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DirectoryBusiness & Technical ServicesManagement ConsultingBôleObelysQ SA
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ObelysQ SA

Summary

About the company

The core activity of ObelysQ is to provide consulting services to the pharmaceutical industry, particularly in the area of clinical trials. This includes: GCP consulting (Good Clinical Practice), GCP and GVP audits (Good Clinical Practice and Good Vigilance Practice), development of Standard Operating Procedures (SOPs), preparation and support for inspections by health authorities, training and training for employees in the GCP/GVP area, conducting gap analyses to identify areas for improvement, support for the implementation of EU-CTR (European Clinical Trials Regulation), data protection support, and review of audit reports and CAPAs (Corrective and Preventive Actions). The company thus offers comprehensive consulting services to improve compliance and quality of clinical trials in the pharmaceutical industry.

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Industry:Management Consulting
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Research & Development
✓ Offered7
QA consulting
GCP consulting, senior-level quality assurance support, compliance across clinical activities, inspection readiness from early development through late-phase trials.
GxP Auditing
GxP audits across therapeutic areas and development stages, worldwide audit execution, regulatory and operational audit support.
QMS / SOP development
Development and update of quality management systems and SOPs, lean quality systems, procedural frameworks for clinical programs.
Inspection Management
Inspection readiness assessments, on-site inspection management, post-inspection remediation for EMA, FDA, MHRA, Swissmedic and other authorities.
Training
Regulatory training sessions with examples and case scenarios tailored to function and company structure, latest compliance and regulatory updates.

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Location

Rue du Temple 36
2014 Bôle

At a glance

Legal form
Corporation
UID
CHE-314.855.618
Founded
2020 · 6 years
Last commercial register change
April 7, 2025
Employees
1 to 10

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