At HRIG, we offer specialized services to enable efficient, compliant and ethical health research in the Philippines. Each service is designed to provide operational excellence and strategic support for clinical trials and research initiatives.
HRIG provides comprehensive support in developing or upgrading Clinical Trial Units (CTUs). This includes feasibility assessments, categorization of institutional capabilities and creating infrastructure for storage, patient tracking, ethics coordination and data management.
Example: HRIG partners with tertiary hospitals to create plug-and-play CTUs—ready-to-use spaces equipped with compliant systems, reducing administrative burdens and ensuring rapid trial initiation.
We assess hospital readiness through competency evaluations and build-up plans. HRIG coordinates shared research facilities for institutions with limited resources.
Example: A hospital can be transformed into a trial-ready site through HRIG’s tailored readiness program, enabling participation in multi-site vaccine trials.
HRIG offers seamless services for clinical trials, including ethics submission, regulatory liaison, pharmacy coordination, data handling, and monitoring, ensuring that clinical trials are conducted efficiently.
Example: For a cardiology study, HRIG shall manage the entire lifecycle from ethics approval to final monitoring, reducing delays by 30%.
Community engagement ensures smooth recruitment and retention. HRIG implements education campaigns and builds trust among participants.
Example: In rural areas/urban communities, HRIG’s community programs aim to increase enrollment rates for studies.
We provide Good Clinical Practice (GCP) and related research training to ensure investigators and staff adhere to ethical and quality standards.
Example: HRIG shall conduct hybrid GCP training for multiple institutions, certifying over an optimal cohort of research professionals.
HRIG develops quality assurance frameworks and provides continuous monitoring to maintain compliance with international standards.
Example: A multi-specialty hospital will be able to implement HRIG’s QA system, aiming to reduce audit findings.
We offer project management, HR planning, accounting and bookkeeping, tax compliance and monitoring services for smooth research operations.
HRIG shall support establishment and maintenance of integrated systems including subject databases and centralized recruitment platforms for real-time trial tracking.
We translate consent forms and study materials into Filipino and regional dialects to ensure better participant understanding and ethical compliance. We also provide translated materials to support research dissemination.
HRIG assists in research dissemination from manuscript development to journal submission.
Example: A suitable research management training program shall be offered, with support provided throughout the full research management cycle.
Pharmacovigilance is a critical component in ensuring participant safety and regulatory compliance. HRIG provides plug-and-play systems for safety monitoring, recruitment oversight and facility procedures for adverse event reporting.
Example: In a Phase III oncology trial, HRIG will support detection of early safety signals through pharmacovigilance, leading to protocol adjustments and minimized participant risk.
HRIG advocates for streamlined ethics review and policy reforms while building networks for harmonized digital and regulatory processes. It will support networking activities among similar groups.
Our service offerings are designed with modularity and scalability in mind, allowing us to configure and customize each solution to align with the specific operational requirements and objectives of our clients and partners.