Atlant Clinical Services

We provide a comprehensive range of services in clinical trials:

Medical writing and document validation:

• Clinical Study Protocols, Case Report Forms
• Informed Consent Forms, Patient Information Sheets
• Clinical Study Reports (Phase I – IV)
• Investigator Brochures and updates

Clinical trial monitoring and project management:

• Identification, qualification and initiation of trial sites
• Ongoing monitoring, recruitment enhancement
• Data verification, compliance control, drug accountability, site closure
• Study supplies import & export management
• Financial management
• Site logistics management
• QA & QC
• Data Management & Statistics
• Study Drug Warehouse, Central Laboratory*

Study regulatory support:

• Dossier preparation & consultancy
• Regulatory approval
• Periodic regulatory communication, safety reporting
• 98% of submissions to regulatory authorities ended with approval

  * Via partners and subcontractors

To find out more about services rendered by Atlant Clinical, please visit our web site: www.atlantclinical.com