Terms and operating notice

Last updated: 27 August 2026. This website provides general information about professional medicine-access, regulatory-affairs and coordination services offered by RIVERPHARMA LTD.

Professional information only

The site is intended for healthcare organisations, medicine developers, manufacturers, marketing authorisation holders, clinical-trial sponsors, CROs, research sites and other professional organisations. It is not intended for patients or consumers. Website information does not replace formal medical, clinical, legal, scientific or regulatory advice for a specific product or procedure.

No supply or availability offer

Website content, a response to an enquiry or an introduction does not constitute an offer to sell or supply a medicinal product, confirm availability, reserve stock or guarantee that any access pathway is lawful or achievable.

Riverpharma’s operating boundary

Riverpharma provides access-pathway research, regulatory-affairs project support and non-transactional coordination services. It is not a pharmacy, prescriber, manufacturer, regulator, marketing authorisation holder or wholesale dealer. Riverpharma does not itself buy, sell, stock, dispense, import, export, transport or physically handle medicinal products and does not hold a WDA(H).

Any regulated procurement, importation, storage, distribution or supply is undertaken directly by separately contracted, appropriately authorised organisations, subject to their own assessment, applicable law and required approvals.

Regulatory affairs support

Regulatory affairs work may include pathway and legal-basis mapping, dossier-readiness coordination, submission planning, product-information workstreams, authority-question tracking and post-authorisation lifecycle coordination. The exact scope is agreed for each professional engagement.

Riverpharma does not act as a regulatory authority, applicant, marketing authorisation holder or legal representative. The applicant or marketing authorisation holder remains responsible for the dossier, declarations, formal submissions, fees, statutory obligations and product lifecycle. Regulatory acceptance, authorisation, timing or outcome is never guaranteed.

Specialist logistics coordination

Where agreed as a secondary service, logistics coordination is limited to administrative and project coordination between professional organisations. It may include requirements capture, documentation handovers, stakeholder communication, milestone tracking and exception escalation.

Riverpharma does not act as carrier, importer, exporter, warehouse or freight forwarder. It does not procure medicines, negotiate or conclude their sale or purchase, or act as a medicines broker. Each separately appointed organisation remains responsible for its licences, GDP duties, quality decisions, packaging, route, customs or import requirements and execution.

Responsibilities of professional users

You remain responsible for the accuracy and lawfulness of information supplied, your own professional and regulatory duties, clinical and prescribing decisions, due diligence, approvals, licences, import requirements and the terms of any engagement with a third party.