About EloquiMed
Founded by seasoned medical writers and regulatory experts, EloquiMed provides high-quality clinical and regulatory documentation services to pharmaceutical and biotech organizations worldwide.
Our Mission
Our mission is to empower pharmaceutical and biotech organizations through exceptional medical writing and expert regulatory consultation, helping transform innovative ideas into approved medicines that improve patients' lives.
EloquiMed is pioneering a new approach to medical and regulatory documentation that combines deep scientific expertise with cutting-edge technologies. We apply rigorous methodologies to transform complex clinical data into clear, compliant, and compelling narratives that accelerate the regulatory approval process.
Our proprietary AI-assisted workflows streamline document creation while maintaining the highest standards of scientific accuracy. By leveraging natural language processing and machine learning technologies, we reduce documentation time by up to 40% while enhancing consistency, quality, and compliance across large document portfolios. This enables our expert writers to focus on higher-level strategic elements that require human expertise.
Our approach integrates advanced document management systems, automated quality checks, and standardized templates that ensure ICH-GCP compliance, consistent terminology, and adherence to regulatory guidelines across different regions. We employ validated tools for data visualization, statistical analysis interpretation, and cross-referencing to maintain document integrity throughout the development lifecycle.
Through our innovative hybrid approach combining human expertise with technological advancement, we're redefining industry standards for medical writing. Our collaborative model integrates seamlessly with client teams, providing transparency through real-time document tracking, stakeholder review coordination, and milestone-based delivery systems—ensuring critical submission deadlines are consistently met with high-quality documentation.
Our Core Values
The principles that guide our work and relationships.
We maintain the highest standards of scientific accuracy and objectivity in all our work.
We stay current with evolving regulatory requirements to ensure compliant documentation.
We work as an extension of your team with transparent communication and collaboration.
We implement rigorous quality control processes to ensure excellence in every deliverable.
Global Impact
Making a difference in healthcare innovation worldwide through excellence in medical documentation.
EloquiMed has established itself as a global leader in medical writing and regulatory documentation, supporting healthcare innovations across six continents. Our work has contributed to the successful development and approval of numerous breakthrough therapies, from rare disease treatments to novel oncology interventions.
Through our commitment to scientific excellence and regulatory compliance, we've helped accelerate the approval of life-saving treatments, reducing the time from clinical development to patient access. Our global team of experts brings diverse perspectives and deep therapeutic area knowledge to every project.
Beyond documentation, we actively contribute to the advancement of medical writing standards through industry leadership, educational initiatives, and thought leadership in emerging areas such as AI-enhanced medical writing and digital health technologies.
Global Reach
Supporting clients in several countries with regulatory submissions across major health authorities
Therapeutic Expertise
Deep experience across many therapeutic areas, from rare diseases to complex oncology indications
Industry Leadership
Active participation in key industry organizations and contribution to medical writing standards
EloquiMed by the Numbers
Our impact in the pharmaceutical and biotech industry.
Years in Business
Supporting clients since 2010
Clients Served
From startups to global pharma
Successful Submissions
Across FDA, EMA, and other agencies
Expert Writers
PhD and MD-level specialists
Our Approach
How we deliver exceptional value to our clients.
Deep Scientific Understanding
Our teams are led by subject matter experts with advanced degrees in relevant scientific fields, ensuring accurate and insightful documentation.
Regulatory Strategy Integration
We don't just write documents; we ensure they support your overall regulatory strategy and development goals.
Customized Solutions
Every client and project is unique. We tailor our services to your specific needs, timeline, and budget.
Quality Management System
Our comprehensive QMS ensures consistent quality through standardized processes, multiple review levels, and continuous improvement.
Certifications & Affiliations
Our commitment to excellence is reflected in our professional certifications and industry affiliations.
American Medical Writers Association
European Medical Writers Association
Drug Information Association
Ready to work with our expert team?
Contact us today to discuss how EloquiMed can support your medical writing and regulatory needs.