Act No. 25 / 2006 Coll.
Act amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended, and Act No. 132 / 2003 Coll., amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended
Valid
Effective from 26.01.2006
Zobrazeno prvních 200 z celkem 258 ustanovení tohoto předpisu.
Zobrazit celý předpis →
Pro stažení celého znění použijte tlačítko Stáhnout výše.
25
THE LAW
of 21 December 2005
amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended, and Act No. 132 / 2003 Coll., amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended
Parliament has decided on this law of the Czech Republic:
Amendment to Act No. 40 / 1995 Coll.
Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the Operation of Radio and Television Broadcasting, as amended, as amended, Act No. 258 / 2000 Coll., Act No. 231 / 2001 Coll., Act No. 256 / 2001 Coll., Act No. 138 / 2002 Coll., Act No. 320 / 2002 Coll., Act No. 132 / 2003 Coll., Act No. 217 / 2004 Coll., Act No. 326 / 2004 Coll., Act No. 480 / 2004 Coll., Act No. 384 / 2005 Coll., and Act No. 444 / 2005 Coll., is amended as follows:
1. In Section 1, the following paragraph 1 is inserted:
"(1) This law incorporates the relevant provisions of the European Communities (1) in the field of the regulation of advertising misleading, comparative, tobacco products, medicinal products for human use, veterinary medicinal products, food and infant formulae and follow-on formulae, and regulates the general requirements for advertising and dissemination, including penalties for infringements under this law and the designation of supervisory authorities. It also provides for the regulation of advertising on a specific offer as well as advertising on alcoholic beverages, on plant protection products, on firearms and ammunition and on funeral activities.
1) Council Directive 84 / 450 / EEC of 10 September 1984 on the approximation of the laws, regulations and administrative provisions of the Member States relating to misleading advertising, as amended by Directive 97 / 55 / EC of the European Parliament and of the Council of 6 October 1997 amending Directive 84 / 450 / EEC on misleading advertising to include comparative advertising. Article 7, 8 and 9 of Commission Directive 91 / 321 / EEC of 14 May 1991 on infant formulae and follow-on formulae, as amended by Commission Directive 1999 / 50 / EC of 25 May 1999 amending Directive 91 / 321 / EEC on infant formulae and follow-on formulae (Text with EEA relevance), Commission Directive 2003 / 14 / EC of 10 February 2003 amending Directive 91 / 321 / EEC on infant formulae and follow-on formulae (Text with EEA relevance) and Directive 96 / 4 / EC amending Directive 91 / 321 / EEC. Article 2 of Directive 2000 / 13 / EC of the European Parliament and of the Council of 20 March 2000 on the approximation of the laws of the Member States relating to the labelling, offering for sale and advertising of foodstuffs, as amended by Commission Directive 2001 / 101 / EC of 26 November 2001 amending Directive 2000 / 13 / EC of the European Parliament and of the Council on the approximation of the laws of the Member States relating to the labelling, marketing and advertising of foodstuffs and Commission Directive 2002 / 67 / EC of 18 July 2002 on the labelling of foodstuffs containing quinine and foodstuffs containing caffeine (Text with EEA relevance). Article 2, 3, 4, 5 and 10 of Directive 2003 / 33 / EC of the European Parliament and of the Council of 26 May 2003 on the approximation of the laws, regulations and administrative provisions of the Member States relating to advertising on tobacco products and sponsorship related to tobacco products (Text with EEA relevance). Article 86, 89, 90, 91, 94, 95 and 96 of Directive 2001 / 83 / EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use, as amended by Directive 2002 / 98 / EC of the European Parliament and of the Council of 27 January 2003 laying down quality and safety standards for the collection, testing, processing, storage and distribution of human blood constituents and amending Directive 2001 / 83 / EC and Commission Directive 2003 / 63 / EC of 25 June 2003 amending Directive 2001 / 83 / EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use (Text with EEA relevance) and Directive 2004 / 27 / EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001 / 83 / EC on the Community code concerning medicinal products for human use (Text with EEA relevance). Article 85 of Directive 2001 / 82 / EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products, as amended by Directive 2004 / 28 / EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001 / 82 / EC on the Community code relating to veterinary medicinal products (Text with EEA relevance). Article 6 of Council Directive 89 / 398 / EEC on the approximation of the laws of the Member States relating to foodstuffs intended for particular nutritional uses. Article 9 (2) (c) of Council Directive 80 / 777 / EEC of 5 July 1980 on the approximation of the laws of the Member States relating to the exploitation and sale of natural mineral waters. Articles 69, 94 (2) and 100 of Directive 2004 / 27 / EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001 / 83 / EC on the Community code relating to medicinal products for human use (Text with EEA relevance). '
Paragraphs 1 to 7 shall be renumbered paragraphs 2 to 8.
footnote 1 shall be renumbered footnote 1a, including the footnote reference.
2. § 2a, including footnote 8, reads:
Comparative advertising for medicinal products intended for human use (hereinafter referred to as "medicinal products for human use ') or for medical care is permitted, subject to the conditions laid down by special legislation7) if it is aimed at persons authorised to prescribe or dispense such medicinal products (hereinafter referred to as" professionals') or to provide such healthcare.
8) Act No. 20 / 1966 Coll., on the Care of People's Health, as amended. Act No. 160 / 1992 Coll., on Health Care in Non-State Medical Devices, as amended. Act No. 79 / 1997 Coll., on medicinal products and on amendments and additions to certain related laws, as amended. '
3. § 2b, including the title and footnote 9, reads:
Advertising indicating a specific offer
(1) An advertisement indicating a specific offer of goods shall be prohibited in cases where the seller (9) is known to the processor or the advertiser (s), or may assume that he is not or will not be able to secure the goods offered in a quantity corresponding to the expected demand, taking into account the extent or manner of the dissemination of advertising, the nature of the goods or the price offered, or if he does not indicate in the advertisement the quantity of goods offered in the special offer at each establishment for sale.
(2) An advertisement indicating a specific tender must clearly state the date on which the tender ends. If the special offer has not yet started to apply on the date of publication of the advertisement, the date of the start of the period during which the special price or other conditions will apply shall also be indicated in the advertisement.
9) Paragraph 2 (1) (b) of Act No. 634 / 1992 Coll., on Consumer Protection. '
4. In Article 3, the following sentence is added at the end of paragraph 1: "This shall also apply to the sponsorship of actions or activities involving several Member States of the European Union or other States constituting the European Economic Area or taking place in several Member States of the European Union or in other States constituting the European Economic Area or achieving cross-border effects by other means."
5. Paragraph 3 (2) reads as follows:
"(2) Advertising of tobacco products shall also mean:
(a) any form of commercial communication the purpose or direct or indirect effect of which is to promote a tobacco product;
(b) free distribution of a tobacco product, the purpose or direct or indirect effect of which is to promote a tobacco product or free distribution which has such direct or indirect effect in connection with the sponsorship referred to in paragraph 1;
(c) advertising which does not refer directly to the tobacco product but uses the trade marks 1a), an emblem or other characteristic feature of the tobacco product, unless otherwise specified. '
6. in Article 3 (4) (a), the words "notice designated" shall be replaced by the words "advertising in periodical prints2), non-periodical publics3), on flyers, posters or other printed matter or in electronic means 10a) determined."
Footnote 10a:
"10a) § 2 (c) of Act No. 480 / 2004 Coll. '.
7. in Article 3 (4) (e):
"(e) publications which are printed and published in third countries, unless they are primarily intended for the internal market of the European Communities."
8. In Paragraph 5 (1), the words "They shall be regarded as advertising 'shall be replaced by the words" These are in particular'.
9. In Article 5 (1) (c), "aid 'is replaced by" aid'.
10. in Article 5 (1) (d), the words "to encourage the prescription, sale, supply or consumption of medicinal products for human use" shall be inserted after the word "meeting."
11. in Article 5a (2), at the end of point (b), comma shall be replaced by a dot and point (c) shall be deleted;
12. in Paragraph 5a (3):
"(3) Paragraph 2 shall not apply to medicinal products for human use used in a vaccination operation approved by the Ministry of Health. ';
13. in Paragraph 5a (5) (b), the words "its common name" are replaced by the words "the normal name of this medicinal product for human use."
14. In Article 5a, the following paragraph 6 is inserted after paragraph 5:
"(6) Advertising of medicinal products for human use for which efficacy has not been assessed in the context of a marketing authorisation procedure 15a) may contain only data on the packaging or package leaflet of such medicinal products for human use under specific legislation15b).
15a) § 24a of Act No. 79 / 1997 Coll., as amended by Act No. 129 / 2003 Coll.
15b) Sections 26c and 26d of Act No. 79 / 1997 Coll., as amended by Act No. 129 / 2003 Coll. Decree No. 288 / 2004 Coll., laying down the details of the marketing authorisation of medicinal products, their changes, extensions, classification of medicinal products for supply, transfer of marketing authorisation, the issue of authorisations for parallel import, submission and design of specific treatment programmes using non-authorised medicinal products for human use, the method of notification and evaluation of adverse effects of the medicinal product, including the need for periodic safety update reports, and the manner and extent of notification of the use of the non-authorised medicinal product (the marketing regulation on medicinal products). '
Paragraphs 6 and 7 shall be renumbered paragraphs 7 and 8.
15. in Article 5a (7) (f), the words "to be issued or represented by experts (for example actors) and" to be deleted and the word "medicines" shall be replaced by "medicinal products for human use."
16. in Paragraph 5a (7), the comma at the end of point (k) shall be replaced by a dot and point (l) shall be deleted;
17. in Paragraph 5a (8):
"(8) Where advertising aimed at the general public is intended as a reminder of a medicinal product for human use, it shall not contain particulars other than the name of the medicinal product for human use as specified in the marketing authorisation or its international non-proprietary name, if any, if such a trade mark exists. ';
18. In Paragraph 5b, the following sentence is added at the end of paragraph 2: "The provisions of this paragraph shall not apply to advertising for medicinal products for human use for which the effectiveness of the marketing authorisation procedure has not been assessed (15a). Paragraph 5a (6) shall apply to the advertising content of the product experts. '
19. In Paragraph 5b, the sentence "The sales agent shall, without undue delay, transmit to the relevant marketing authorisation holder 17a information on the relevant facts which he / she becomes aware of in the course of his / her activity concerning the use of the medicinal product for which he / she carries out the advertising, in particular any undesirable effects reported to him by the persons visited. '
Footnote 17a reads:
"17a) § 52a paragraph 1 (a) of Act No. 79 / 1997 Coll., as amended by Act No. 129 / 2003 Coll. '.
20. Paragraph 5b (5) reads:
"(5) Scope of free entertainment and accommodation
(a) at a meeting attended by experts to promote the prescription, sale, supply or consumption of medicinal products for human use; or
(b) at a meeting of experts for professional or scientific purposes;
be proportionate, having regard to the main purpose of the meeting secondary and not extended to persons other than experts; in that case, the scope of the entertainment and accommodation provided shall not be subject to the prohibition laid down in paragraph 4. ';
21. In Paragraph 5b (7), the first sentence shall be replaced by the sentence "Samples of medicinal products for human use may be provided only exceptionally to persons authorised to prescribe them, in a limited number for a maximum of one calendar year, each sample shall correspond to the smallest packaging of the medicinal product for human use placed on the market and shall bear the inscription" Unsold sample "or" Free sample. "
22. in Paragraph 5b (8):
"(8) Where advertising aimed at professionals is intended as a reminder of a medicinal product for human use, it shall not contain particulars other than the name of the medicinal product for human use as specified in the marketing authorisation or its international non-proprietary name, if any, if any. ';
23. Article 5c, including the title and footnotes 18, 19, 20 and 21, shall be deleted.
24. in § 5d (d), including footnotes 23 and 23a:
"(d) by attaching the food to the characteristics of the prevention, treatment, treatment or cure of human diseases or to such properties as indicate; However, this shall not prevent the presentation of information or recommendations intended exclusively for persons qualified in the field of medicine, nutrition or pharmacy for food for special medical purposes (23); in the case of mineral water, such restrictions shall not prevent the indication that mineral water promotes or facilitates certain vital functions of human organism23a),
23) Decree No. 54 / 2004 Coll., on foodstuffs intended for particular nutritional uses and their method of use.
23a) Article 9 (2) (c) of Council Directive 80 / 777 / EEC of 5 July 1980 on the approximation of the laws of the Member States relating to the exploitation and sale of natural mineral waters. '
25. in § 5d, the following point (e) is added:
"(e) by recommending a food with reference to inspecific clinical studies.";
26. In § 5d, the present text becomes paragraph 1 and the following paragraphs 2 and 3 are added:
"(2) Advertising for dietary supplement 23b) must contain a clear, in the case of printed advertising well-read, text" food supplement. "
(3) Advertising of food for particular nutritional uses (23) must contain a clear, well-readable text in the case of printed advertising, "food for particular nutritional uses."
23b) § 2 (j) of Act No. 110 / 1997 Coll., as amended. '
27. After § 5g, the following § 5h is inserted:
Veterinary medicinal products
The object of advertising aimed at the general public must not be:
(a) veterinary medicinal products which, under the marketing authorisation provided for in special legislation14) may be issued only on medical prescription;
(b) veterinary medicinal products containing narcotic or psychotropic substances (16). "
28. in Article 6, the word "or" shall be added at the end of point (b).
29. in Article 6b (4), "3" is replaced by "4."
30.
Supervision of compliance
(1) The authorities responsible for supervising compliance with this law (hereinafter referred to as the "supervisory authority") are:
(a) Broadcasting Council (28) for advertising in radio and television broadcasting and for sponsoring in radio and television broadcasting,
(b) the State Institute for Drug Control (29) for the advertising of medicinal products for human use and sponsorship in this field, with the exception of the scope referred to in (a);
(c) the Ministry of Health (30) for advertising health care and sponsorship in this field, except for the scope referred to in (a);
(d) State plant health management26a) for advertising on plant protection products, with the exception of the scope referred to in (a);
(e) the Institute for State Control of Veterinary Bioprafts and Medication31) for advertising veterinary medicinal products, except for the scope referred to in (a);
(f) the Office for the Protection of Personal Data for Unsolicited Advertising, disseminated by electronic means 10a) under the Specific Legislation 32),
(g) Regional Trade Offices 32a) in other cases.
(2) In the exercise of supervisory activity, supervisory authorities shall be governed by Part Three of the State Control Act 32b), unless otherwise provided for in that Act. In the course of the inspection, the staff of the supervisory authorities may also record sound and images.
28) Act No 231 / 2001 Coll., on the operation of radio and television broadcasting and amending other laws, as amended.
29) Article 9 of Act No. 79 / 1997 Coll., as amended.
30) § 70 of Act No. 20 / 1966 Coll., as amended.
31) Article 12 of Act No. 79 / 1997 Coll., as amended.
32) Paragraph 10 (1) (a) of Act No. 480 / 2004 Coll.
32a) Act No. 570 / 1991 Coll., on Trade Offices, as amended.
32b) Act No. 552 / 1991 Coll., on State Control, as amended. '
31. In the first sentence of Paragraph 7a (1), the word "processor 'is replaced by the word" contracting authority'; in the second sentence, the word "processor 'is replaced by the word" contracting authority'.
32. in Article 7a (2), the words "and other materials and information relating to such advertising" shall be inserted after the words "advertisements entered."
33.Paragraph 7b (4) is deleted.
34. The following Sections 7c and 7d are inserted after Section 7b:
Specific measures
(1) The supervisory authority may order the removal or termination of advertising which is contrary to the law and specify a reasonable period. The supervisory authority shall be entitled to suspend the spread of misleading advertising for medicinal products for human use if the dissemination could endanger the life or health of persons. No actual loss or other damage caused by such advertising or the fault of the advertiser shall be required for such a procedure; However, this does not constitute an authorisation for the introduction of a prior checking system for advertising proposals prior to its dissemination.
(2) The supervisory authority shall publish the decision given in accordance with paragraph 1 or § 8a in an appropriate manner if, as a result of the further dissemination of advertising, the life or health of persons could be at risk. The supervisory authority shall be entitled to order the contracting authority or the advertising processor to publish within the time limit set for the publication of a corrective declaration on the advertising of medicinal products for human use which has been found to be misleading by a final decision and the removal or termination of which has been final decided in the same communication medium to which such advertising has been disseminated. The costs of the publication of the corrective statement shall be borne by the person to whom the supervisory authority has ordered its publication.
Order fine
(1) The supervisory authority may impose an order fine of up to CZK 50 000 for failure to provide the necessary synergies
(a) to a contracting entity which fails to fulfil an obligation under Article 7a (1), last sentence or Article 7a (2);
(b) a processor who fails to comply with an obligation under Article 7a (3); or
(c) to an operator who fails to fulfil an obligation under Paragraph 7a (4).
(2) The order fines referred to in paragraph 1 may also be imposed repeatedly; the total of the fines imposed must not exceed CZK 200,000.
(3) The revenue from the ordered fine shall be the revenue from the budget from which the activity of the authority which imposed the fine is borne. ';
35. Sections 8 and 8a, including the title, read:
"Administrative offences
(1) A natural person, as a propagator, commits an offence by:
(a) not notify the person who proves the legitimate interest in accordance with Article 6b (2) who is the contracting authority or processor;
(b) disseminate advertising prohibited under Article 2 (1) (a);
(c) does not separate or clearly distinguish advertising distributed together with any other communication from any other communication;
(d) infringes the obligation to distinguish the dissemination of product or service information from that of tobacco product pursuant to Article 3 (3);
(e) infringes the prohibition on the free supply of samples to the general public of tobacco products pursuant to Article 3 (7) or for medicinal products for human use pursuant to Article 5a (4);
(f) disseminate advertising on plant protection products in breach of § 5g;
(g) disseminate to the public advertising of veterinary medicinal products contrary to § 5h;
h) spread advertising on firearms and ammunition contrary to § 6;
(i) disseminate advertising of funeral activities in breach of § 6a (2) or (3);
(j) disseminate unsolicited advertising where such disseminated advertising results in expenditure incurred by the addressee or harasses the addressee; or
(k) infringes the prohibition on advertising based on subthreshold perception.
(2) A natural person as a procuring entity for advertising is guilty of an offence by:
(a) award an advertisement which, pursuant to Article 2 (1) (a) or Article 3 (1), is prohibited or contrary to Article 3 (5);
(b) infringes the conditions laid down for the content of advertising in § 2 (3) or (4), § 2b, 2c, § 3 (6), § 4, § 5 (3), (4) or (5), § 5a (1), (2), (6), (7) or (8), § 5b (2) or § 5d, § 5e (1), § 5f, § 5g (1), § 5h or § 6a (1);
(c) infringes the conditions laid down for comparative advertising set out in Article 2 (2) or Article 2a;
(d) enter an advertisement which is misleading; or
(e) it shall not keep a sample (copy) of any advertising pursuant to Paragraph 7a (1) or lend a copy of the advertising to the supervisory authorities free of charge for the period strictly necessary.
(3) The expert commits an offence by requiring or accepting benefits prohibited under § 5b (4) or contrary to § 5b (5).
(4) The offence referred to in paragraph 1 (a) and paragraph 2 (e) may be fined up to CZK 500 000, the offence referred to in paragraph 3 shall be fined up to CZK 100 000, the offence referred to in paragraph 1 (b) to (j) and paragraphs 2 (a) to (c) shall be fined up to CZK 2 000, the offence referred to in paragraph 1 (k) shall be fined up to CZK 5 000 000 and the offence referred to in paragraph 2 (d) shall be fined up to CZK 10 000 000 000. A fine of up to CZK 5,000 may be imposed in block proceedings for the offence referred to in paragraphs 1 to 3.
(1) A natural person, whether legal or legal, commits an administrative offence by:
(a) not notify the person who proves the legitimate interest in accordance with Article 6b (2) who is the contracting authority or processor;
(b) disseminate advertising prohibited under Article 2 (1) (a);
(c) does not separate or clearly distinguish advertising distributed together with any other communication from any other communication;
(d) infringes the prohibition on advertising based on subliminal perception;
(e) infringes the prohibition of advertising hidden;
(f) disseminate unsolicited advertising where such disseminated advertising results in expenditure incurred by the addressee or harasses the addressee;
(g) infringes the obligation to distinguish the dissemination of product or service information from that of tobacco product pursuant to Article 3 (3);
(h) infringes the prohibition of free supply of samples to the general public for tobacco products pursuant to Article 3 (7) or for medicinal products for human use pursuant to Article 5a (4);
(i) disseminate advertisements for medicinal products for human use targeted at professionals by means of means of communication not intended primarily for such professionals;
(j) infringes the obligations of the commercial agent under § 5b (3);
(k) infringes the prohibition to offer, promise or provide gifts or other benefits pursuant to Paragraph 5b (4);
(l) provide samples of medicinal products for human use contrary to § 5b (7);
(m) infringes the obligation laid down for the dissemination of advertising for infant formulae pursuant to Article 5e (2) or (3);
(n) disseminate advertising of plant protection products contrary to § 5g;
o) spread advertising on firearms and ammunition contrary to § 6;
(p) disseminate advertising of funeral activities contrary to § 6a (2) or (3); or
(q) disseminates to the public advertising of veterinary medicinal products which contravenes § 5h.
(2) A natural person who is a legal or legal person commits an administrative offence by:
(a) it shall not keep a demonstration (copy) of any advertising pursuant to Article 7a (1) or lend a copy of the advertising to the supervisory authorities free of charge for the period strictly necessary;
(b) award an advertisement prohibited under § 2 (1) (a), § 3 (1) or § 6a (3);
(c) infringes the prohibition on advertising based on subliminal perception;
(d) enter an advertisement which is misleading;
(e) infringes the prohibition of advertising hidden;
(f) infringes the conditions laid down for comparative advertising set out in Article 2 (2) or Article 2a;
(g) infringes the conditions laid down for the advertising content in § 2 (3) or (4), § 2b, 2c, § 3 (6), § 4, § 5 (3), (4) or (5), § 5a (1), (2), (6), (7) or (8), § 5b (2) or § 5d, § 5e (1), § 5f, § 5g (1), § 5h or § 6a (1); or
(h) shall not indicate advertising for tobacco by warning pursuant to Article 3 (5).
(3) A natural person, whether legal or in business, commits an administrative offence by:
(a) it shall process advertising prohibited or contrary to § 5g (2) (a), § 3 (1) or § 6a (3);
(b) infringes the prohibition of advertising hidden;
(c) infringes the prohibition on advertising based on subliminal perception;
(d) to process an advertisement which is misleading;
(e) infringes the conditions for comparative advertising laid down in Article 2 (2) or Article 2a;
(f) infringes the conditions for the advertising content laid down in § 2 (3) or (4), § 2b, 2c, § 3 (6), § 4, § 5 (3), § 5a (1), (2), (3), 5, 6 or 7, § 5b (2) or (8), § 5d, § 5e (1), § 5f, § 5g (1), § 5h or § 6a (1); or
(g) shall not mark advertising on a tobacco product by warning pursuant to Article 3 (5).
(4) A natural person, whether legal or legal, commits an administrative offence by:
(a) infringes the prohibition to offer, promise or provide gifts or other benefits pursuant to Article 5b (4);
Sign in for notes, favorites and notifications
Regulation Information
| Citation | Act No. 25 / 2006 Coll., amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended, and Act No. 132 / 2003 Coll., amending Act No. 40 / 1995 Coll., on the regulation of advertising and amending and supplementing Act No. 468 / 1991 Coll., on the operation of radio and television broadcasting, as amended |
|---|---|
| Regulation Type | - |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 26.01.2006 |
|---|---|
| Effective from | 26.01.2006 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
Comments 0