Regulatory Affairs, Pharmacovigilance, Medical Writing, Monitoring, Biostatics, Recruitment, Supplies, Quality Assurance, Project Management, Bioinformatics
Altiora operates in Central and Eastern Europe, having offices in Bosnia and Herzegovina, Croatia, Hungary, Macedonia, Poland, Serbia and UK.
Altiora has a team of well – educated, knowledgeable and experienced professionals, all of whom have worked within a clinical environment.
Working with a CRO, such as Altiora, will provide the chance to work in the dynamic, fast moving world of clinical research
Altiora is a Contract Research Organization (CRO), which operates in Central and Eastern Europe. We conduct phase I to IV clinical trials, for multinational pharmaceutical and biotechnology firms, as well as providing a broad range of related services. We understand and are experienced in the running of clinical trials, in compliance with Good Clinical Practice (GCP), using either our own SOPs or those of our clients. Today's complex and ever changing business/regulatory environment presents many challenges in the arena of clinical development, to which we are constantly adapting through our commitment to continuous improvement.