Simplify your supply
One supply model from development to commercial. Fewer handoffs between functions and partners, and one accountable owner for the whole chain.
Service area
End-to-end bespoke solutions that de-risk and accelerate our partners' and sponsors' drug and device development programmes.

Perspective
We model the enterprise as a connected value chain: the relationships, constraints and dependencies that drive performance across functions.
Traditional supply chain models reduce reality to a sequence of isolated steps, and miss how each decision moves every other.
We model the enterprise as a connected value chain: the relationships, constraints and dependencies that drive performance across functions.
We bring cross-functional trade-offs into one strategic decision framework and expose the value that stays hidden when each function optimises alone.
Technology and expertise
Clinical and commercial programmes demand a supply chain built for the product, the phase, the markets and the patients it serves. Our senior operators design it with precision, equip it with the newest tools in the field and drive its execution with your team.
One supply model from development to commercial. Fewer handoffs between functions and partners, and one accountable owner for the whole chain.
Risk-based safety stock and dual sourcing, sized so a single supplier failure does not interrupt dosing.Cold chain control and a decisive excursion response. Strategic oversight of every supplier your programme depends on.
Accelerating from first-in-human to launch and beyond: new product introduction, market rollout and life cycle management, executed to plan.
Precision
S&OP ownership and demand planning on SAP and Anaplan. Patient-level modelling: recruitment, dosing intervals, dropout. Risk-based safety stock. Scenario planning and CMO capacity alignment. Launch ramp and market rollout sequencing.
Investigational product protected at every step, from first-in-human to final reconciliation, planned so each enrolled patient can be dosed on schedule. IRT and IXRS set-up, management and decommissioning. Clinical packaging, labelling and booklet design. Cold chain and GDP distribution with excursion response. QP release, QPPV networks and import licences. Pharmacy manuals and site readiness. Structured trial close-out, from reconciliation to destruction.
CDMO and CRO scouting and sourcing. RFQ management from specification to award. Product tech transfer into the receiving site. Slot management, batch records and campaign oversight.
Strategic sourcing, contracting and delivery. Supplier performance, savings and compliance. Public tenders prepared and managed. Tariffs, import duties and customs clearance.
Inventory strategy, depot network and FIFO control. Dual sourcing, backup site qualification and safety stock sized to risk.
New market, new facility or new function, built from a blank page to a licensed, running capability. Licensing pathways with HPRA, MHRA, FDA and EMA. SOP development, quality systems and GMP readiness. ERP selection and implementation. CMO network design and backup site qualification. Serialisation and packaging line adoption.
Release and stability testing programmes. Contract laboratory management. Sample logistics and chain of custody. Analytical method transfer. Results expedited when a release date depends on them.
QP and QPPV coordination. Deviations, change control and licence variations handled with precision, without stalling supply.
Strategy
Strategic value chain design and a target operating model, then the transformation programme we drive to completion.
We pinpoint where value is made and lost across development, manufacturing and supply, then set the choices that follow: what stays in house, what goes to partners and where to invest.
The organisation, processes, systems and partners your supply chain needs for its next phase, defined as one model with clear decision rights.
Systems, data, roles and partners moved onto the target model. We drive the change with your team and execute it to plan.
NPI planning and launch readiness that accelerate the path to market, then the steady state and the life cycle changes that follow.
Engagement
A senior operator inside your team for a defined scope and period, executing in your systems and your meetings.
Senior capacity for a set number of days each month, for programmes that need a steady hand rather than a full-time hire.
A defined project with a charter, a plan and an end date, driven to completion by a Viaclin lead.
A precise answer when you need one: a question resolved, a document reviewed or a strategic decision supported, without a retainer.
First step
A thirty-minute call. We ask about the programme, the phase, the systems and the deadline. If we are the right team, a written proposal follows: scope, network specialists, timeline and fee. If we are not, we say so and point you to someone who is. A named lead, a plan with owners and dates, and delivery we answer for.
One-step connect: info@viaclin.com