For CROs and trial sponsors
Comparators, reference listed drugs and ancillary medicines, with single-batch supply where available, long shelf life and full pedigree documents.
In short
Contract research organisations and trial sponsors use MedsAcross to source comparators, reference listed drugs and ancillary medicines for clinical trials. We verify the company and the protocol reference, propose lots with batch and expiry, reserve them on acceptance and ship to depots or sites with chain-of-custody documents.
What we supply
- Comparators, innovator and generic
- Reference listed drugs for bioequivalence studies
- Ancillary, premedication and rescue medicines
- Shipments to several depots and sites
How we verify you
Verification happens once per organisation and is renewed when a document expires.
- Company registration and tax ID
- A protocol or study reference
- Depot or site licences where the destination requires them
Prices
Quote only, per lot, with validity and lead time.
Legal routes
Rules differ by country and change over time. Each note cites a regulator or a published legal analysis. Your local regulatory adviser confirms the route for your case.
Comparator buyers expect a certificate of analysis, stability data and full comparator documentation.
Source: Pharmaceutical Technology, comparator sourcing case study
Indian manufacturer export NOCs are issued in 7 working days and stay valid for one year under the NOC 2.0 process.
Source: Lexplosion, CDSCO export NOC 2.0
Services for you
- Clinical trial comparatorsComparators, reference listed drugs and ancillaries with batch, expiry and pedigree documents for every lot.
- Cold chain logistics2 to 8 °C and frozen lanes with qualified shippers, data loggers and good distribution practice.
- Regulatory documentsCertificates of analysis, COPP, GMP certificates and export paperwork, organised for your regulator.
Questions and answers
Do you supply reference listed drugs for bioequivalence studies?
Yes, where the reference product is available from the market your regulator specifies. We document the source market, batch and expiry for your dossier.
Can we see the certificate of analysis before ordering?
We share the certificate of analysis for the proposed batch before you accept, where the source allows it.
Do you work with our clinical supply partner?
Yes. We can ship to your packaging partner or depot and send the documents to both of you.
Other buyers we serve
Request comparator availability
Send the product list, quantities, minimum shelf life and destination depots.