Public-Private Partnerships (PPPs) consist of joint initiatives between the private sector (i.e., pharmaceutical companies, small-medium enterprises…) and public sector (i.e., universities, public health institutes, research organizations) in which resources and responsibilities are shared in order to achieve a common goal. This cooperative arrangement follows tailored governance models, which clearly define the roles and responsibilities of the stakeholders, ensure complete transparency of their interactions and guarantee robustness and scientific value of the studies performed.

Benefits of Public–Private Partnership
Past and present health crises have highlighted that an efficient collaboration between the public and private sector is essential to address major health challenges. The main benefits of a PPP are the sharing of resources (e.g., economic funds, health infrastructure, knowledge and experience in disease and related vaccine and study designs, patients data and samples), risks, responsibilities, and rewards. PPPs foster collaboration and create multi-disciplinary networks of scientific experts.

Colleagues connecting jigsaw pieces together


id.DRIVE is a PPP funded by the pharmaceutical company partners leveraging health capacities from public partners and sites. It follows key guiding PPP principles collaboration aiming to:

  • promote scientific exchanges between several stakeholders with various expertise
  • optimally steer joint efforts towards the desired outcome within the time and resource constraints
  • allow efficient decision-making, and guarantee scientific integrity of the study results with high quality standards.

id.DRIVE Governance structure is reflected in the following diagram:

id.DRIVE Governance structure.

id.DRIVE is based on the following principles: 

  • The Steering committee decides on the study platform strategic direction, allocations of funds and resources for the studies.
    The steering committee is composed of representatives from id.DRIVE partners. Decision authority is split equally between non-industry and pharmaceutical companies.
  • Master scientific and technical documents are developed by scientific experts from id.DRIVE partners.
  • Scientific review of the master and study specific scientific documents is overseen by the Independent Scientific Committee (ISC) (see section below for ISC members).
  • Quality control management and audit of the partnership and studies are overseen by the Quality assurance and audit committee (QAAC), composed of quality assurance experts from the pharmaceutical companies.
  • At the study level, decision making and study conduct are the responsibilities of the corresponding Study Team (ST).
  • Data collection is carried out at several independently operating Study Sites which constitute the study network. P95 is the sponsor of the studies. Study Sites remain owners of their data. Pharmaceutical companies’ partners are not permitted access to the data.

The id.DRIVE Governance Charter is available upon request, contact us at info@iddrive.eu

Independent Scientific Committee

To increase the robustness and transparency of the scientific results produced by the partnership, the scientific leadership of id.DRIVE is supported by an Independent Scientific Committee (ISC). The ISC’s mandate is to review and provide recommendations on the master and study-specific scientific documents.

The current members of id.DRIVE ISC are:

Dr Gabrielle Breugelmans
Head of Epidemiology of The Coalition for Epidemic Preparedness Innovations (CEPI), an international alliance to finance and coordinate the development of new vaccines for the prevention and containment of infectious disease epidemics. She is an infectious disease epidemiologist with broad expertise in global health, poverty-related diseases and vaccinology in low- to middle-income countries. She holds a PhD and Master of Public Health degree in Epidemiology from the Johns Hopkins Bloomberg School of Public Health in the U.S., and a Master’s degree in Health Sciences from the University of Maastricht in the Netherlands.
Prof. Elisabeth Miller
Consultant Epidemiologist and former Head of the Immunisation, Hepatitis and Blood Safety Department of Public Health England. She has extensive experience in studies of risks and benefits of vaccination programmes and specific vaccines. Her other interests include seroepidemiology, mathematical modelling, and viral infections in pregnancy. She was a founding member of the WHO Global Advisory Committee on Vaccine Safety and served as a member of the WHO Strategic Advisory Group of Experts (SAGE), chairing working groups on pertussis, polio and influenza.