(P.H.C & S) is an independent Clinical Research Consulting company who manages your clinical study from planning to clinical study report by offering 3 main services.

P.H.C & S knows how to run clinical trials with operational excellence in the most efficient and accurate manner within Europe. With regard to the broad and good knowledge of European health ecosystem in which clinical research can thrive; P.H.C & S acts as representee or coach namely for non-European clients in selecting appropriate sites and partners and if necessary, overseeing clinical activities. P.H.C & S provides its clients with excellence in trial performance, contributing to the development of new therapies and medicines across a broad range of conditions.

No standard plan, but customized solution tailored to your needs.

We eager to become your partner based on dedication and trust.

Interest to know more about us? Contact us at info@phcs.be

P.H.C & S guarantees you whole confidentiality and conformity with ICH-GCP, MDR, the European directives. 

P.H.C & S’ mission is to provide a comprehensive set of services to aid in the process of bringing new effective treatments (Drug or Medical Devices) to the market, through Clinical Trials namely phase I, II, III, IV and observational clinical trials.

Are you a Biotech, Start-up, (small size) CRO, ... located in Europe or outside of Europe and you are conducting Clinical Trials within Belgium, French, Luxembourg, Switzerland, or in some Africa countries? 

Are you looking for consulting or CRO services?

Are you looking for EU partners in the field of clinical research?

P.C.H &S can help you by:

  • Navigating the labyrinthine paths of European clinical research;
  • Adapting all Clinical Studies, essential documents to appropriate regulation;
  • Leading the study start up (regulatory authorization, contract negotiation...);
  • Performing visits (SQ, SIV, monitoring, close out...);
  • Connection with industry veteran;
  • Mapping of EU partners
  • Do you need internal training for your team?
  • Introduction to the conduct of Clinical Trial for MD (iso 14155);
  • Introduction to risk management (iso 14971)

Managing Director

25 years of experience working in Food, Medical Devices and Pharmaceutical industry with strong emphasis on Drug/MD development. Extremely experienced and have a detailed knowledge of ICH-GCP and MDR guidelines.

Proven track record for successfully setting the Clinical Development Strategy together with the medical and development teams.

Key to my role is being Strategic/Operational Leader of the medicine candidate’s strategy into realistic and executable operational plan.

Yearly budgets account to approximately 400 KEuros

Enthusiastic, high-energy achiever, team player.

Specialty: Biotech, budget, CE-marking, coaching, consulting, competent authority, clinical operational, clinical management, clinical trials, close out visit, CRF, CRO, CTR, CT Regulations, data management, drug development, efficacy, ethics committee, eCollect(EDC), Electronic Data Capture system, Digital Platform Technology for Life Science, english, eSAE, FDA, french, GCP, ICH, investigator, iso 14155, iso 14971, Medical Devices, MD, MDR, medical device regulations, monitoring, negotiation, pharmacovigilance, PIC, project management, quality, risk management, safety, Site initiation visit, start-up activities.