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.
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
Clinical Trial Monitoring
Drug Safety Management
Clinical Data Management
Quality Assurance
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
- Conduct efficient trials
- Follow timelines and Protocols
- Remain cost effective
- Oversee program operations
- Provide scientific expertise
- Facilitate resolution of issues
Therapeutic Experience
- Pediatric
- Rare Diseases
- Oncology
- CNS & CVS
- Dermatology
- Endocrine
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
- Feasibility Studies
- Program Development
- Protocol Development
- Project Management
- Site Management
Other Services
- Site Monitoring
- Safety Reporting
- Medical Writing
- Data Safety Monitoring
- Advisory board planning and coordination
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
- Infrastructure Needs Assessment
- Patient Centric Recruitment
- Protocol Review and Design
Site Analysis
- Site and Patient Identification
- Performance Acuity
- Logistical 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
- Rare Diseases
- Neurology
- Endocrinology
- CVS
- Pediatric
- Dermatology
- Oncology
- Hematology
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)‑810‑5587!