Products and Services

41. Getting Novel Therapies To Patients Everywhere 9/27/2023

    From regulatory pathway selection to patient recruitment challenges to navigating the volume of data to collect and clean — a rare disease therapy requires an extraordinary amount of coordination.

42. Proper Data Management Across All Areas & Phases 7/6/2022

    Get extensive experience developing and delivering quality services for data management departments across all major therapeutic areas and phases for pharma/biotech companies. 

43. Making The Impossible Possible In Oncology And Hematology Clinical Development 9/20/2023

    When the complexities of designing and executing cancer trials in a highly competitive market can mean delays in delivering urgently needed treatments to patients, it pays to have a trusted partner by your side.

44. Clinical And Regulatory Strategy 11/7/2023

    Many biotechnology companies come to Australia to conduct early phase clinical trials and take advantage of straightforward regulatory streams and of the lucrative 43.5% R&D cash refund scheme. Biotechnology companies then often look at locations in Asia, such as South Korea, Thailand and China to tap into their huge treatment-naïve patient populations for their later phase clinical research.

45. Site And Patient Payments 12/5/2025

    With integrations at the heart of our efficiency model, Block Clinical automates payments in three areas: Site Payments, Patient Payments, and Supplier Payments.

46. Commercial Alerts: Now Available With EHR, Claims And Prescription Data 3/27/2025

    Identify & engage healthcare professionals (HCP) treating eligible patients—in near real-time

    Timely physician engagement is critical to therapy adoption. Quest Diagnostics combines near real-time lab data with other data sources including EHR, claims and prescription data to help pharmaceutical teams identify and connect with physicians managing eligible patients at key decision time point in the patient journey.

    In today’s competitive pharmaceutical landscape, ensuring that physicians receive timely, relevant information about new therapies is essential. Quest’s unique combination of industry-leading deidentified lab data, enhanced with claims, prescription (Rx), and EHR insights, allows pharma teams to refine targeting, optimize engagement, and drive better patient outcomes.

47. Medical Writing Software 6/17/2025

    Accelerate Medical Writing Without Compromising Accuracy or Compliance

    In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.

48. Sponsors And CROs 1/13/2026

    Our aim is to ensure the flawless and successful execution of clinical research, maximizing its impact on both patients and the commercial market.

49. Decentralized Trials For Small & Mid-Sized Biotechs 4/28/2021

    We understand how challenging it is to adopt a novel approach to drug development. Pivoting to virtual clinical trials is no exception.

50. Home Trial Support 11/22/2024

    By removing barriers, and bringing trials to patients where they live, we can expand the geographical reach of clinical research across the globe allowing more patients to participate. Our patient-centric delivery means we can create convenience and comfort working the schedule of the trial around the schedule of the patient and their family, not the other way around. This approach provides important access to medical care, enhances the inclusivity of clinical trials and advances drug development for all.