No two clinical trials are alike. Our highly experience project managers ensure your clinical supply chain is tailored to the needs of your protocol, clinical sites and patients.

KLIFO’s expert sourcing team works with our global supplier network to develop sourcing strategies that are right for your trial. We evaluate supply based on availability, price, lot size, expiry date, risk, security (FMD/DSCSA compliance) and intended country of use.

Including single panel labels and booklet labels. Our service spans from initial compliant text creation, through translation and regulatory review, to printing and inspection of finished labels.

From masking of active and placebo/comparator products for use in double-blind trials, through to ensuring blindness is maintained throughout our operational processes, KLIFO has extensive experience.

Of IMPs, comparators, and ancillaries for double-blind and open-label studies. Our packaging facilities include purpose-built packaging suites for temperature- (controlled room temperature, refrigerated and frozen products) and light-sensitive products.

At -80°C, -20°C, 2-8°C, and 15-25°C, ensuring product integrity. KLIFO’s facility offers significant capacity across all temperature ranges to support even the largest and most complex clinical trials.

KLIFO’s expert team will advise on the best distribution strategy for your trial – whether through direct site shipments from KLIFO, or through our network of approved depots. Each year KLIFO executes thousands of shipment to clinics across the world.

QP consultancy, auditing and release services available as standalone services or as part of a broader CTS project. Our extensive team of dedicated QPs ensures resource constraints do not become a bottleneck in the CTS process.

KLIFO, and our approved depot partners, offers accountability to shipper, kit and unit dose level. Certified destruction of unused and returned medications is performed promptly upon client approval.