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© 2026 cohaga AG · All Rights Reserved · St. Gallen, Switzerland · Imprint745,629 companies indexed · Last updated: today
DirectoryBusiness & Technical ServicesResearch & DevelopmentArzoCross Research SA
Cross Research SA Logo
Verified· 2 sourcesTrust Score
Summary

About the company

The core activity of CROSS Research SA is the conduct of clinical trials, particularly Phase I trials, for the pharmaceutical industry. The company offers services such as central clinical laboratories, analytical laboratories for drug analysis and pharmaceutical laboratories for the development of drugs. It also conducts safety studies, dose-finding studies, bioavailability and bioequivalence studies, as well as specialized studies such as skin adhesion studies and medical device testing.

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Products & services

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Cross Research SA

✓ Offered9
Phase I studies in healthy volunteers
Phase I studies in healthy volunteers and special populations to assess safety, kinetics, disposition, exposure profile and appropriate dosing; including SAD, MAD, local tolerability and DDI studies.
Clinical development consulting and project development
Overall evaluation of clinical development plans, support for Scientific Advice, assessment of Phase I to Phase II/III projects, and budget planning for clinical programs.
Study planning and protocol authoring
Tailored protocol synopsis and complete ICH-compliant study protocols in collaboration with biometrics, clinical project leaders, investigators and biostatisticians.
Identification and selection of clinical trial sites
Selection, qualification and auditing of clinical sites, building site databases and access to clinical networks in Switzerland and other European countries.
Coordination of international clinical trials
Coordination of Phase I/II/III studies in Europe with a single central point of contact; involvement of authorities, ethics committees, laboratories, monitors and local CROs.
Biometrics and PK services
Study protocol and CRF design, sample size planning, statistical reports and TFLs; pharmacokinetic analyses with validated systems and databases.
Medical Writing
Creation and revision of Clinical Study Protocols, Clinical Study Reports, Investigator’s Brochures, IMPD and other regulatory documents and abstracts.
Quality Assurance, Audits and GCP trainings
SOP-based quality assurance, documented checks, subcontractor audits, facility and trial audits, and GCP trainings for investigators and study staff.
Regulatory support for clinical studies
Preparation and submission of CTA packages to ethics committees and authorities, as well as support with authorities’ questions during the approval process.
Trust & reputation

ranQ Trust Score of Cross Research SA: 4.1 out of 5.0

Trust Score4.1/ 5.0

High

x

Data basis 54% · As of October 2026

Without public customer reviews the score stays capped.

Cross Research SA has no value in the Reputation area of the ranQ Trust Score because no data is available. The area carries 42% of the weighting and drops out of the calculation for this profile; it does not lower the score, only the reported data basis.
x
CriterionValueWeight
  • Review quality: No data point — the criterion is taken out of the weighting and does not lower the score.—24%
  • Review volume: No data point — the criterion is taken out of the weighting and does not lower the score.—10%
  • Review recency: No data point — the criterion is taken out of the weighting and does not lower the score.—8%
Cross Research SA scores 89.3 out of 100 points in the Substance area of the ranQ Trust Score. This area carries 28% of the weighting.
x
CriterionValueWeight
  • Establishment: Years since founding or brand launch, logarithmic. The maximum is reached at 15 years.100.012%
  • Company size: The headcount band, researched by ranQ or stated by the company. It is scored in steps rather than by head count, because the data only provides bands.70.07%
Cross Research SA scores 83.3 out of 100 points in the Identity area of the ranQ Trust Score. This area carries 22% of the weighting.
x
CriterionValueWeight
  • Verification: Official register entry (commercial register with UID or professional-body record, 55 points), confirmed domain (20 points) and confirmed ranQ profile (up to 25 points, depending on completeness).83.322%
Cross Research SA scores 28.6 out of 100 points in the Visibility area of the ranQ Trust Score. This area carries 8% of the weighting.
x
CriterionValueWeight
  • Website authority: Ahrefs' Domain Rating measures, on a scale of 0 to 100, how strongly a website is linked from other websites. For Swiss SMEs the range up to 40 is typical; the maximum is reached at 35.28.64%
  • Media authority: No data point — the criterion is taken out of the weighting and does not lower the score.—4%
Qualifications+0.00

Cross Research SA reaches a ranQ Trust Score of 4.1 out of 5.0 — rated «High». No public customer reviews are available for this provider; the rating is based on the remaining criteria. The data basis is 54%, so the score is backed by part of the criteria. As of October 2026.

The Trust Score cannot be bought and is calculated from publicly verifiable data.

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Location

Via Francesco Antonio Giorgioli
6864 Arzo

At a glance

Legal form
Corporation
UID
CHE-108.671.859
Founded
1997 · 29 years
Last commercial register change
March 3, 2021
Employees
11 to 20
Legal form: Graded by liability and disclosure. The weight is kept small: a sole proprietorship is not a dubious company, it is just liable differently.
100.0
6%
  • Branch offices: Branch offices linked in the commercial register. Having none is normal and costs no points.70.03%
    • Full methodology

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