Every development journey comes with critical decisions and hidden risks. At KLIFO, we help you anticipate them, align strategy with execution, and build programmes that regulators and investors can trust.

CMC gaps can delay approvals, increase costs and weaken investor confidence. KLIFO’s senior consultants step in to align science, manufacturing and regulatory compliance, taking ownership from strategy to execution.

Strong approvals are built decision by decision: what to generate, when to engage, how to document. KLIFO partners with you to anticipate risks, prepare clean dossiers and keep momentum.

Clinical development turns drug candidates into therapies by aligning science, indication, and regulatory demands. At KLIFO, we support biotech and pharma leaders in defining strategies, fostering cross-functional collaboration, and integrating all key elements.

When running a Clinical Trial Supply, every detail matters. And Clinical Trial Supply (CTS) are no exception. At KLIFO, we combine strategic insight with operational excellence to manage your clinical supply chain end-to-end — ensuring you deliver for your sites, your patients, and within your budget.

Every clinical programme faces safety risks, from trial design to post-marketing signals. KLIFO helps you anticipate them, design lean safety frameworks and act with regulatory confidence. That’s how we keep your drug’s journey safe at every stage.

KLIFO provides quality assurance solutions for pharma and biotech companies, combining strategic consulting with operational execution across all GxP areas.

Before any human trial, the quality of your non-clinical data determines whether you can move forward with confidence. KLIFO’s senior consultants help design and manage studies that regulators can trust and developers can build on.

KLIFO offers a managed Veeva Vault for EDMS and eTMF: secure, compliant, plug & play document management tailored for biotech, with no implementation project required.