Our commitment to you does not end with a digital trial solution. Our education and support services are developed to make sure your team has a great experience with our technology and our personnel.
All Precerche clinical personnel have been thoroughly trained on the conduct of pre-study site visits as well as numerous other pre-study activities. Additionally, Precerche Clinical Research Associates (CRAs) have a minimum of ten years monitoring experience.
Precerche offers complete services in the area of initiating the conduct of clinical trials at the conclusion of, or in conjunction with, study start-up activities. Precerche clinical managers have initiated studies in a wide variety of therapeutic indications.
Conduct of clinical studies involves specific monitor knowledge and experience in reviewing on-site regulatory documentation, informed consent documents, and patient records. The monitor’s general responsibilities also include sStudy drug dosage calculation, verification, reconciliation, and inventory.
Precerche provides high-level experienced Project Managers for a wide variety of clinical study managerial tasks. Precerche Project Managers have extensive experience in a number of therapeutic areas.
In the world of pharmaceutical, biotechnology and medical device development, the journey from the bench to the patient can be long and arduous. Throughout the research process, information must be clearly disseminated to a variety of individuals, from investigators to regulatory agencies to research subjects enrolled in clinical trials.
Precerche provides full services related to study close-out activities as either a stand-alone service or as part of the conduct of a clinical study that Precerche is supporting.
Precerche takes great pride in the experience with Regulatory, Quality Assurance, and Compliance requirements. In addition to regulatory and quality assurance services in support of the conduct of a clinical study, Precerche also provides these services on an ad-hoc basis at the request of sponsor companies.
Training is essential at study start, but can continue through the life of the engagement -- whether to refresh or to introduce new personnel to InterRx. The available training is to further ensure that all participants in the digital trial - whether using DataManager, Lifecycle, or InterRx CRO - have the latest information about the technology or the trial itself. Our goal is to provide the best in customer service.
Digital training and support include:
Additional options include:
To arrange a demo of InterRx Lifecycle or for more information on InterRx CRO, contact us.