Analytical Science Essay Example | Topics and Well Written Essays - 750 words

Analytical Science - Essay Example Others are counterfeit drugs and outright fake ones. The need of the drug regulations was necessary so as to guarantee that there was efficiency safety, and superiority of drugs in addition to exactness and the correctness of the drug information that are available to the society (Habet, 32) . The work was not aimed to rank the countries under the study against any criterion. Rather, the aim was to synthesize their experiences and later draws conclusions on generic from countries that were participating and others get to learn from them. There was a systematic study was done of drug regulations and its surroundings across countries and there was shed a new illumination on the state of affairs of the country. these was so since there needed to provide a new perspective about the constraints it was facing, and also provide the options on the way to advance the means the method was to function. The structures of drug regulations that exist today that is the drug regulatory, laws, evalua tion boards, quality control laboratories, informational centers have evolved over with time. In this process the scope of the regulatory powers and legislative had gradually expanded, in regards to both the increasing complexity of the increasingly sophisticated pharmaceutical sector, and the perceived requirements of the society (Foroutan, 69). In other countries, the enactment of the comprehensive drugs regulations was as a result of the crisis-led change, when the society demands led then the adoption of laws that are restrictive so as to provide greater safe guards to the society. The drug regulation body is a society policy that response to the perceived requirements and the problems of the society. Consequently, the laws need to be upgraded to keep up the pace of the changes and the new challenges in the surroundings (Pika 24). The laws ought to be protective to the society from dubious and harmful drugs and practices. They need to be inclusive adequate to cover up all areas of pharmaceutical activities in the country. These include the herbal or homeopathic drugs they ought to be legal mandates that are imposed on the importation of drugs. The essay laid down the conclusions on generic from the weakness and strengths of different types and then identifies the features that affect the performance of the regulation of drugs. The government acted as the guardian of controlling the private powers in the public purposes. These have ensured the efficacy, safety and the quality of drugs that are available to the society was the main aim of the drug regulation. If the goals based on regulatory were to be achieved, then the appropriate structures were to be invented and the correct activities carried out acquire the desired goals. The rapid HPLC method for Analysis Temperature (Â °C) Old Formulation Methylprednisolone Conc. (ppm) New Formulation Methylprednisolone Conc. (ppm) 30 45.21 Â ± 3 46.1 Â ± 2.100 40 41.34 Â ± 4.2 40.45 Â ± 4.123 50 40 Â ± 3.54 39 Â ± 5 60 35.67 Â ± 6 38.987Â ± 4 70 37 Â ± 2.456 37.34 Â ± 3.654 80 21.567 Â ± 3.234 36.321 Â ± 1.567 90 23 Â ± 5 37.23 Â ± 5.012 Â   Â   Â   Temperature (Â °C) Formulation 1 Methylprednisolon