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  CLINBROKERS  

Experts in Clinical Trials

Our Vision

ClinBrokers provides clinical research services that aids and improves the health of children around the world by providing companies and organizations with experienced resources to implement clinical trials for pediatric patients.

Our vision is to eliminate HINDSIGHT, promote INSIGHT to yield the FORESIGHT of a successful clinical trial.

We are experts in Trial, Site, Patient Management, and CTMS, while building Clinical Study Contracts & Budgets, management of SOW and Project Timelines.

Quality Assurance

Be it, 21 CFR, ISO 13485, 14155 or 9000. We regularly perform audits of CRFs/Protocols, TMFs, Sites, Biometrics, Data Management, other Reports and Dossiers for Submissions.

Trial Monitoring

From Initiation, Routine Monitoring to Closeout Visits, we help identify and address Protocol Deviations & Violations, as per GCP/ICH, FDA, EMEA, APAC or LatAM.

Feasibility Studies

Find the right Investigators and subjects, globally. Our team of experts can provide solutions to stalled recruitments and let you achieve milestones even with previously missed timelines.

Safety Management

We provide support in regulatory agency representation, response to subject evaluation criteria questions, while helping you monitor AE and SAEs.

Medical Writing

Our team can compile, organize, write, edit, and produce a wide range of medical and scientific documentation required to support your clinical development programs.

50 Years of Experiences

Leadership

Spearheaded by skilled research professionals with more than 50 years of combined industry experience, our highly devoted functional experts promote a collaborative and transparent environment with oversight for successful and quality study results.

Clinical Trial Management

Our PM team works effectively and meticulously to manage all critical aspects of the trial to ensure on-time delivery of results, within budget and with the highest quality output.

Clinical Trial Monitoring

Our CRAs are highly skilled, therapeutically aligned, trained, and committed to excellence in every study with highest standards of focus towards protecting patient safety, well being, rights and data integrity.

Drug Safety Management

Subject safety and wellbeing is our top priority. Our team of physicians will leverage their clinical experience and practical knowledge in the conduct of a clinical study.

Clinical Data Management

CDM is a critical phase in clinical research, and the integrity of clinical data is of paramount importance. We ensure the integrity by strict adherence to SOPs and review procedures at every stage of the project.

Quality Assurance

We regularly conduct internal process audits to ensure compliance with applicable good clinical practices, standard operating procedures, vendor qualifications, and commitments to clients – all of these are for the purpose of consistently ensuring the quality of our services remains at the highest level.

How We Do It

We partner with our clients to employ creative mechanisms to allow us to methodically produce fast, efficient and quality results. We provide the clinical options; you choose the solutions!

Global Clinical Trial Operations

Children are the future of our planet.  Getting them healthy is our goal. As a trusted partner, we bring our expertise and attention to this cause. This is especially true in pediatrics, where a defenseless patient population requires the skills of our subject-matter experts.  ClinBrokers is a specialty provider with the capabilities and expertise to support clinical trial operations from conception to finalization.

Capabilities

Therapeutic Experience

Range of Services

We at ClinBrokers offer a broad range of Clinical Trial Services from Phase I, IIB, III to IV for Pharmaceutical, Biotechnology and Medical Devices to bring new drugs and devices to global reach faster. We also extend our services to growing areas like Gene Therapy and Neutraceuticals.

With a strong experience of conducting clinical trials, ClinBrokers has the global reach and capability to conduct clinical studies and navigate through regulatory requirements for Investigational New Drugs (INDs), Abbreviated New Drug Applications (ANDAs), WHO and various Local regulatory agencies.

Our Speciality

Other Services

WE PROVIDE

Solutions

From Global clinical trial solutions to Feasibility Studies, we walk you through each step of a clinical trial. If you are troubled by your current teams' performance and are not achieving required milestones, we can make your study succeed as a Rescue Mission.

Backed by strong clinical and therapeutic expertise, we take a highly flexible and customized approach to clinical research by listening closely to our customers and tailoring our services to their unique needs and projects.

Clinical Trial Feasibility

The key to a successful trial begins in the feasibility stage. Gathering the right data for site selection and patient recruitment is an extremely important task. We promote insightful information which would aid in finalizing the ultimate site selection list, thus enhancing the patient recruitment process.

This should not only be considered a beginning task, but has proven most effective when conducted throughout the recruitment phase, be it in the initiation phase or as a Rescue Mission.

Feasibility Solutions

Site Analysis

Rescue Studies

When your study is in trouble, help us bring your study back into balance. We have rescued more than a dozen clinical trials while remaining patient focused.

Our experience includes rescue studies in phases I through IV over the past decade. We offer, increased flexibility and efficiency, we can follow your SOPs or provide our own, or amend it to a new version to accommodate your study. We will create and manage a rescue study or trial optimization plan that meets your clinical trial needs.

As a Feasibility Rescue Mission, we’ve been able to augment and increase recruitment by up to 70%.

Rescue Study Experience

Learning Center

One way to reduce barriers to health care access and enable everyone to benefit from new medicines is to ensure that clinical trials are safe, diverse and inclusive, while including participants from a population where the medicine intends to be introduced and delivered. We continue to publish updates about clinical trials and health safety. Subscribe to our blog to know more!

    Contact us

    Ask yourself the following:

    • Has your recruitment been stalled?
    • Do you find it difficult to find the right Investigators and subjects, globally?
    • Are you missing timelines because the patient population is lacking?

    If you answered 'yes' to any of those questions then you need our team of experts to provide solutions!  So, save your budget and call us now (919)8105587!