Research and Technology Development Sample Clauses
Research and Technology Development. (1) The Parties acknowledge that innovative technological solutions are integral to the success of the FSP and to enable Australia’s sovereign operational and sustainment capability for the Future Submarine.
(2) To this end, the Parties shall coordinate and collaborate where appropriate on research and development activities, particularly on most recent developments and technical breakthroughs in the naval domain.
(3) Such research and development activities shall be conducted under the instruments referred to in paragraph 4 of this Article.
(4) The Parties shall revise, when necessary, the existing Agreement between the Government of Australia and the Government of the Republic of France Concerning Collaboration on Defence Research and Technology, which entered into force 17 December 1990, and may revise existing, or conclude new, subsidiary administrative arrangements for the purposes of the FSP.
Research and Technology Development. The so-called Clinical Trials Directive of 2001 (Directive 2001/20/EC) provides regulative and administrative provisions relating to implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. The term “good clinical practice” refers to a set of internationally recognised ethical and scientific quality requirements which must be observed for designing, conducting, recording and reporting clinical trials that involve the participation of human subjects in the European Union’s Member States (Art. 1.2). A subsequent Directive (Directive 2005/28/EC) lays down principles and more detailed guidelines for good clinical practice. Here, a number of basic principles are set out to be followed by every trial that falls within the scope of the Clinical Trial Directive (Art. 2), as follows: The rights, safety and wellbeing of trial subjects shall prevail over the interests of science and society. Each individual involved in conducting a trial shall be qualified by education, training, and experience to perform his tasks. Clinical trials shall be scientifically sound and guided by ethical principles in all their aspects. The necessary procedures to secure the quality of every aspect of the trials shall be complied with.
Research and Technology Development. The so-called Clinical Trials Directive of 2001 (Directive 2001/20/EC) provides regulatory and administrative provisions relating to implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. The term “good clinical practice” refers to a set of internationally recognised ethical and scientific quality requirements which must be observed for designing, conducting, recording and reporting