FARMOVS Support Services

Pharmaceutical services

Registered as a hospital pharmacy; preparation, packing and labeling of investigational medical products (IMPs); handling of controlled substances; storage and distribution depot of IMPs for multicenter Phase I – IV studies countrywide

Project and site Management

Single and multi-centre project management and national site management

Medical Writing

Study design, protocol, clinical study report and ICFs

Regulatory Service

Ethics and regulatory submissions of  clinical trial applications

Quality Assurance (QA) and Quality Management (QM)

Independent quality audits of various aspects within the life cycle of the clinical trial and vendor qualifications

Logistical Service

Import/export management of clinical trial  supplies(e.g. PK collection kit) and IP and PK sample storage

On-Site Archiving

According to ICH guidelines on good document practice

The FARMOVS team offers the full spectrum of clinical research services and comprises 160 full-time employees with extensive experience and expertise