Insights On Clinical Technologies

51. Regulatory Approval For Novel Device Achieved With Comprehensive Clinical Data Management 9/21/2022

    Find out how data capture and management activities, programming, and medical writing for a clinical study report were supported to solve the major diagnostic challenge of distinguishing between bacterial and viral infections.

52. The Future Of Work In Clinical Research 7/27/2022

    In this report, Advarra explores what the "next normal" will be for clinical research organizations following the COVID-19 pandemic. 

53. Language Landscape: Latin America 2/10/2022

    As Latin America (LATAM) is becoming a key market for pharmaceutical companies, the need to connect with the patient population there has increased as well. Decide whether or not translating your content from English to Spanish LATAM is the right approach in the available blog.

54. Why Your eTMF Needs Role-Based Access 3/2/2023

    Discover how role-based access controls can offer a way for clinical teams to answer the tough questions from regulators, investors, and other parties.

55. Your Treatment Plan For Curing The App Localization Headache 3/17/2022

    App localization is the process of adapting apps and their content to another language in a conceptually equivalent and culturally appropriate way. This article tackles how to treat the hurdles that comes from this process.

56. How To Build A Successful, Decentralized Clinical Trial And Avoid Common Mistakes 10/25/2021

    The process of decentralizing a clinical trial can be complicated, especially when the industry is accustomed to the “tried and true” approach. In this article, learn about the critical planning considerations needed to incorporate decentralization in your next trial.

57. Fast, Focused Medical Data Review: Use Cases By A Medical Monitor 11/30/2021

    For medical monitors, the problem with off-the-shelf analytics tools is the lack of tailoring for medical review needs. The right data visualization tool can help medical monitors to tailor and improve their data review processes and enhance their ability to identify safety signals both quickly and surely.

58. Safeguarding Trial Data Privacy In Remote Environments 11/15/2022

    As clinical trial sponsors and CROs digitally transform themselves to better serve a post-pandemic world, learn why a primary focus is on how to safely transfer information among remote environments to keep trial data confidential and compliant.

59. Prevent Patient Recruitment And Retention Issues With Digital Connections 9/16/2022

    This article covers  what the “patient experience” is in clinical trials, the problems with the patient experience in clinical trials, and four ways digital connections can create a positive patient experience in clinical trials.

60. COVID-19: The Catalyst For Change 6/2/2021

    The modern and highly regulated clinical trial industry has never faced a pandemic of this magnitude, and trial continuation is critical when patients’ lives are in the balance. The FDA has approved and encouraged the use of eSource since 2013, but some were still resistant to adopting virtual protocols. Will COVID-19 be the catalyst to following the FDA guidelines on decentralized and virtual trials?