Sentence examples for the documentation will from inspiring English sources

Access to randomization codes during the phase of blinding will be monitored and documented and the documentation will be kept in the "CTMS (Clinical Trial Management System)".

The documentation will be posted on the official campaign page.

The documentation will allow them to manage certain affairs, such as making emergency medical decisions or enrolling their children in school, without the approval of a man — a limited but significant power in a country where women are still banned from driving and must have a male legal guardian for their entire lives.

The documentation will include the results on the comprehensibility of the information material assessed during the pre-tests and also the results of the piloting phases.

The documentation will act as important data material to be used in follow-up conversations and interviews related to each of the observed patients and in general to evaluate the quality of written documentation.

The documentation will consider each project phase individually and include a detailed log of the activities required during the phase and the resources required (hardware, software, expertise, programmer time, librarian time, user time).

Many cruise lines allow extended stopovers and this documentation will prove the legality and length of your stay.

Furthermore, the prime therapist is the one who will document on the session documentation, will set goals with parents and is the contact person for the researchers.

As soon as written consent is obtained, patients can be included into the trial and the required documentation will be provided by the study centre (Studienzentrale Klinische Radiologie, Abt. Strahlentherapie und Radioonkologie, INF 400. 69120 Heidelberg).

As soon as written consent is obtained, patients can be included into the trial and the required documentation will be provided by the study center (Clinical Trial Center, Department of Radiooncology, University of Heidelberg Medical Center).

The study documentation will be maintained for at least 2 years after the end of the study so that they can be monitored, audited or inspected by the sponsor, the sponsor's authorised representatives or local regulatory authorities.