Orphan Drug Consulting offers end-to-end management support to pharmaceutical and biopharmaceutical companies launching in the EU, US and across the world. From strategic advice and corporate development through supply chain, quality assurance, compliance, vendor management to product launch, we are here for you. 

The Orphan Drug Consulting team bring over 150 years of combined experience in supply chain and quality assurance to support your organisation in bringing your products from clinical to commercial launch.

By utilizing specific allowances and reimbursement programs open to Orphan Drugs in different countries to optimise supply, your product can be on the market quickly with production runs and SKU’s for small patient populations kept to a minimum.

Understanding and aligning your supply across the differing legal, tax, customs, finance, regulatory and compliance framework to ensure successful supply can be challenging, especially when your product is utilizing routes to market such as early access programs or named patient supply. Orphan Drug Consulting is here to navigate these legislative frameworks on your behalf and ensure that your patients receive seamless product first time and every time across the world.