Central Laboratories Solutions

31. Rave TSDV - Improve CRA Efficiency And Reduce Site Burden 12/20/2023

    Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.

32. Launch Strategy & Planning 7/27/2021

    Read how IQVIA™ Biotech can help you integrate recent market dynamics and longer-term trends into your launch strategy for a precise understanding of launch risks and expectations.

33. Revvity Signals Software Solutions For Pharmacovigilance And Drug Safety 5/13/2022

    Strategically transform your medical review, safety review, and compliance monitoring processes with our innovative solution for Pharmacovigilance.

34. Unlock The Hidden Value Of Your Data 3/15/2022

    The predictive strength of Study Feasibility’s algorithms is optimized when fed with a sponsor’s own data. Explore how these machine learning models are powered by trial operational metrics, site and investigator performance/quality data, activation timelines, real world data, and more.

     
35. Intelligent Trials: Design and Execute Faster Trials with AI-Powered Insights 11/19/2024

    Explore how Intelligent Trials leverages the industry’s largest clinical dataset to accelerate enrollment, improve diversity, and provide real-time insights, ensuring efficient, data-driven trial success.

36. Vaccine Solution 11/19/2024

    Explore how this unified vaccine solutions platform integrates advanced tools for vaccine trials, offering unified data management that reduces silos, enabling efficient decision-making.

37. A Simplified, Accessible Solution For Phase I And Phase IV Trials 10/23/2024

    Rave Lite is an efficient, cost-effective solution tailored for Phase I and Phase IV clinical trials. This technology simplifies data capture, management, and analysis, enabling accelerated study timelines.

38. GxP Data Integrity: Assessment, Readiness, And Compliance 7/24/2024

    Our team comprises seasoned professionals in life sciences and regulatory compliance, offering tailored solutions for your unique data integrity challenges.

39. Data-Backed Recommendations For Primary Endpoints And I/E Criteria 10/23/2024

    Protocol SmartDesign is a first-of-its-kind solution that uses AI and trusted data to recommend successful trial elements, streamlining planning and accelerating development.

40. Real-World Data And Real-World Evidence 10/15/2025

    As clinical research evolves, RWD and RWE play a crucial role in complementing conventional randomized controlled trials (RCTs) by capturing insights that accurately reflect clinical practice.