There are changes to the advertising of medical devices

The draft regulation specifies:
1) the necessary data contained in the advertisement addressed to the public - in order to ensure that recipients receive appropriate knowledge about the advertised product, and which will be included in the instructions and labeling of the product;
2) the manner of presenting advertising of medical devices - analogous to the forms of presenting advertising of medicinal products, along with an appropriate warning issued or placed with the advertisement, and with the restriction of the forms of advertising in pharmacies and medical entities in order to enable the proper provision of services in these places.

In order to ensure the transparency of product advertising, § 5 of the draft introduces an obligation to inform about all benefits received, both tangible and intangible, in the case of advertising referred to in Art. 58 sec. 1 items 1-3 of the Act.

Project: HERE

Source: RCL