Insight Pharma

Clinical Trials

Clinical trials are research studies that explore whether a medical strategy, treatment, or device is safe and effective for humans. It is a prospective, biomedical or behavioral research study of human subjects that is designed to answer specific questions about biomedical or behavioral interventions (drugs, biologics, treatments, devices, or new ways of using known drugs, biologics, treatments, or devices) in which people volunteer to test new treatments, interventions or tests as a means to prevent, detect, treat or manage various diseases or medical conditions.

These studies also show which medical approaches work best for certain illnesses or groups of people. Clinical trials produce the best data available for health care decision making. Clinical trials are used to determine whether new biomedical or behavioral interventions are safe, efficacious, and effective. IBRSoluTions is providing various types of services in clinical trials helping clients better understand competition, sourcing and trial location etc.

IBRSoluTions provides the following Clinical Trials Services:

Clinical Trials Services
  • Clinical Trials Intelligence

  • Trials Location Mapping

  • Clinical Investigator Intelligence

Clinical Trials Intelligence

  • Clinical trial intelligence is required to optimize clinical trials, decrease time to market, accelerate clinical trial development and maximize portfolio strategies for professionals in clinical operations and development, R&D benchmarking, R&D strategy, strategic resourcing, precision and translational medicine and at contract research organizations (CROs). But searching through regulatory sites and multiple databases, compiling all the information, analyzing and interpreting the trials, is time-consuming. We provide clinical trial intelligence on global clinical trials research, covering a wide range of therapy areas and indications. Our Clinical Trials Intelligence provides you with the information needed to evaluate market opportunities, identify potential barriers, and make better informed decisions regarding clinical trial design and operations.

    IBRSoluTion’s clinical trial intelligence is compiled by experts on trials conducted all over the globe and in various phases of development, with data crossed-checked with key registries, conferences, associations, journals, press releases, literature articles, drug development articles, meeting abstracts, conference reports, and analyst and investor meeting transcripts. We consolidate disparate data streams from tens of thousands of information into a streamlined user friendly intelligence report with extremely detailed criteria like therapy, indication, country, study type, stage of development, status, endpoints, sponsor and collaborator. We ensure our intelligence report is complete, accurate and offers the latest intelligence on global drug development activity. Our intelligence report provides a detailed review of each clinical study including key dates, status, phase, design, location, patient segment, endpoints, subject characteristics, treatments, and results as well as a timeline of key trial events, a summary of study finding in terms of efficacy, tolerability, and adverse events for randomized controlled trials and links to original source material. We enable our clients to take meaningful decision through our clinical trial intelligence like:
    Identifying clinical trials impacting your business
    Evaluating key study messages emerging from clinical studies
    Discovering trials reporting new and important clinical evidence
    Assessing the progress of competitor studies
    Uncovering clinical evidence presented at recent meetings
    Mapping out where clinical trials are being conducted
    Providing reports with easily understandable and presentable form

Trials Location Mapping

  • Site identification is an important component of clinical trials and has a critical impact on subsequent trial timelines, as well as site relationships. To achieve the objective for a successful clinical trial, trial site or location where all the trial related activities are actually conducted has its own importance. A trial site should ensure the safety and confidentiality of the trial subjects, adequate equipments/facilities for subjects, product storage, laboratory assay and the most critical, retention of the information regarding trial subjects; trial documents especially Sponsor/CRO documents.

    IBRSoluTions provides trials location mapping services helping clients to refine the site selection process to identify high-quality sites with proven track records for meeting enrollment goals. Our trials location mapping services empowers our clients to identify:
    • Country offering collaborative contract proposals for conducting clinical trials
    • Destinations having the best economical centers for multi-center clinical trials
    • Best sites for the indication under investigation
    • High enrolling and high performing sites

Clinical Investigator Intelligence

  • A clinical investigator involved in a clinical trial is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. Investigator is the key person who drives the trial from funding location, establishing agreements with sponsors and medical centers, successful patient enrollments with informed consent agreements till successful completion of clinical trial.

    IBRSoluTions provides clinical Investigator Intelligence service helping Pharma/Biotech companies or organizations to select a team of highly experienced and hard working investigators for their clinical trials. We also help our clients in negotiation for agreement with investigators.

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