documentation

Documentation

Documentation for Multiple Packages

Documentation Relative to Medical Evacuation, Treatment and Cause of Death of Patients;

Documentation and Duties of the Parties Relating to the Carriage of Passengers, Baggage and Cargo

Documentation shall include, at a minimum, a comprehensive record of the site, including the provenance of underwater cultural heritage moved or removed in the course of the activities directed at underwater cultural heritage, field notes, plans, drawings, sections, and photographs or recording in other media.

The documents shall provide an insight into:

The documents must provide an insight into:

The documentation must also contain a customer declaration as referred to in Article 4.

It must also indicate the field of use of the component.

The documentation of consignments and labelling of these substances should be sufficiently explicit.

The file shall contain at least the information described under points 1, 2 and 3 below.

The dossier was referred to the Standing Committee on Plant Health on 2 February 2001.

The documentation may also be kept in the form of reproductions on an image medium or other data media.

PARTICULARS AND BATCHES OF LATCHES AND HINGES TO BE SUBMITTED BY THE MANUFACTURER OR HIS AUTHORISED REPRESENTATIVE.

The dossier shall contain all the administrative information and scientific and technical documentation described in Articles 12 to 14.

This quality system documentation must permit a consistent interpretation of the quality programmes, plans, manuals and records.

The quality system documentation must permit a consistent interpretation of the quality programmes, plan, manuals and records.

The quality system documentation must permit a consistent interpretation of the quality programmes, plans, manuals and records.

Documentation and correspondence in connection with EC examination procedures must be drawn up in the same language or languages as the instruction manual referred to in point 7.1.1 of Annex II.

The quality system documentation must permit a consistent interpretation of the procedural and quality measures such as programmes, plans, manuals and records.

The documentation and records referred to in paragraphs 1 to 4 shall be kept for at least three years from the end of the calendar year in which the transaction referred to in paragraph 1 took place, and must be readily available for inspection by the competent authorities upon request.

Documentation and labelling

Documentation & open sources

The safety documentation shall show:

Filing

Safety documentation A. O. Expert report

DOCUMENTATION FOR APPLICATIONS IN EXCEPTIONAL CIRCUMSTANCES

validation documentation for computerised systems;

Residue documentation B. 0 Expert report

It must be accessible to the notified body.

The documentation shall contain so far as relevant for assessment:

So far as relevant for the assessment, the documentation must contain:

The documentation must also contain a customer declaration as referred to in Article 4.

The quality system documentation shall contain, in particular, an adequate description of:

The documentation of consignments and labelling of these substances should be sufficiently explicit.

Documents for sale, transfer, or delivery in another Member State, or export

Documentation should be kept in a form that the company considers most effective.

The documentation on the quality-control system shall in particular include an adequate description of:

The dossier and the information from the review were also submitted to the Scientific Committee for Plants.

The file shall be held at the disposal of the competent authorities for 10 years following the placing of the PPE on the market.

The dossier was referred to the Standing Committee on Plant Health on 5 June 2001.

The dossier was referred to the Standing Committee on Plant Health on 18 October 2000.

the documentation must furthermore contain a declaration from the customer which shows the specific uses of the substances.

The documentation may also be kept in the form of reproductions on an image medium or other data media.

manufacturing and control file for each pharmaceutical form and a description of the method of dilution and potentiation,

The dossier on spinosad was referred to the Standing Committee on plant health on 17 August 1999.

The dossier and the information from the review have also been submitted to the Scientific Committee on Plants for consultation.

The dossier for EXP60707B (acetamiprid) was referred to the Standing Committee on Plant Health on 22 February 2000.

This quality system documentation must permit uniform interpretation of the quality programmes, quality plans, quality manuals and quality records.