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DirectoryBusiness & Technical ServicesResearch & DevelopmentNeuchâtelGALSER SA
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GALSER SA

Summary

About the company

The core activity of GALSER SA is the conduct of clinical trials for pharmaceutical and biotechnology companies as well as academic organizations. In this context, the company offers services such as project management, patient recruitment, risk-based monitoring, data management and regulatory affairs to efficiently and qualitatively conduct clinical trials.

AI-generated
Offering

Products & services

Industry:Research & Development
✓ Offered12
Project management for clinical studies
Project management for clinical studies, including control of timelines, budget and quality; KPI tracking, vendor coordination, flexible resource planning and structured communication with sponsors.
Regulatory affairs consulting services
Advisory services on Swiss regulatory processes, submissions, approvals and compliant study conduct; including support for Swissmedic and ethics committees.
Legal representation in Switzerland
Swiss legal representation and regulatory support for clinical studies, with compliant interactions with Swissmedic and ethics committees.
Study planning and protocol writing
Study conception, clinical development planning and creation of protocols; including scientific rationale, regulatory alignment and accompanying documents such as IB, ICF, SAP and Synopsis.
Study start-up
Study start-up activities for clinical studies, including feasibility assessments, site selection and preparation of key documents.
Site management
Management of clinical sites with initiation visits, investigator trainings, retrainings, ongoing communication, support and performance monitoring.
Clinical study data management
Database design and implementation, data validation, query management, secure data storage, archiving and preparation for statistical analyses.
Biostatistics
Statistical study planning, creation of SAPs, interim and final analyses, statistical reports, as well as support for submissions and publications.
Risk-based Monitoring
Monitoring of clinical studies using risk-based strategies, on-site and remote visits, data verification, QA and support for sites.
Study Close-out
Structured study close-out with database lock, final validation, budget reconciliation, archiving of essential documents and preparation of regulatory submissions.
Inspection and Audit Support
Preparation and support for audits and inspections, with assistance to ensure readiness and compliance.
Additional clinical support services
Strategic additional services beyond day-to-day study operations, including IMP logistics, vendor oversight, feasibility, registration, insurance, audits and publications.
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Reviews

Aggregated rating

Aggregated rating
4.5
of 5

Aggregated from 2 reviews across all connected sources

Sources
GGoogle4.52
★TrustpilotSoon
PProvenExpertSoon

Further sources are added continuously and factored into the ranQ Rating.

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Location

Rue des Beaux-Arts 8
2000 Neuchâtel

At a glance

Legal form
Corporation
UID
CHE-256.859.857
Founded
2021 · 5 years
Last commercial register change
September 6, 2021
Employees
1 to 10

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