- Clinical Trial Services
Our team of experts and proven track record in the Region of South Eastern Europe make us a trusted partner in the field of Clinical Trials.
- Regulatory Affairs Services
Our Regulatory Affairs professionals with extensive experience across a full range of regulatory procedures are highly skilled in interfacing with regulatory authorities in all countries where we operate.
Our Pharmacovigilance professionals offer PVG support, which can include global and/or local PV services.
- Other services
We offer a wide range of services, supplementary to our main areas of activity.
- Quality assurance
We are able to provide you with a full range of independent GxP Quality Assurance Auditing, Consulting and Training for Pharmaceutical, Biotechnology and Medical Device products according to your needs.
We provide a range of services related to clinical development of new drugs and medical devices and all aspects of the registration process concerning medical products.