The debate on this Bill has been comparatively short. Questions were raised, some of a specific nature and some of a more general nature to which I think I ought to refer in my reply.
One of the specific questions raised came from Deputy Sweetman in which he made a complaint about conditions which certain manufacturers benefiting by the protection impose as far as the distribution of their goods is concerned. There is, as Deputies know, protective duty in force in respect of textile goods but there is also provision whereby a certain amount of these goods is permitted to be imported free of duty under licence. In many cases there is also attaching to the import free of duty of these goods a condition that the person importing these goods must purchase a certain proportion of similar goods from Irish factories.
The complaint made by Deputy Sweetman, so far as I could understand it, was that in some cases these factories which benefited from protection insisted that all their output should be purchased by the consuming public, by wholesalers or retailers, through one agent. I should like to assure him that there is certainly no condition of such a nature attaching to any import licences issued by my Department. If there is any restriction imposed by any manufacturer in the case of a specific item I should like to hear from him what that case is and if he gives me the necessary particulars I shall have it investigated. Even though he did not identify any manufacturer or any commodity yesterday, I did, in the time intervening between yesterday and today, try to find out whether there was any specific case in which my Department had a complaint and I could find none. Therefore, even though Deputy Sweetman is not here, I shall invite him to give me particulars of his complaint and I can assure him I shall have it investigated.
The other specific matter raised was in connection with the duty imposed last year on medicinal tablets. The duty in this case, as in most other cases, was imposed for the purpose of protecting a worthwhile Irish industry and, as in all cases, there was no prior consultation with other interests. I think the practice is well established and well understood that in the case of the imposition of a new duty there is no consultation with other interests for obvious reasons, the most obvious being to avoid attempts to stock up in advance of the imposition of the duties. The complaint was made that there should have been prior consultation with medical opinion or with pharmacist opinion but that was not done in this case either.
In cases where duties are imposed and advice of a technical or professional nature is necessary for my officials, that advice is usually available from official sources. In the case of the medicinal tablets the advice sought was from the Department of Health who have qualified medical men and qualified pharmacists on their staff who are able to give whatever advice is necessary.
The same procedure was adopted in this case as was adopted by the last Government when they imposed a duty on injection solutions. The same advice was sought and the same action was taken on that occasion. That was in 1955. There were fears expressed then from medical and pharmacist sources that there might be some hardship or that there might be some difficulty about people not getting the type of injection solution to which they were used or for which they had a preference. These fears were expressed by medical authorities and by pharmacists. In practice, however, the fears proved to be groundless. Ever since that duty was imposed no difficulties have come to the knowledge of my Department.
Similarly, in the case of the duty imposed on medicinal tablets there were fears expressed originally, largely by distributors of medical preparations. These distributors were, in the main, people who were agents of foreign companies who used export these tablets to this country. Fears were also expressed by Deputies by way of Questions put on the Order paper and supplementary questions. On these occasions I was able to assure the Deputies that no hardship was envisaged. In the event, I understand no problem that was not capable of being overcome has arisen.
One of the objections raised at that time was that the prices of Irish tablets would be higher than those of corresponding imported tablets. At the time of the imposition of the duty, the firm that made application for the duty gave an undertaking that they would not increase their prices beyond the current levels and they were able to show to the satisfaction of my Department that their prices ex-factory corresponded to the British ex-factory prices. If there had been increases in the prices of the Irish commodity over and above a reasonable amount beyond factory prices, it is something that is capable of being remedied by the purchaser himself.
I also assured the House that, as regards tablets that were not being manufactured or were not to be manufactured by Irish companies, there would be no difficulty about procuring the necessary licences for the importation of these tablets duty free. That, in fact, has been the case in general. No problems have arisen that have not been capable of being surmounted and there have been no protests from medical sources in particular. In recent months there seem to have been no complaints expressed about difficulties.
Deputy Dillon raised the problem of a person who had a preference for a particular type of tablet even though there might have been no difference— and certainly that would have been generally known—between the components of the home-manufactured tablets and the imported tablets. Nevertheless, that person did express a preference for a particular imported tablet and believed that the imported tablet was better for the ailment from which he suffered. I should like to assure Deputy Dillon that even such cases have been taken into account. There is no import duty whatever on lots of tablets up to 100. Therefore, if anybody has a preference for one tablet rather than another and finds that tablet is not being manufactured in this country, even though a similar tablet is, that person can go to his usual channel of supply and procure in lots of 100 as often as he likes, the particular tablet for which he has a preference. I think that answers any fears Deputy Dillon might have in that respect.
He also raised the question of testing and of standards. There is a system well-established in the Department of Health whereby the pharmacist staff carry out inspection of premises in which tablets are made in Ireland. The principal manufacturer here has attained a very high standard. His factory is regularly inspected and in fact he has invited medical representatives to visit the factory and they have done so from time to time. In each case, I am given to understand, they were fully satisfied with the standards maintained, with the quality of the products and with the hygiene of the premises. There are standards formally laid down in the British Pharmacopoeia and in the British Pharmaceutical Codex for medical preparations. These formulae apply here and it is an offence to sell any tablets that are identified in the Pharmacopoeia or in the Codex which do not comply with these formulae; so we can be satisfied that, in general, the question of testing and of standards is well safeguarded in this country.
Deputy Dr. Browne raised the question as to whether the drug list issued by the Department of Health of medical preparations for use by authorities under its control or under its aegis will in future contain Irish-made drugs and tablets. I have not any control over the content of these drug lists but I am informed in general that the imposition of this duty makes no difference to the practice which has obtained hitherto. In particular, I should like to comment on the point made by Deputy Russell that patients who go to dispensaries which are central dispensaries for the distribution of drugs complain that since the imposition of this duty they have not been able to get the particular tablets which they feel are best for them and which they have been accustomed to take. Again, I am told that no change has been made in the administration of the Health Acts in the dispensing and supply of particular drugs in dispensaries throughout in the country. I am also assured by the Department of Health that in so far as there is a need for a particular type of tablet which requires to be imported even though it is made here, the local health authority usually makes provision to have it available to the public.