Welcom to Medical Investigation & Research Inc,

M.I.R.I

Clinical Research Project management 

& Consulting 

                                                                                                                                        

"At MIRI Clinical Research & CRO, we provide tailored clinical trial project management services to meet the unique needs of each Investigator, CRO, Clinical Research Unit, and Clinical Research Directorate. Based in Le Pecq, M.I.R.I.CRO is an innovative  organization specializing in clinical research project management. Founded by two experts in the medical and pharmaceutical fields, our company offers a comprehensive range of services to support clinical research projects from conception to completion."

  • Founder: Nacim
    A physician with 15 years of experience as a coordinator and later manager in the surgery and outpatient sectors, as well as experience as a clinical research project manager at INSERM, Clinical investigation center, with previous roles at A.P.H.Paris and in the private sector.
    Graduate of the Clinical Research Project Manager program at Paris Descartes Medical School.

    Co-Founder: Nawel
    Doctor of Pharmacy and PhD in Biology, with experience at A.P.H.Paris and in private practice.
    Certified in pharmacovigilance and therapeutic monitoring, she has contributed to several clinical research projects and publications. Graduate of the Pharmacy School at Jussieu, Paris.

Services

Project Management

Complete management of clinical research projects, from planning to closure

  • Response to Calls for Proposals
  • Needs Analysis
  • Development of Detailed Proposals

Design of Protocols and Associated Documents

  • Protocol Writing
  • Creation of Participant Information Sheets
  • Development of Investigator Brochures

Translation of Protocols

  • Translation from French and Spanish

Registration on ClinicalTrials.gov

Methodology and Planning

  • Development of Monitoring Plans
  • Study Planning and Implementation
  • Site Closure and Database Lock

Site Selection

Our years of experience have allowed us to forge strong relationships with various departments such as medicine, surgery, microbiology, pharmacovigilance, genetics, etc.

Our extensive network of physician-investigators enables seamless communication with our collaborators due to these collegial ties.

Our deep understanding of the medical field allows for precise selection, resource alignment, and anticipation of site responsiveness.

Regulatory Compliance

  • ANSM (French National Agency for the Safety of Medicines and Health Products)
  • CPP (Ethics Committees for the Protection of Individuals)
  • CNIL (French Data Protection Authority)
  • CTIS (Clinical Trials Information System)
  • EudraCT (European Union Drug Regulating Authorities Clinical Trials)

Protocol Translation

  • Translation from French and Spanish
  • ClinicalTrials.gov Registration

Data Analysis

Advanced Data Analysis, providing clear and accurate reports for reliable and valid conclusions. We use the powerful Easymedstat eCRF, which enables analysis for scientific article publication.

  • Analysis of Collected Data
  • Interpretation of Results

Questions

How about your expertise?

I am a clinical research professional with extensive experience in clinical trials, medical devices, and project management. My expertise lies in ensuring compliance with regulatory standards (ICH-GCP, MDR, ISO 14155) while supporting investigators, CROs, and sponsors in the successful conduct of clinical studies.

Throughout my career, I have developed strong skills in:

  • Clinical trial coordination and monitoring – ensuring data quality, protocol adherence, and regulatory compliance.

  • Medical device clinical investigations – guiding teams through the specific requirements of MDR and ISO 14155.

  • Project management in clinical research – overseeing timelines, budgets, and multi-stakeholder collaboration.

  • Training & education – designing and delivering tailored programs to strengthen the skills of Clinical Research Associates (CRAs) and project teams.

I combine scientific rigor with a pragmatic approach, helping research teams and sponsors streamline their processes, reduce risks, and achieve high-quality outcomes.

"Thanks to MIRI Clinical Research Consulting, our clinical research project was conducted with exceptional precision and efficiency. Their expertise in project management was invaluable and allowed us to achieve our goals on time."

SFHG

Contact :

contact@miricro.com

For any questions or requests, please feel free to contact us using the form below.

Localisation

MIRI Clinical Research Consulting
7 Rue du petit marché

Poissy

 

Who Are We?
MIRI Clinical Research Consulting is a consulting firm specializing in clinical research project management. Based in Le Pecq, our mission is to provide high-quality support to our clients to ensure the success of their clinical research projects. Our team of experts has extensive experience in various areas of clinical research, allowing us to offer tailored solutions to meet the specific needs of each client. We are committed to maintaining the highest standards of quality, ethics, and compliance, while ensuring that every project is carried out with efficiency and precision.