Frequently Asked Questions
Below you’ll find answers to some of the most frequently asked questions at Mprex. We are adding the most asked question to this page so if you have a question and don’t see your answer, don’t hesitate to email us at clinicalresearch@mprex.in
We offer a comprehensive range of services including protocol development, site selection, patient recruitment, regulatory compliance, data management, monitoring, and reporting.
Our team comprises experienced professionals with expertise in various therapeutic areas and extensive experience in managing and conducting clinical trials according to international standards and regulations.
Patient safety is our top priority. We adhere strictly to ethical principles an regulatory guidelines, conduct thorough risk assessments, implement robust safety monitoring procedures, and provide appropriate training to all staff involved.
We employ a targeted and multi-faceted approach to patient recruitment, utilizing various channels including social media, patient databases, healthcare providers, and community outreach programs to ensure timely enrollment of suitable participants.
We implement stringent quality control measures throughout the trial process, including data validation checks, source document verification, and regular monitoring visits to ensure data accuracy, completeness, and integrity.
We have a proven track record of successfully meeting project timelines and budgets, thanks to our efficient project management practices, proactive risk management, and flexible resource allocation strategies.
Yes, we provide comprehensive support for regulatory submissions and approvals, including preparation of regulatory documents, interactions with regulatory authorities, and compliance with local and international regulations.
We adhere strictly to ethical principles and regulatory requirements, including Good Clinical Practice (GCP) guidelines, ensuring that all aspects of the trial are conducted ethically and in accordance with applicable laws and regulations.
Yes, we offer post-trial support services including data analysis, interpretation of results, preparation of final reports, and assistance with manuscript writing and publication.
Our CRO stands out for its commitment to excellence, scientific rigor, flexibility, and client-centric approach. We prioritize building long-term partnerships with our clients and strive to deliver exceptional results with every project.