Study Drug Management Services
Ensuring the integrity, safety, and regulatory compliance of investigational products is critical to the success of any clinical trial. At Global MedTrial LLP, we offer end-to-end study drug management solutions designed to support seamless drug handling, preparation, accountability, and disposal—tailored to meet the specific requirements of each study protocol.
Our Comprehensive Drug Management Capabilities Include:
We manage re-labeling and re-packaging activities at clinical sites, ensuring all investigational products are correctly labeled in accordance with study protocols and regulatory requirements.
Our trained professionals perform drug preparation under aseptic conditions for a variety of administration routes, including:
- Intravenous (IV)
- Subcutaneous (SC)
- Intraarticular
- Intraocular
- Intramuscular (IM)
This ensures product sterility and accuracy in dosage, minimizing risk to study participants.
We offer precise drug dilution services for oral, topical, and parenteral formulations, ensuring concentration accuracy and consistency as defined by the protocol and product specifications.
To maintain safety and compliance, we provide authorized local drug destruction services for expired, unused, or compromised study drugs, ensuring environmentally responsible and regulatory-compliant disposal.
Our team ensures full accountability and traceability of investigational products throughout the trial. Services include:
- Real-time inventory tracking
- Documentation of drug receipt, dispensing, and return
- Reconciliation and discrepancy resolution
- Audit-ready record maintenance
At Global MedTrial LLP, we prioritize efficiency, precision, and compliance in every facet of drug management. Our goal is to safeguard your study’s integrity while enabling timely and compliant delivery of investigational treatments to patients.
Partner with us for reliable, protocol-driven drug management solutions that meet global standards.
Looking to streamline your clinical research?
With our structured, high-touch approach to site oversight, Global MedTrial LLP ensures operational continuity, faster enrollment, and consistent quality—empowering sponsors and CROs to achieve clinical milestones with confidence.