being and disease burden at the forefront.