Global site
Czech Republic
Germany
Poland
Romania
Russia
Spain
United Kingdom
Investigators
|
Careers
|
Sitemap
|
Legal notice
Home
Company
About Accovion
Locations
Experience / Expertise
Careers
Legal notice
News & Events
Events
News
Industries
Pharmaceutical Industry
Biotechnology
Medical Devices
Services
Quality Assurance
Regulatory Consulting
Information Technology
Project Management
Medical Writing and Electronic Publishing
Medical Services
Clinical Data Management
Clinical Trial Management
Clinical Monitoring
Health Outcomes Research
Pharmacovigilance
Statistical Programming
Biostatistics
Accovion Plus
Publications
View all
Brochures
Case Studies
Press Releases
Presentations
Contact
Contact Form
Info
Investigators
Careers
Sitemap
Legal notice
Print
E-Mail this page
Feedback
Info
>
Sitemap
Company
About Accovion
Locations
Experience / Expertise
Careers
Job opportunities
Oportunities Base
Legal notice
News & Events
Events
News
Industries
Pharmaceutical Industry
Biotechnology
Medical Devices
Services
Quality Assurance
Regulatory Consulting
Clinical Trial Submissions
Regulatory environment
Accovion opens the door to Europe for you
Statistical consulting
Scientific advice support
Ethical and regulatory guidance
Clinical development plans
DMC, DSMB, EPV and more
Drug safety consulting
Specific indications and populations
Information Technology
Project Management
Effective project management
Accovion's project manager
Medical Writing and Electronic Publishing
Development and writing of documents
Electronic compilation and hyperlinking
Electronic submission
Management, standardization and training
Medical Services
Feasibility
Medical monitoring
Clinical Data Management
CRF design
Database design and programming
Integration of data from other sources
Coding
Data validation
Electronic Data Capture
Paper CRF
Data management status and tracking reports
Patient reported outcome (PRO) data
SAE reconciliation
Clinical Trial Management
Training and familiarization
Management of vendors and external partners
Meetings
Trial master file
Contract and grant management
Clinical Trial Management System (CTMS)
Logistics (IMP, device and other materials)
Clinical Monitoring
Accovion clinical monitors
Monitoring concepts
Patient recruitment and retention
Health Outcomes Research
Pharmacovigilance
Clinical Trials and Post Marketing
Special solutions for estabilshed PV department
Risk management consultancy
IT Infrastructure and safety DB
Statistical Programming
Data preparation and TLGs/TLFs programming
Virtual Linux SASĀ® programming environment
Data integration for pooled analysis
CDISC data conversion and consulting
Regulatory submission support
Pharmacokinetics analysis
Graphical patient profiles
Biostatistics
Biostatistical expertise
Accovion statistical services at a glance
Accovion Plus
Publications
Contact
Contact Form
Info
Investigators
Careers
Sitemap
Legal notice
Last viewed
Sitemap