MTH Booking
Benefit from a service through
a network of resources
MTH Booking, the tool to accelerate your
projects with qualified resources
In an environment where deadlines are tight, unforeseen events are frequent and regulatory pressure
is constant, operational responsiveness has become a key issue for those involved in clinical research.
Quickly identifying a competent, available and qualified resource is often a challenge.
MTH Booking is an innovative solution designed to address this issue: it allows you to request a
resource immediately available. Whether you need to reinforce a team, plan an activity or obtain a
deliverable, you benefit from a pool of qualified resources.
In today’s competitive clinical research environment, organizations often face the challenge of quickly finding the right expertise, mobilizing reliable teams, or producing high-quality deliverables under tight regulatory constraints. Our solution offers you immediate access to specialized consultants and services, designed to match your operational needs and accelerate your projects.
- Assignment of talent: are you looking for an CRA to conduct several visits in France or Europe? Find the consultant with the required expertise;
- Provision of a service: do you have an on-site audit to assess GCP compliance coming up? Request a team that can support you throughout the entire mission;
- Production of deliverable : do you need to draft a clinical study protocol? Receive your document in compliance with regulatory requirements.
Whether you need to strengthen your team, secure regulatory compliance, or deliver critical project documentation, our network of experienced professionals is at your disposal. With a flexible and responsive approach, we help you gain efficiency and ensure the success of your clinical research activities.
In clinical research, organizations frequently face urgent and diverse needs: strengthening teams with the right expertise, preparing for regulatory inspections, or producing compliant documentation. Our flexible service model is designed to meet these challenges by giving you direct access to qualified consultants, specialized teams, and regulatory-grade deliverables.
- Assignment of talent: are you looking for an CRA to conduct several visits in France or Europe? Find the consultant with the required expertise;
- Provision of a service: do you have an on-site audit to assess GCP compliance coming up? Request a team that can support you throughout the entire mission;
- Production of deliverable : do you need to draft a clinical study protocol? Receive your document in compliance with regulatory requirements.
From operational reinforcement to regulatory support, our solution provides the expertise you need, when you need it. With a trusted network of professionals, we help you accelerate timelines, ensure compliance, and secure the success of your clinical research projects.
Our quality commitments
