Itec services

Epidemiological study management

ITEC SERVICES stands on two decades of pre-marketing experience in clinical trial management and offers you effective skills in the design, conduct and follow-up of epidemiological studies.

There is no conceptual difference between Pre- and Post-Marketing studies except for adequate methodology and means.

The aim of ITEC SERVICES in this discipline is to: Encourage medical marketing decisions based on empirical observations and scientific evaluation

Strategic development advice:

ITEC SERVICES can contribute to the development of your product by virtue of its:

• expertise in diseases and the clinical environment
• mastery of appropriate methodologies
• expert groups and partners able to lobby opinion leaders
• certified technology (e-CRFs reporting on-line with secured access)
• communications (newsletters) sent to investigators during a study.

Study designs and methods:

• Cohort and case studies: recording the incidence of a disease during a defined period.
• Real-life assessments: cross-sectional and longitudinal studies of outcomes after medical interventions, as reported by patients.
• Patient population studies: recording frequencies of prescriptions, drug consumption, patient characteristics, concomitant treatment, and related drugs.
• Product documentation (prospective and proactive): retrieving and summarising the literature on long-term risks and benefits of treatments, or procedures, in patients with a given diagnosis.

ITEC SERVICES offers specific solutions to your projects

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Design/Creation:

ITEC SERVICES and its partners bring creativity and experience in visual impact to your epidemiological studies, giving them a distinctive ‘look’.
Our strengths:

• Creative flare
• Knowledge of patients as consumers
• Knowledge of the healthcare sector (community and hospital)
• Deployment of resources (designers, artists, pre-release, press …),
• Scientific interaction
• Direct involvement in all these activities

Administrative procedures:

ITEC SERVICES is fully conversant with relevant regulations and guidelines, ensuring an optimal start to epidemiological studies.

Implementation and follow-up of studies:

We work with you, side-by-side, at all conceptual stages of planning an evidence-based clinical strategy. Our proposals for post-marketing trials embody your marketing and commercial objectives.
Our teams and procedures (technical and logistic) convert with ease new post-marketing results into clinical updates for yourselves, the sales force, and your prescribers.

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