Abstract
The common denominator between the commercial companies, wanting to optimise profits from existing and novel pharmaceuticals, and the national regulatory licensing authorities, is that both want to make safe, new drugs available to the patient population. For example, the EEC Rules which govern medicaments (1) state that the primary purpose of the comunity rules relating to the medicinal products is to safeguard public health whilst at the same time ensuring that the development of the pharmaceutical industry and trade in medicinal products will not be hindered.
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References
The Rules Governing the Medicaments in the European Community. Commission of the European Communities, July 1984
Council Directive 65/65/EEC. Official Journal of the European Communities, No 22, 9.2. 1965: 369–365
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Council Directive 83/570/EEC No L332/1, 26.10.1983
Guidelines for the Clinical Evaluation of Radiopharmaceutical Drugs. HHS (FDA) 81–320: 3.
Guidelines for the Clinical Evaluation of Radiopharmaceutical Drugs. HHS (FDA) 81–320: 4.
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© 1987 Martinus Nijhoff Publishers, Dordrecht
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Neirinckx, R.D. (1987). Relationships Between Industry, Hospitals and Authorities. In: Kristensen, K., Nørbygaard, E. (eds) Safety and Efficacy of Radiopharmaceuticals 1987. Developments in Nuclear Medicine, vol 14. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-3375-0_23
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DOI: https://doi.org/10.1007/978-94-009-3375-0_23
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-010-8016-3
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