outsourcing and recruitment agency
Tailor-made outsourcing for your projects
A benchmark player in Life Sciences
of experience
complementary
A flexible, specialized offering for your projects
Key expertise for your projects
R&D
R&D covers all activities aimed at discovering, developing and improving new drugs, medical devices and therapeutic solutions.
- Preclinical research and development of molecules or devices
- Drafting experimental protocols
- Management and follow-up of feasibility studies
- Coordination between laboratories, partners and scientific teams
Regulatory and medical affairs
This function ensures that healthcare products comply with national and international regulatory requirements throughout their life cycle.
- Preparation and submission of authorization files (marketing authorization, CE marking, etc.)
- Regulatory watch and document update
- Interface with health authorities (ANSM, EMA, FDA)
- Drafting of medical and promotional documents in compliance with regulations
Clinical operations
Clinical Operations oversees the implementation of clinical trials, from planning to field follow-up, to ensure data quality and compliance.
- Study management (set-up, monitoring, closure)
- Selecting and training investigators
- Patient follow-up and clinical data capture
- Coordination between promoters, CROs and medical teams
Quality assurance
Quality Assurance ensures that processes, systems and documents comply with Good Practices (GCP, GMP, GLP) and pharmaceutical industry standards.
- Setting up and monitoring the quality system
- Management of regulatory audits and inspections
- Drafting and updating procedures (SOP)
- Training teams and raising their awareness of quality culture
Biometrics
Biometrics covers the statistical analysis and management of clinical trial data, essential for the scientific validation of results.
- Data management and database cleansing
- Statistical analysis and modeling
- Reporting and statistical reports
- Methodological support for clinical and medical teams
Vigilance
Pharmacovigilance, Matériovigilance, Cosmétovigilance, Nutrivigilance... Vigilance ensures the monitoring, collection and analysis of undesirable effects linked to health products, to guarantee their safe use.
- Collection and evaluation of adverse event reports
- Drafting of periodic safety reports (PSUR, RMP, etc.)
- Post-marketing monitoring and follow-up
- Communication with health authorities
Market Access & HEOR
Market Access & HEOR helps guarantee market access for healthcare products, by combining pricing strategy, reimbursement and relations with institutional players.
- Developing a product access and promotion strategy
- Preparation of price and reimbursement files
- Medico-economic analysis and cost-effectiveness studies
- Interaction with authorities and payers
IT
Our experts develop, test and deploy technological solutions that meet the requirements of the healthcare sector.
- Development and integration of business applications (e-CRF, EDC, LIMS, patient monitoring tools, etc.).
- Quality testing and validation (QA, GxP) of healthcare systems and software
- Deployment and automation (DevOps)
- Data management and security
- Maintenance and technical support to guarantee infrastructure reliability
A daily commitment to innovation
This platform allows you to formulate a detailed request so that our teams can respond immediately to your needs.
Whether it's a short mission, a one-off reinforcement or targeted expertise, we offer you a rapid, tailored response to support your projects.
Valérie HERVE, Business Manager, presents TempoPHARMA, the outsourcing and recruitment agency specialized in Life Sciences.
Find out more about our expertise
The strength of a multidisciplinary group
