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Bring new drugs to the market requires thousands of documentation pages to accurately capture timely clinical test information. Errors can lead to lost time and money and put the development considerably again.
For Synteract, we are trying to deliver implementable results to tackle your clinical test requirements. Our medical writing group consists of qualified phds and other experts, and our European medical writers are all members of the European Medical Writer Association. Our team involves native speakers with many years of experience with many years of experience that translate all documents necessary for the fulfillment of clinical trials. They are managed by global standard operations and work closely with physicians, biostatisticians, pharmacokinetics and regulatory specialists. Our high-quality verification team continuously ensures the highest standards and compliance with planes and regulatory guidelines.
Whether a first clinical protocol, a PIVOTAL test protocol, or associated documents such as the ICF, the brochure of the investigator or a full IND / IDE, Syteract's team brings the therapeutic, clinical, regulatory and writing know-how required To ensure quality documentation for the success of your clinical trial from the design phase to the final regulatory template.
From the creation of documents to electronic document production and regulatory publication - we offer robust, reliable medical write support to accelerate applications and approvals. Our medical write services are offered as an integral part of our clinical development expertise or as a standalone service, each strategy tailored to customer requirements. With the high volume of documents required in clinical trials, we often offer a medical writing by a functional service alliance (FSA) with a dedicated team to assess the reporting result and creating messaging efficiency. We use innovative technologies and work with customers to determine optimal communication channels to keep them up to date every step of the way.
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