Venn Life Sciences - Think Research

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Contract research services for clinical trials

We can deliver a broad range of clinical services depending on your trial specific needs.

Recruitment and evaluation of investigators:
Venn can perform feasibility studies to help evaluate your project and give you in-depth information about the market, resources and costs related to your specific trial.

We will use our network and experienced staff to target the investigational sites that fit your trial’s requirements.

Pre-study visits will be conducted by our highly qualified and experienced personnel to ensure the sites have adequate staff and facilities for your project.

GCP and Study Specific Training:
After we select the investigational sites, all investigators and site personnel receive GCP and study-specific trainings to ensure high quality data and procedures.

New trainees will receive coaching and the sites personnel will be re-trained when needed during the course of the study.

Submissions to country and local Ethics Committees:
Venn can support and manage your regulatory submissions in addition to all the necessary follow-ups to the relevant ethics committees.

Organisation of investigator meetings:
The Investigator meetings can be efficiently planned by our staff as part of our clinical services, including correspondence with the requested site staff and tracking of their attendance.

CRF design:
Our clinical staff are fully experienced with both paper and electronic forms. So we can assist in the design and implementation of your study-specific CRFs.

Additionally, we retain an EDC platform, which facilitates the design and implementation of eCRF. This can also work with a third party depending on your requirements.

Translations:
Venn has managed clinical trials across the globe.

We have established trusting business partnerships with competent translators in different languages (English, French, Spanish, German, Hebrew, Russian, etc).

And for translated documents to be submitted to the various ethics boards, we can provide translation and back-translation certificates.

Regular monitoring of phase I-IV trials:
Our clinical staff can perform thorough site management, including onsite monitoring.

Reporting to sponsor:

Communication of site and study status with the Sponsor is a key element for the study’s success.

Our SOPs precisely dictates the reporting procedures to our clinical staff, ensuring constant communication of updates to the Sponsor.