Basic info
Industry
biotechnology research
Sectors
Safety Adverse Event (SAE) Management
GPV
GMP QA
Clinical Trials
Inspection Readiness
Clinical & Medical Consulting
GDP
Medical Writing
Medical and Safety
GCP QA Expertise
Pharmacovigilance in Europe
Clinical Monitoring and Site Management
Regulatory Consulting
eTMF Management
GMP
Auditing for GLP
QMS Implementation and Auditing
Remediation for Clinical Inspections
Project Management
GCP
Clinical Trial Planning
Consulting
Patient Recruitment
Statistical Consulting
Biopharma
Biannual Inspections
Date founded
2010