Expert guidance in building and scaling high-performing Quality and Supply Chain organizations
Schedule a ConsultationThe consulting team at Black Diamond Biopharmaceuticals each have over 20 years of experience, knowledge, and leadership in the biopharmaceutical industry. We deliver expert guidance in building and scaling high-performing Quality and Supply Chain organizations.
Our experience covers the full spectrum of clinical trials management from Phase I start-up to Phase IV, expanded access programs (EAP), and investigator sponsored trials (IST). We specialize in end-to-end solutions that ensure compliance, efficiency, and patient-focused delivery.
End-to-end setup and execution of clinical trial supply chains — from study start-up to closeout. We manage forecasting, production, and distribution to meet First Patient In (FPI) targets across all phases.
Prepare your organization for successful FDA, EMA, PMDA, and MHRA inspections with our proven PAI Toolkits, training, and mock interviews.
Build robust end-to-end clinical supply chains, forecasting, vendor management, procedures, and production strategies — saving time, reducing risk, and cutting costs.
From sourcing to contract negotiation and oversight, we help improve supplier performance and reduce cost and lead times.
Create scalable, collaborative teams with our mentorship programs, Centers of Excellence, and training strategy — reducing onboarding time by 50% and improving staff retention.
End-to-end experience with drug delivery systems and container closures—from injectables (auto-injectors, PFS, IT, IV, SC, IM) to oral forms—covering small molecules, biologics, and RNAi.
"Black Diamond Biopharmaceuticals was instrumental in preparing our team for regulatory inspections. We passed with zero observations."
"Their clinical supply chain insights saved us millions — and more importantly, ensured no missed doses."