Our mission is to ensure the generation of accurate and precise findings.
Please enter subscribe form shortcode
Please enter instagram feed shortcode
Data Collection: We employ robust
data collection methods, utilizing both
traditional and electronic data capture
(EDC) systems to gather information
accurately and efficiently.
<stron
Data Entry and Cleaning: Our team
meticulously enters data into secure
databases and performs thorough data
cleaning processes to identify and
resolve discrepancies, ensuring high-
quality data for analysis.
<stron
Data Validation: We manage the
collection, validation, and processing of
clinical trial data, ensuring accuracy,
completeness, and compliance with the
protocol
Quality Assurance: Zepeda Research
implements rigorous quality assurance
measures to maintain the integrity of the
trial data, conducting validations to
ensure data quality and reliability.
Regulatory Compliance:
We specializes in navigating the regulatory
landscape of El Salvador, ensuring
compliance with local regulations and
international standards for clinical
research.
Documentation Support: We provide comprehensive documentation support, assisting clients in preparing and submitting regulatory documents required for clinical trial approval in El Salvador. This includes managing the submissions of protocols and other necessary documents optimizing timelines and minimizing regulatory hurdles to expedite approval processes.
Ongoing Compliance: Zepeda Research conducts ongoing
compliance throughout the duration of
the trial, ensuring that all regulatory
requirements are met and maintained.
We handle all submissions and
regulatory interactions on behalf of our
clients, providing a seamless and
efficient regulatory affairs service.
Patient-Centric Recruitment: With a patient-centric approach, we implement tailored recruitment strategies to attract and retain eligible participants throughout the trial. Our
comprehensive recruitment services
ensure timely enrollment and high
retention rates.
Patient Support Services: We provide
personalized support to enrolled
participants throughout the trial
process, offering assistance with scheduling appointments, transportation logistics, and addressing any concerns or challenges they may encounter.
Retention Strategies: In addition to
recruitment, we implement retention
strategies to maintain participant
engagement and minimize dropout rates. This includes regular communication, and support services to enhance the participant experience and promote trial completion.
Comprehensive Execution: We provide comprehensive execution of clinical trials, overseeing all aspects of trial management including, data
collection, and regulatory compliance.
Quality Assurance: Our team implements rigorous quality assurance measures to maintain the integrity of the trial data and ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements.
Budget management: We efficiently
manage financial resources in clinical trials, following the best practices in budget
management in , we develop strategies to maximize return of investment and we are focused on the importance of transparency and accountability in budget management.