Product & quantity
Specify the comparator, strength, dosage form, pack size and quantity, together with any preferred market presentation.
Clinical Trial Supplies
We source comparator medicines for clinical trials through our European and international supplier network, with your product specifications, batch requirements and study timelines in focus.

Sourcing for your study
Our sourcing starts with a clear understanding of the medicines your study requires. Together, we clarify the specifications and review suitable supply options.
Specify the comparator, strength, dosage form, pack size and quantity, together with any preferred market presentation.
Tell us whether you need a single batch or a limited number of batches. We review the available sourcing options against your requirements.
Share the required remaining shelf life and delivery schedule. Batch and expiry information is clarified as part of the supply discussion.
Product availability, batch quantities and expiry requirements are assessed for each enquiry before an order is agreed.
From specification to delivery
We bring sourcing, documentation and delivery requirements together so that the next steps can be agreed clearly.
Send the product details, quantity and destination. Add batch requirements, minimum shelf life and the required delivery date.
We approach suitable sources within our network and review product, batch and expiry details against your specification.
Availability, supporting documentation, commercial terms and delivery arrangements are agreed with you before the order.
Delivery is organised according to the agreed terms and the product’s requirements.
Logistics
Together with a specialised logistics partner, we offer worldwide transport and shipping logistics for medicines, with a particular focus on cold chain and temperature-controlled transport.
We organise temperature-controlled transport aligned with your medicines’ requirements, including cold-chain shipments.
We handle customs declarations for your international shipments and coordinate the required documentation with you.
From shipping arrangements to international delivery, we coordinate transport routes and schedules to match your requirements.
Documentation for your supply
Tell us which documents are required for your project. We clarify their availability for the selected product and source.
QualityProduct-related certificates of analysis (CoA), according to the agreed documentation requirements.
Origin documentation, including a certificate of origin (CoO) where required and available.
Batch release documentation and supporting batch and expiry information, as agreed for your supply.
Before your enquiry
Yes. Tell ADVIPHA whether your study requires a specific batch, a single batch or a limited number of batches, together with quantities, minimum remaining shelf life and delivery dates. Available sourcing options are assessed against these requirements before an order is agreed.
Please specify the required Certificate of Analysis (CoA) and Batch Release Certificate in your enquiry. ADVIPHA clarifies document availability for the selected product, source and batches and agrees the documentation requirements with you before the order.
Let’s discuss your study supply
Describe the medicines you need and add your study-specific requirements. Review the email draft before sending it to our team.
Review the text, then open your email application and send the enquiry there.