Noga Brunicki
Management and Monitoring
of Clinical Trials
Tel : +972-77-2052400 Fax : +972-77-2052042 Mobile : +972-52-4532325 E-mail : contact@novatrials.com
Why NovaTrials
Local expertise - whether our clients are located in Israel or abroad, they need a reliable contact who is familiar with the internal administrative and procedural requirements of almost all Israeli sites. Having known the sites closely, NovaTrials posses an established 'know how' of internal requirements of each center. This enables us to demonstrate an efficient and reliable performance. We follow and track the internal specific requirements around clinical studies in each medical center on an ongoing basis and able to provide you with most updated consultation.
Quick response times – NovaTrials has a proven record of shortening study timelines in milestones like time to submission, ethics and regulatory approvals, site contract negotiations and approvals, site initiations, first subject randomized at each site etc.
Professional team - NovaTrials understands that at the end of the day, the site's cooperation and adherence to the clinical study requirements is strongly depending on the personally built relationship between the site contacts and the CRA. Our team is equipped with excellent communication skills and ability to develop strong working relationships.
High-quality services – NovaTrials is committed to GCP guidelines, the client's SOPs, local Israeli MOH requirements and intercompany procedures which we have developed to ensure your clinical trial will run safely and deliver a quality data.
Customer oriented approach – We strongly believe that each of our clients should receive the most relevant services based on their specific needs. Our medium size enables us to be non- bureaucratic and very flexible provider.
Reliable site feasibility process – We expertise on predicting the recruitment ability of a given MC based on an efficient feasibility process. We can ultimately asses any given study protocol for a preliminary detection of requirements and procedures that might delay or jeopardize the implantation of the clinical study. We face those challenges at a very early stage and work with our clients to find the most appropriate solutions.
Committed to deliver – Once engaged, NovaTrials will find and implement the most relevant supportive steps that will finally enable us to provide what we committed to. We will be responsible for building study awareness, networking for referral sources and also asses and manage the educational needs of institutions/sites regarding the study.