Quagilys Team

Quagilys Associés:

Seeks information about the real underlying needs of the clients, beyond those expressed initially. Pedagogical approach.
Over 25 years experience in pharmacovigilance and clinical quality management
Expertise: specialist in PV and regulatory processes of pharmaceutical sites, interest in complex situations requiring a global approach of processes
Professional background: 5 years in the pharmaceutical industry (QA Department), 22 years as a consultant
Pharm. D and Masters Degree in Pharmaceutical Quality Management

A pragmatic and project-oriented approach, quickly adapts to new situations and challenges
Over 20 years of experience working in the pharmaceutical sector, providing support to clinical research teams on audits, clinical quality management and training projects
Expertise: operational experience in clinical studies management, leading transversal projects, consulting in computerized systems validation and a keen interest in biometry processes
Professional background: 7 years in the pharmaceutical industry (Clinical Operations), and 13 years as a consultant
Masters degrees in Neurobiology – in Project and Business Management

A pedagogical approach, and a critical mind to assist clients on their projects
Has been supporting quality and clinical operations departments for 15 years, and has been training teams to develop a practical approach to quality management
Expertise: highly experienced in clinical operations, mentoring, appetite for complex situations requiring innovative solutions
Professional background: 13 years in a CRO (Clinical Operations), 20 years as a consultant
Pharm D. and postgraduate Degree in Biotechnology

Provides customized solutions to meet client needs, and has a constructive and collaborative project management approach
Highly experienced in clinical research (over 20 years), supporting operational teams, developing Quality Management Systems and delivering training focused on a pragmatic approach
Expertise: implementation of QMS, consulting in the ISO9001 certification process, operational experience in phase I clinical trials
Professional background: 15 years in clinical research (investigational sites and academic sponsors), 5 years as a consultant
Masters degree in Biochemistry, postgraduate degrees in Quality Assurance and in Toxicology