External Manufacturing Support
At Pre-therapeutic, we offer tailored support in managing CMOs, CDMOs, and other key vendors involved in your drug development programme. From sourcing GMP materials to overseeing outsourced manufacturing, we ensure that your partners meet the technical, regulatory, and quality standards required for successful early-phase development.
Our Services Include
Vendor Identification & Qualification
We help select and qualify the right partners for your needs—evaluating technical capability, regulatory history, and timelines.
Vendor Audits & Oversight
We conduct audits and provide ongoing CMO/CDMO oversight, including batch review, deviation handling, and regulatory data coordination.
GMP Material Management
We assist in sourcing and qualifying GMP materials, ensuring supply chain integrity from the start.
Why It Matters
Early-stage programmes often rely on a network of specialised providers. Our team ensures your vendors are aligned with your project goals, quality expectations, and regulatory strategy—reducing delays, avoiding compliance risks, and supporting a smooth path to clinic.