Impulsing the wellbeing of tomorrow
Research Institutions & Academic Societies
Research groups requires a very unique skill combination, in order to convert an initial concept into a final prototype. Our practical approach enables us to tackle your project efficiently and within time and budget.
In Time and On Budget
For a clear point of contact with the client and to ensure the highest level of service, we work on a single-contact basis, meaning that one project manager coordinates the integration of internal and external teams.
A good relationship between the project manager and the client is key to the success of the project overall. Your project manager will oversee the following:
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Scope of the work
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Time and cost expectations
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Coordinate the communication between the client and internal or external bodies
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Produce bespoke reports on study metrics
From Sample To Report
Our experience enables us to identify the best, most cost-effective way to complete your clinical trial. We can then offer quality data and insightful analysis to fit the client's needs. From start to completion we deliver a full line of services including:
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Development of biometrics design plan
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Customised case report forms (CRF's) to suit the study plan
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Electronic data capture tools (EDC's)
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Exploratory analysis
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Statistical reports
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Regulatory report submission, including summaries of safety and efficacy ​
Clinical Monitoring
Clinical monitoring is indispensable to ensure high quality data. We can fully take care of all aspects including:
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Site recruiting and trial
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Risk-assesment
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On-site and remote monitoring
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Site management
-
Staff support
-
Site visits
In Time and On Budget
For a clear point of contact with the client and to ensure the highest level of service, we work on a single-contact basis, meaning that one project manager coordinates the integration of internal and external teams.
A good relationship between the project manager and the client is key to the success of the project overall. Your project manager will oversee the following:
-
Scope of the work
-
Time and cost expectations
-
Coordinate the communication between the client and internal or external bodies
-
Produce bespoke reports on study metrics
From Sample To Report
Our experience enables us to identify the best, most cost-effective way to complete your clinical trial. We can then offer quality data and insightful analysis to fit the client's needs. From start to completion we deliver a full line of services including:
-
Development of biometrics design plan
-
Customised case report forms (CRF's) to suit the study plan
-
Electronic data capture tools (EDC's)
-
Statistical analysis
-
Regulatory report submission, including summaries of safety and efficacy ​
Clinical Monitoring
Clinical monitoring is indispensable to ensure high quality data. We can fully take care of all aspects including:
-
Site recruiting and trial
-
Risk-assesment
-
On-site and remote monitoring
-
Site management
-
Staff support
-
Site visits
We Speak Your Language
We can provide trusted medical translations from English into Spanish, to Clinical Research Organizations (CRO), pharmaceutical and biotech companies, manufactures of medical devices, scientific societies and clinical researchers.
We can translate of a wide variety of medical documents including:
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Adverse Event Source Documents
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Case Report Forms (CRFs)
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Informed Consent Forms
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Insert Leaflets
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Instructions for Use (IFUs)
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Patient Diaries
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Patient Recruitment Materials
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Patient Reported Outcome Measures
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Patient Source Documents, Admission and Discharge
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Pharmacological Studies
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QoL Scales
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Regulatory Documents
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Scientific Papers
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Study Protocols
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Suspected Unexpected Serious Adverse Reactions (SUSARs)
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