Clinical supply,
simplified.
Comparator sourcing, GMP packaging and labelling, QP release and temperature controlled delivery — coordinated end to end from Switzerland and the Netherlands.
- Presence in Switzerland and the Netherlands
- GDP certified and GMP aligned across every service
- Swissmedic and EMA regulatory alignment
- Member of the Swiss Biotech Association
Built for agility. Driven by purpose. Trusted for quality.
Cure Pharma was founded to bring simplicity, reliability and speed to clinical supply. We saw fragmented supply models holding studies back and built a connected alternative, backed by regulatory expertise and global execution.
Our story
Our founding team came from inside the industry with hands-on experience in managing pharmaceutical supply chains: managing global supply chains, sourcing rare comparators, navigating regulatory complexity. We knew the pain points first-hand — rigid vendors, unclear accountability and delays that cost time and money. Cure Pharma exists to remove them.
Our team
Leadership and operations combine pharmaceutical, clinical supply, regulatory and logistics experience. A flat structure and lean processes mean quick decisions, consistent communication and personal accountability. We are hands-on, reachable and we deliver what we promise.
- Leadership
Industry veterans with deep pharmaceutical and supply chain expertise.
- Quality
Specialists in regulatory compliance and quality assurance.
- Operations
Experts in global logistics and clinical supply coordination.
Our solutions
Tailored support at every stage of the clinical supply chain.
Clinical supply management
One team from sourcing to QP release.
We manage sourcing, transport, storage and release as one integrated process, with a single point of contact who owns the schedule. Whether you want us to manage your clinical supplies or only require selected services, our team is here to help.
- One contact accountable for every vendor and milestone
- Proactive risk and exception management
- A setup that flexes from modular to full service
Comparator sourcing
Originators, generics and biosimilars, found and documented.
Our global network reaches the markets where your comparator actually sits, including hard-to-find products. Every supply arrives with the paperwork your QA team will ask for.
- Batch-specific sourcing with full traceability
- Complete documentation, including CoA and CoC
- Feedback on availability within 24 hours
Packaging & labelling
Kits that match the protocol and the country.
From relabelling market packs to building custom clinical kits with multilingual booklet labels. Primary and secondary packaging, blinding and randomisation, all under GMP.
- GMP primary and secondary packaging
- Country-compliant multilingual labels
- Blinded randomisation
QP release & regulatory
Release without delay. Compliance without doubt.
EU QP release coordinated against your study timeline, with audit-ready documentation from the first shipment. We work only with qualified partners and keep the file complete as the study changes.
- QP release scheduled around first-patient-in
- Swissmedic and EU alignment across markets
- Audit-ready files kept current, not reconstructed
Logistics & depot management
Frozen, cold and ambient — tracked to the last mile.
Validated temperature-controlled shipping, depot storage close to your sites, and full reverse logistics. We collect and destroy unused or expired products with documentation you need.
- Handling at −80 °C, −20 °C, 2–8 °C and 15–25 °C
- Inventory visibility by location, batch and expiry
- Returns and destruction, fully documented
Global Access Programs
Expanding access to life-saving therapies worldwide through Named Patient Programs (NPP), Post-Trial Programs, and urgent hospital supplies.
We bridge critical access gaps by facilitating ethical, compliant pathways for named patient-treatments, Post-Trial Programs, unregistered innovative therapies, and essential medicines facing critical market shortages.
Whether managing global Named Patient Programs (NPP), Post-Trial Programs or sourcing emergency unlicensed supplies for hospitals and clinics, we ensure full regulatory compliance, complete traceability, and validated temperature controlled deliveries.
- Fully compliant Named Patient Program (NPP) & Post-Trial Managed Access execution
- Global sourcing for unlicensed, hard-to-find, and shortage medicines
- Rapid, GDP-compliant global sourcing of critical commercial medicines, ensuring continuous patient care in hospital and clinical settings.
- Validated, temperature-controlled last-mile delivery directly to hospitals.
Regulatory toolBETA
AI Clinical Supply Regulatory Advisory
Do not gamble with your trial execution. Understand beforehand your comparators and IMP regulatory needs, mitigating bureaucracy delays and protecting your trial timelines. We help you understand in advance the regulatory framework behind your clinical projects, with an AI-powered tool built by Cure Pharma.
- The governing health authority for any origin–destination route
- What the destination country requires for import
- Free to use, for preliminary planning; verify with your QP or local partner
More than 80% of trials face sourcing delays. Ours don't.
Cure Pharma — comparator sourcing
Our process. Your peace of mind.
Every project starts with understanding the trial, not the shipment. We map your supply needs across availability, sourcing, storage, transport, QP release and packaging — then adapt as the study moves.
Partnership first
Transparent timelines, solutions scaled to trial size and complexity, and a modular setup that steps in exactly where you need it.
One point of contact
Vendor coordination, shipment and release scheduling, status reporting, escalations and change requests — handled by one named person.
Quality and compliance
GDP and GMP standards across services, a qualified vendor network, and traceable, audit-ready documentation by design.
Supply chain visibility
Shipment and release status, inventory by location, batch and expiry, plus escalation alerts before you have to ask.
Held to the degree
Frozen, refrigerated and ambient product handled in validated conditions, with a documented temperature record from depot to site.
Frozen−80 °C and −20 °C
Biologics and investigational product requiring deep freeze.
Refrigerated2–8 °C
The standard cold chain for most comparator and reference products.
Controlled ambient15–25 °C
Room-temperature product kept inside its validated range, not just indoors.
Work where decisions are quick
We are small, flat and hands-on. If you have worked in clinical supply, QA or logistics and want fewer layers between you and the work, we would like to hear from you.
- Clinical Supply Project ManagerRotkreuz, CH | Remote, EU
- Senior Business Development, Clinical SupplyRemote, EU
- Supply Chain ManagerRotkreuz, CH | Remote, EU
- Sourcing Associate, comparatorsRemote, EU
No matching role open? Send an open application. We read everything and answer within two weeks.
Let's simplify your clinical supply chain
Tell us about the study phase, countries, timelines and we will come back with a concrete plan, not a brochure.
Suurstoffi 12b
6343 Rotkreuz
Posthoornstraat 11
3011WD Rotterdam