One accountable chain, end to end
Everything we do covers one route: the journey a medicine takes from a production line to the institution or patient waiting for it, and the documentation that journey requires at every stage.
Wholesale distribution
Branded and generic medicines, nutraceuticals and surgicals to hospitals, institutions and distributors.
02Contract manufacturing
Production on lines already built, validated and inspected — under your brand, to your specification.
03Named patient supply
Sourcing, permits, cold chain and delivery for a single identified patient, through their physician.
04Reference listed drugs
Innovator reference and comparator products from the market of origin your filing requires.
05Exports and international supply
Registration, labelling, permits and shelf-life on arrival resolved before a consignment ships.
06Cold chain and supply chain
Validated packing, data logger monitoring and an excursion protocol agreed in advance.
07Registration assistance
CTD and ACTD dossiers, CPP, free-sale certificates, legalisation and apostille for your authority.
08Tender and programme supply
Documentation, pre-qualification support and pricing for hospital, government and NGO procurement.
09Medical information
Stability data, handling requirements and market differences from manufacturer documentation.
Wholesale distribution
We supply branded and generic medicines, nutraceuticals and surgicals to hospitals, pharmacies, healthcare institutions and distribution partners, managing every step from sourcing through to delivery.
Authenticity is the point of the exercise. Product is bought from verified manufacturers and licensed suppliers, moves under GDP-compliant conditions, and arrives with the documentation to prove where it has been.
- Purchased only from authorised manufacturers and licensed wholesalers
- Branded medicines, generics, nutraceuticals and surgicals
- Hospital and institutional accounts
- Temperature-controlled handling where the product requires it
- Analysis certificates travel with each consignment
- Batch, source and custody documented per unit
- Serves
- Hospitals, institutions
- Categories
- Pharma, nutra, surgicals
- Cold chain
- Available
- Standards
- GDP
Contract manufacturing
Building and validating a pharmaceutical facility takes years and consumes capital that most products cannot justify. Contract manufacturing puts your product onto lines that are already built, already validated and already inspected — produced under your brand, to your specification.
We work to each client’s product requirements, timelines and target-market standards, so what comes off the line is ready for the market it was made for rather than needing rework before it can be filed.
- Formulation and development support
- Scale-up and technology transfer from an existing site
- Commercial production under GMP conditions
- Analytical testing, stability studies and batch release
- Packaging, artwork and destination-market labelling
- Regulatory documentation to support your filings
- Dosage forms
- [list forms]
- Batch sizes
- Flexible
- Standards
- GMP
- Output
- Full batch records
Named patient supply
A named patient programme allows one specific, identified patient to receive a medicine that is not registered or not marketed in their country, on the prescription of their treating physician. Most regulatory systems provide for this, because approval timelines do not move at the speed of an individual illness.
We manage the case end to end: identifying an approved source, confirming the route available in that country, assembling the file the importing authority requires, shipping under the right conditions, and setting up resupply before the next consignment becomes an emergency.
- Feasibility and honest timeline before you commit
- Sourcing from licensed suppliers at origin
- Import permit application and regulatory file
- Prescription, justification and physician declarations
- Cold-chain shipping and destination customs clearance
- Scheduled resupply for continuing treatment
- Typical timeline
- 1–4 weeks
- Starts with
- A valid prescription
- Minimum order
- One patient course
- Route
- Destination country law
Please read. Every named patient import begins with a valid prescription from the treating physician and follows the import law of the destination country. We cannot supply without one, and we cannot advise whether a treatment is appropriate for a particular patient — that judgement belongs to the prescribing doctor.
Reference listed drugs
A bioequivalence study is only as defensible as the reference product it was run against. Obtaining that product — correct strength, correct market of origin, sufficient remaining shelf life, documentation that survives regulatory review — is routinely the slowest step in a generic development programme.
It becomes considerably harder when the reference is discontinued, supply-restricted, sold only through hospital channels, or marketed in a single country where you have no presence. That is the category we work in.
- FDA and EMA approved reference products
- Sourced from the market of origin your filing requires
- Comparator supply for clinical trial programmes
- Restricted-distribution and limited-supply products
- Batch and expiry confirmed before purchase
- Full purchase documentation and chain of custody
- Serves
- Generic makers, CROs
- Origin market
- As your filing requires
- Shelf life
- Matched to study window
- You provide
- Registration, purpose
Exports and international supply
Pharmaceutical export failures are almost never freight failures. They are documentation failures discovered at a border, with product sitting in a bonded warehouse while its shelf life runs down.
Every destination market sets its own requirements: registration status, import licensing, labelling language and content, minimum remaining shelf life on arrival, and which certificates the importing authority will accept. We resolve those before a consignment is committed.
- Market-specific regulatory documentation
- Certificates of analysis, free sale and GMP certificates
- Labelling and artwork compliant with the destination
- Export clearance with the importer of record
- Temperature-controlled freight on qualified lanes
- Commercial invoice, packing list and certificate of origin
- Markets
- [list confirmed markets]
- Documentation
- Prepared before shipping
- Freight
- Ambient and cold chain
- Clearance
- Destination partners
Cold chain and supply chain
A biologic that spends four hours outside its temperature range is no longer the product that left the manufacturer, whatever the carton says. For oncology agents, biologics and antivirals, cold chain is not a service feature — it is the condition on which the product remains usable at all.
Our network keeps every shipment traceable, temperature-controlled and compliant with import and export regulation, with the excursion protocol agreed in advance rather than improvised on arrival.
- Collection from the licensed supplier under travelling conditions
- Validated packing matched to route duration and ambient conditions
- Data logger monitoring across the whole journey
- Shipment status visible to you throughout
- Defined excursion, quarantine and disposition procedure
- Temperature record handed over on delivery
- Typical delivery
- 3–4 weeks
- Monitoring
- Data logger
- Collection
- At origin
- Record
- Supplied on delivery
Registration assistance
Getting a product registered in a new market is usually slower than getting it made. Each authority specifies its own dossier format, its own certificate requirements and its own legalisation chain, and a submission that misses any of them goes back to the start of the queue.
We prepare dossiers and supporting documents to your regulatory authority’s format, and coordinate the certificates and legalisation that sit around them.
- Dossiers in CTD and ACTD format
- Certificate of Pharmaceutical Product (CPP)
- Free-sale certificates and GMP certificates
- Legalisation and apostille
- Product literature and technical documents
- Guidance on the authority’s specific requirements
- Formats
- CTD, ACTD
- Certificates
- CPP, FSC, GMP
- Legalisation
- Apostille supported
- Output
- Submission-ready file
Tender and programme supply
Public-health procurement runs on tenders, and tenders are won or lost on paperwork before price is ever compared. A bid that arrives without the right certificates, in the wrong format, or with a product whose registration status is unclear is disqualified regardless of what it costs.
We prepare tender-ready documentation and pre-qualification material for hospital, government and NGO bids, with particular depth in oncology and HIV — the two areas where programme procurement is most active.
- Tender documentation prepared to the buyer’s format
- Pre-qualification support for institutional bids
- Registration status confirmed before you commit
- Programme supply for oncology and HIV
- Flexible quantities, from single lots to scheduled programme supply
- Supply continuity planned across the contract period
- Serves
- Hospitals, government, NGOs
- Focus
- Oncology, HIV
- Quantities
- Flexible
- Documents
- Prepared to format
Medical information
Institutional clients and clinicians frequently need product information that goes beyond a pack insert: stability data, handling requirements, storage conditions, presentation differences between markets, or the availability of alternative strengths.
We provide that from manufacturer documentation and published evidence, and we are explicit about the boundary. We supply product and regulatory information, not clinical recommendations.
- Stability and storage data from manufacturer documentation
- Handling and reconstitution requirements
- Presentation and strength differences between markets
- Availability of alternative strengths or formats
- Regulatory status of a product in a given market
- Documentation support for institutional review
- Serves
- Clinicians, institutions
- Sources
- Manufacturer evidence
- Response
- One working day
- Excludes
- Clinical recommendations
From first enquiry to delivered goods
Enquiry and quote
Send the product, strength, quantity and destination. We reply with availability, landed pricing and the documents your market needs.
Confirm and document
Specification agreed, registration and export paperwork prepared, supply plan confirmed before anything ships.
Source and verify
Product from licensed sources only, with certificate of analysis, batch records and packaging checked before dispatch.
Ship and hand over
Freight booked, cold chain held, documents travelling with the goods, and the temperature record handed over at delivery.
Licences and audit documents are available to qualified buyers. Drug licence, quality certificates and supplier documentation during qualification — ask for them with your enquiry.
End-to-end support, from first enquiry to after delivery
One team handles sourcing, documentation, shipping and follow-up, so you are not coordinating four suppliers who each hold one piece of the process.