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SERVICES
OUR SERVICES
WHAT WE OFFER
At ERD, we perform both full and sub gallery of management functions depending on what your requirements are. These functions are tailored to meet specific trial per site requirements. Our areas of specialty are:
By shouldering these responsibilities, ERD helps to alleviate the burden on researchers and trial site staff, allowing you to focus on the scientific aspects of the trial. We serve as a valuable resource, providing the necessary expertise and support to ensure successful trials.
Identifying and selecting suitable trial sites
With a deep understanding of the research landscape, we are adept at identifying trial sites that meet the specific requirements of each study. We carefully evaluate factors such as site capabilities, patient population, and geographical location to ensure the success of the trial.
Providing training and assistance to site personnel
We recognize the importance of well-trained site personnel in conducting successful clinical trials, hence our offering of comprehensive training programs to ensure that site staff are equipped with the necessary knowledge and skills to carry out their roles effectively.
Managing regulatory compliance
Regulatory compliance is a critical aspect of clinical trials. ERD have in-depth knowledge of the regulatory framework, and we ensure that all necessary approvals and documentation are obtained. We work closely with regulatory authorities to ensure that trials are conducted in accordance with applicable laws and regulations.
Ensuring adherence to Good Clinical Practice (GCP) guidelines
GCP guidelines are a set of international standards that ensure the ethical and scientific integrity of clinical trials. ERD plays a vital role in ensuring that all trial activities at the site adhere to these guidelines, promoting the safety and well-being of trial participants.
Monitoring the progress and quality of trials
We employ a robust monitoring system to track the progress and quality of trials. We conduct regular site visits, review data collection processes, and ensure that all trial activities are carried out in accordance with the study protocol. This proactive approach allows for early identification and resolution of any issues that may arise during the trial.
Coordinating participant recruitment and retention activities
Participant recruitment and retention are crucial for the success of clinical trials. ERD employ various strategies, such as targeted marketing campaigns and patient engagement initiatives, to ensure optimal participant enrollment and retention rates. We work closely with trial sites to develop recruitment plans and implement effective retention strategies.
Ensuring accurate data collection and documentation
Accurate data collection and documentation are essential for the validity and reliability of clinical trial results. We implement robust data management systems to ensure that all data collected during the trial is accurate, complete, and securely stored, as well as providing adequate oversight for the timely submission of required documentation to regulatory authorities.
Offering financial management and budgeting support
ERD provides financial management and budgeting support to ensure that trials are conducted within the allocated budget. We work closely with sponsors to develop comprehensive budgets, monitor expenses, and provide financial reporting throughout the trial.
UNLOCK EXCLUSIVE OFFERS AT EDLAURENCE RESEARCH DYNAMICS AND ADVANCE YOUR HEALTH WITH OUR CUTTING-EDGE BIO PHARMA SOLUTIONS
Contact info@edlaurence.com for any further information you may require or book a consultation with our staff.
TESTIMONIALS
WHAT PEOPLE SAY
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