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Frequently Asked Questions

What is a Clinical Research Organization (CRO)?

A Clinical Research Organization (CRO) is a service provider that supports pharmaceutical, biotechnology, and medical device companies in conducting clinical trials. CROs handle various aspects of the clinical trial process, such as study design, project management, patient recruitment, regulatory submissions, data management, and more. By partnering with a CRO like Conduct Research, companies can efficiently execute clinical studies while focusing on their core innovations.

What services does Conduct Research provide?

Conduct Research offers a comprehensive range of clinical research services, including:

  • Study Design & Planning
  • Clinical Trial Phases Supported
  • Project Management
  • Regulatory Affairs Support
  • Patient Engagement & Retention
  • Clinical Trial Monitoring 
  • Quality Assurance

Our team is skilled in managing trials across all phases (Phase I-IV) and specializes in oncology research, allowing us to support clients from early-stage testing to post-market surveillance.

How does Conduct Research ensure compliance with regulatory standards?

Compliance with regulatory requirements is a top priority for Conduct Research. We strictly adhere to Good Clinical Practice (GCP) guidelines and stay up-to-date with regulations from Health Canada, the FDA, EMA, and other global regulatory bodies. Our experienced regulatory affairs team guides clients through each regulatory process, ensuring that all submissions are thorough, accurate, and timely to minimize delays.

What types of clinical trials does Conduct Research support?

Conduct Research provides support for all phases of clinical trials, including:

  • Phase I: Early-stage, small-scale trials to assess safety and dosage
  • Phase II: Studies to evaluate effectiveness and further assess safety
  • Phase III: Large-scale trials to confirm efficacy and monitor adverse effects
  • Phase IV: Post-market studies to gather additional information on treatment use in broader populations

Our expertise in oncology makes us a valuable partner for clients seeking specialized knowledge and guidance in this complex therapeutic area.

How does Conduct Research recruit and retain patients for clinical trials?

Patient recruitment and retention are key to the success of any clinical trial.

Conduct Research uses a variety of strategies to identify and engage eligible participants, including partnerships with healthcare providers, targeted outreach campaigns, and patient advocacy networks. Once enrolled, we prioritize patient engagement through consistent communication, support resources, and follow-up to ensure a positive experience and encourage continued participation.

Why should we choose Conduct Research as our CRO partner?

Conduct Research combines deep industry expertise with a commitment to quality, compliance, and patient care. We offer end-to-end clinical trial services with a patient-centric approach, ensuring that every aspect of the trial is conducted with the highest standards. Our personalized, flexible solutions and robust project management capabilities make us a trusted partner for companies of all sizes. For more details on why we stand out, visit our Why Us page.

What therapeutic areas does Conduct Research specialize in?

While Conduct Research can support in a range of therapeutic research areas, Oncology remains our primary speciality.

Our team has extensive experience in managing the unique challenges of oncology trials, from patient recruitment to complex regulatory requirements. This focus allows us to provide a higher level of support and expertise for oncology-related studies.

What is the process for starting a clinical trial with Conduct Research?

Starting a clinical trial with Conduct Research involves several key steps:

  1. Consultation: We begin with a thorough discussion to understand your study requirements, goals, and timeline.
  2. Study Design & Planning: Our team assists with protocol development, feasibility studies, and budget planning.
  3. Regulatory Approvals: We handle regulatory submissions to ensure compliance.
  4. Project Launch: Our project management team oversees the trial’s execution, from site selection to patient recruitment and data collection.
  5. Ongoing Monitoring: We conduct regular monitoring and quality assurance to maintain the integrity of the study.
  6. Reporting and Analysis: At the end of the trial, we provide comprehensive data analysis and a final report.

Please contact us for a personalized consultation to discuss your specific needs.

How do you ensure patient safety during clinical trials?

Patient safety is paramount at Conduct Research. We adhere to rigorous protocols and Good Clinical Practice (GCP) guidelines to protect the well-being of participants. Our team closely monitors patients throughout the trial and maintains open lines of communication to address any concerns promptly. Additionally, we work with experienced medical professionals who provide oversight and ensure that all procedures prioritize patient health and safety.