single-point information

signaling information | signalling information

lone signal unit | one-unit message | LSU [Abbr.]

tone paging

pure signaling instrument

mere non-disclosure [ simple non-disclosure ]

primary signalling information

Signage Supply Information System

advisory message | message

To add to the information on capital requirements, our notes say that the work is related to bridge rehabilitation, signalling systems, equipment contracts, track improvements, station repairs and information technology.

The Privacy Commissioner comes along and says potentially you're divulging third-party information now by putting that flag there, because the method by which you determine that the person hadn't had any contact, and therefore may have been deceased, that very act in and of itself may divulge information that is personal.

(24) In order to ensure uniform conditions for the implementation of this Regulation, implementing powers should be conferred on the Commission for the purposes of adopting implementing acts concerning detailed rules on the visibility of commercial brands during product demonstrations or tastings and on information and promotion material and on the visibility of the origin of products on information and promotion material; the annual work programmes , the selection of simple programmes , detailed rules under which a ...[+++]proposing organisation may be authorised to implement certain parts of a simple programme itself, the arrangements for the implementation, monitoring and control of simple programmes; the rules concerning the conclusion of contracts for the implementation of simple programmes selected in accordance with this Regulation; the common impact assessment framework for programmes as well as a system of indicators .

This report not only endorses the Commission’s proposed changes but also enhances them in some areas, including: strengthening the role of the Pharmacovigilance Risk Assessment Advisory Committee, which must have the power to recommend action to the Committee for Medicinal Products for Human Use; strengthening the role of healthcare professionals in the sense of voluntarily reporting adverse drug reactions; strengthening the role of patients in reporting adverse reactions directly; requiring that all adverse drug reactions (and not just serious ones) are reported to the Eudravigilance database by competent authorities and companies, which m ...[+++]eans that information on all adverse drug reactions will, for the first time, be centralised in one place in the EU; and requiring patient information leaflets that give a clearer indication of the main features of the drugs.