Our GCP accredited pharmacists understand the needs of the study sponsor(s) and/or site and can customize processes to meet the study's requirements.

We work closely with the study sponsors, study investigators, site personnel and CRAs throughout the study process (from before commencement of the study until close-out).

This ensures a smooth and on-time running of the trial, including ensuring all deliveries of IPs are on time and within the specifications (documentation and temperature) required.

CompoundLabs has stringent processes and comprehensive documentation in its day-to-day operations, with enhanced procedures for clinical trials. We have built in additional processes beyond the minimum requirements to facilitate the smooth and straightforward monitoring by CRAs.

We can help with a range of services for your study that include (but are not limited to) the following:

• Procurement (including IP, capsules, fillers, packaging etc.)
• Preparation of IP and matching placebo products (non-sterile capsules, creams, powders, liquids, and troches/lozenges)
• Preparation of 'disguised' commercially available tablet/capsule and a matching placebo capsule
• Randomization plan and emergency break envelopes
• Storage at ambient, refrigerated (4°C to 8°C) or freezer (-25°C to 0°C) conditions
• Controlled drugs storage at ambient and refrigerated conditions
• Labelling (blinded/unblinded) as per protocol/Medsafe requirements
• Dispensing (individual participant dispensing is required under current legislation)
• Return, accountability and destruction (including controlled drugs) of any unused products
• Storage of all records for 10 years (or longer if required by the sponsor/site)
• Nationwide delivery under controlled temperatures with traceability
• Local hand delivery/pick up options available

At CompoundLabs, we understand the timing of dosing is crucial in clinical research. Therefore, we prioritise the compounding, dispensing and delivery of the medicines to sites, ensuring that dosing schedules are met.