Guidelines for Consumer Advertising Guidelines for ...

Guidelines for Consumer Advertising of Health Products 5 1.5 Directions for Use When depicted or described, directions for use, dosing and product administration must be consistent with the TMA. EXAMPLE TRAVEL VACCINE Authorized Indication/Use: Part III – Consumer Information – Helps prevent Disease X. Protection against Disease X starts

  Information, Consumer, Consumer information

December 2012 GUIDANCE DOCUMENT FOR COMPETENT …

This guidance is, in general, also applicable for the nutrition labelling of foods under Regulations (EC) No 1925/2006/EC of the European Parliament and the Council on the addition of vitamins and minerals and of certain other substances to foods5 and No 1924/2006 of the European Parliament and of the Council of 20 1 OJ L 165, 30.4.2004, p. 1–141

  Regulations, Applicable, Labelling

Guidelines for the Safe Transport of Infectious Substances ...

These guidelines are applicable to the transport of infectious substances and ... The international regulations for the transport of infectious materials by any ... Labelling of the outer package for the shipment of diagnostic specimens must include the following.

  Regulations, Applicable, Labelling, Are applicable

Understanding the Safe Food for Canadians Regulations

applicable federal food legislation and regulations For more information refer to following CFIA web pages: Regulatory compliance, What to expect when inspected, and Compliance and enforcement. 14. Provincial and territorial authorities continue to enforce their applicable legislation for food. This will not change as a consequence of the SFCR.

  Regulations, Applicable

Principles of Labelling for Medical Devices and IVD ...

In some jurisdictions, “labelling” is referred to as “information supplied by the manufacturer”. Labelling includes the label, instructions for use, and information related to the identification, technical description, intended purpose and proper use of the medical device and IVD medical device, as applicable (Figure 1).

  Applicable, Labelling

Annex 9 Guide to good storage practices for pharmaceuticals

date. Where national regulations prescribe that records must be re-tained for a certain period, this must be observed. (Otherwise such records should be retained for a period equal to the shelf-life of the incoming materials and products, where applicable, plus 1 year). 5.4 Comprehensive records should be maintained showing all rece ipts

  Good, Practices, Pharmaceutical, Regulations, Storage, Applicable, Good storage practices for pharmaceuticals

ICH guideline E2F on development safety update report

efficiency. Some national and regional laws and regulations also require a periodic report that describes the status of ongoing individual investigations, manufacturing changes, and overall development status and plans. To be broadly useful, the DSUR should also include this information, in addition to safety-related information.

  Regulations

MANDATORY LABELING REQUIREMENTS

Page 2 8/2/2018 Overwrapped, Sleeved, or Case Containers: All mandatory labeling information must be placed on the top panel or information panel. No mandatory labeling requirements may be placed on the bottom panel. Information Panel: FDA - 21 CFR 101.4 The information panel as it applies to packaged food means that part of the label immediately contiguous and to