For Pharma & Sponsors

For Pharma & Sponsors.

Are you a pharma company looking for support in efficiently coordinating your clinical trials? VALEA delivers comprehensive solutions — from logistics consulting to selecting and placing experienced study nurses to optimising recruitment and retention.

Why VALEA

Smooth trial workflows and optimised inclusion numbers — through study end.

We know the formal requirements as well as the temporal and spatial hurdles that make clinical trial delivery increasingly demanding. Our ambition: to optimise your trial output.

That is why we have been asking the decisive questions for years — and developing targeted solutions.

After the medical informed-consent discussion, study nurses support participants' understanding of trial processes, take up open questions and route medical or trial-specific queries back to the site. Home visits reduce additional burden and make participation easier to fit into everyday life — patient-centred, structured and in line with the site's responsibilities.
VALEA Clinical supports trial sites with clear pre-screening workflows, coordinated trial processes and traceable documentation paths. Medical eligibility and patient outreach remain the responsibility of the site and the responsible investigators.
Trial visits are prepared and coordinated so that workflows remain plannable for the site, the study nurse and participants. Aligned time windows, defined responsibilities and forward-looking communication ensure trial processes are delivered reliably, protocol-compliant and with minimal burden.
Retention grows where trial participation remains compatible with everyday life. VALEA Clinical supports this through consistent contact persons, personal care in the home environment and plannable processes. This reduces practical hurdles and supports long-term participation.
Visit data is documented in a structured, timely and traceable manner. Internal QC checks support completeness, plausibility and data quality — following clear documentation workflows and in line with the study protocol, site requirements and QMS standards.
Monitoring findings and queries show where processes can be sharpened. VALEA Clinical analyses anomalies in a structured way, derives improvements and thereby strengthens quality, traceability and trial performance in ongoing operations.
Sample service package

Tailored. Complete. Reliable.

VALEA Clinical develops a tailored service package for every trial project — based on the study protocol, site requirements and operational risk. The focus is quality-assured delivery in real-world trial operations: clear workflows, qualified study nurses, structured communication, traceable documentation and QC review according to internal QMS standards.

The result is Home Trial Support that is not just organised — but delivered in an auditable, traceable and quality-assured way.

Special service

Site Nurse Service — SNS

Operational trial support by qualified study nurses and study coordinators — for trial sites, sponsors and CROs.

VALEA Clinical works in a structured, GCP-oriented way and according to an ISO-based quality management system.

More about SNS →
Special service

Home Trial Support — HTS

Trial-related home visits by qualified study nurses — according to protocol, site requirements and clear quality standards.

VALEA Clinical combines patient-centred delivery with structured visit documentation and QC-oriented quality assurance.

More about HTS →

Too much information?

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