Our Services

  • 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.

  • Pharmacovigilance

    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.

About Us

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.

Map We are present in 8
countries of Europe