Your Trusted Clinical Research Organization in Edmonton, Canada
Introduction
Welcome to Conduct Research, a leading Clinical Research Organization (CRO) based in the vibrant city of Edmonton, Canada. We are dedicated to providing comprehensive and efficient solutions for all stages of the clinical research process. With our expertise, experience, and commitment to excellence, we serve as a trusted partner for pharmaceutical companies, biotech firms, medical device manufacturers, and academic institutions worldwide.
Quality is of utmost importance to us. We adhere to stringent quality standards to ensure that every aspect of the clinical trial is conducted with precision and accuracy. From study design and planning to data management and analysis, we prioritize quality at every step. By upholding the highest standards of quality, we strive to generate reliable and meaningful results that contribute to evidence-based decision-making and improve patient outcomes.
Compliance is a core principle that guides our operations. We strictly adhere to regulatory requirements, industry guidelines, and ethical standards. Our team of experts remains updated with the latest regulations and ensures that all aspects of the clinical trial align with the applicable guidelines and Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Good Laboratory Practice (GLP). By prioritizing compliance, we provide our clients with the assurance that their studies are conducted ethically and in accordance with the highest standards of integrity.
Innovation is at the heart of our mission. We strive to drive innovation in clinical research by introducing novel approaches, technologies, and methodologies. Our team of experienced professionals remains at the forefront of industry advancements, ensuring that we incorporate the latest developments into our services. By embracing innovation, we aim to enhance the efficiency, accuracy, and effectiveness of clinical trials, ultimately making a positive impact on healthcare outcomes and improving patient care.
At Conduct Research, we are passionate about the advancement of medical knowledge and the improvement of patient care. Through our focus on quality, compliance, patient-centricity, and innovation, we are dedicated to making a lasting impact on the field of clinical research. Join us in our mission to drive scientific progress, improve healthcare outcomes, and shape a better future for patients worldwide.
Our Services
Study Design and Planning
At Conduct Research, we understand the critical importance of a well-designed study for achieving meaningful and reliable results. We collaborate closely with our clients to develop robust study designs and comprehensive research plans tailored to their specific objectives. Our experienced team of researchers, clinicians, and statisticians brings their expertise to the table, ensuring that your study design is scientifically sound, adheres to regulatory requirements, and maximizes the potential for success. By considering factors such as sample size, study endpoints, data collection methods, and statistical analysis, we lay the foundation for a study that generates high-quality data and valuable insights.
Regulatory Affairs
Navigating the complex landscape of FDA, Health Canada, EU, ICH-GCP, and local regulatory requirements is a crucial aspect of clinical research, and it requires in-depth knowledge and expertise. At Conduct Research, our regulatory affairs experts team are well-versed in the ever-evolving regulatory landscape. We will guide you through the entire regulatory process, providing comprehensive support in preparing and submitting regulatory documents, ensuring compliance with applicable laws and regulations, and facilitating interactions with regulatory authorities. By keeping abreast of the latest regulations, guidelines, and ethical standards, we help streamline the regulatory pathway,This savesing you time while and ensuring that your study remains compliant and in good standing.
Patient Recruitment and Retention
Successful patient recruitment and retention are critical for the timely completion of clinical trials. At Conduct Research, we employ targeted strategies and innovative approaches to identify and engage eligible participants. We understand that patient well-being and ethical treatment are paramount, and we prioritize building trust and maintaining open communication with participants. Our patient-centric initiatives focus on providing a positive experience for study participants, maximizing enrollment, and minimizing dropouts. By leveraging various recruitment channels, implementing personalized engagement strategies, and prioritizing participant needs, we help ensure the success of your study by maintaining high participation rates and reducing the risk of data bias.
Data Management and Biostatistics
Accurate and reliable data is the cornerstone of meaningful research outcomes. At Conduct Research, our data management experts employ advanced technologies and robust processes to ensure secure and efficient data collection, storage, and analysis. We implement data management systems that adhere to industry best practices, maintaining the confidentiality and integrity of study data. Our biostatisticians provide expertise in statistical analysis, ensuring that your study results are appropriately interpreted and support evidence-based decision-making. By applying rigorous statistical methods, we help you derive meaningful insights from your data and draw reliable conclusions.
Quality Assurance and Compliance
Quality and compliance are non-negotiable aspects of our operations at Conduct Research. We maintain the highest standards of quality throughout every step of the clinical research process. Our quality assurance team conducts comprehensive audits and inspections to ensure adherence to regulatory guidelines, protocol compliance, and data integrity. By continuously monitoring and improving our processes, we identify areas for enhancement and implement measures to deliver reliable and high-quality results. Our commitment to quality assurance and compliance provides you with the confidence that your study is conducted with the utmost integrity and in accordance with industry standards and regulations.
In summary, Conduct Research offers a comprehensive suite of services to support your clinical research endeavors. From study design and planning to regulatory affairs, site management, patient recruitment and retention, data management and biostatistics, and quality assurance and compliance, we have the expertise and resources to optimize the success of your clinical trial. Trust Conduct Research as your partner in driving scientific advancement, ensuring regulatory compliance, and delivering high-quality results. Together, let's make a significant impact on healthcare outcomes and contribute to the advancement of medical knowledge.