Drug Regulatry affair: Bone of Pharmaceutical Research and development

  • Lubna Azmi Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute, Lucknow-226 001, Uttar Pradesh
  • Ila Shukla Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute, Lucknow-226 001, Uttar Pradesh
  • Padam Kant Department of Chemistry, Lucknow University, Lucknow
  • Ch. V. Rao Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute, Lucknow-226 001, Uttar Pradesh
Keywords: Dyslipidemia, type 2 diabetes, lipid profile, Benghazi, Libya

Abstract

Regulatory Affairs is a relatively new profession which has developed from the wish of governments to defend public health, by scheming the safety and efficacy of products in areas including pharmaceuticals , medical devices, pesticides, veterinary medicines, agrochemicals, cosmetics and complementary drugs. The companies accountable for the testing, produce, discovery and marketing of these products also want to make sure that they supply products that are safe and create a worthwhile input to public health and welfare. Most companies, whether they are main multinational pharmaceutical companies or small, innovative biotechnology companies, have specialist segment of Regulatory Affairs professionals.

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Published
2018-10-31
How to Cite
1.
Azmi L, Shukla I, Kant P, Rao C. Drug Regulatry affair: Bone of Pharmaceutical Research and development. IJPP [Internet]. 31Oct.2018 [cited 18Mar.2019];8(5):39-4. Available from: https://ssjournals.com/index.php/ijpp/article/view/4922
Section
Review Article