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Related Experiment Video

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Radiosynthesis, Quality Control, and Small Animal Positron Emission Tomography Imaging of 68Ga-Labelled Nano Molecules
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Current veterinary regulations and way ahead.

Shubham J Suryawanshi1, Siddharth Jain1, Rakesh K Sharma2

  • 1Amity Institute of Pharmacy, Amity University, Noida, Uttar Pradesh 201303, India.

Research in Veterinary Science
|November 28, 2023
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Summary
This summary is machine-generated.

This review compares global veterinary medicine regulations (2016-2023). Key findings show a lack of specific legislation for zoonotic diseases, drug stockpiling, and dedicated pharmacopoeias across most nations, highlighting areas for regulatory improvement.

Keywords:
PharmacologyStockpilingVeterinary medicine regulationVeterinary pharmacopoeiaVeterinary pharmacovigilanceZoonotic disease

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Area of Science:

  • Veterinary Medicine
  • Regulatory Science
  • Comparative Policy Analysis

Background:

  • Global veterinary medicine regulations vary significantly across nations.
  • Existing frameworks may not adequately address emerging threats like zoonotic diseases or ensure drug supply chain resilience.
  • Standardization and oversight in veterinary medical devices and pharmacovigilance are inconsistent.

Purpose of the Study:

  • To conduct a comparative systematic review of veterinary medicine regulations from 2016 to 2023.
  • To identify gaps and inconsistencies in regulatory frameworks across key global regions (USA, EU, UK, Japan, Australia, India).
  • To provide recommendations for enhancing the quality and safety of veterinary medicines.

Main Methods:

  • Systematic review of legislative acts and directives related to veterinary medicine.
  • Comparative analysis of drug approval processes and regulatory oversight.
  • Assessment of regulations concerning zoonotic diseases, pharmaceutical stockpiling, pharmacopoeias, medical devices, and pharmacovigilance.

Main Results:

  • Significant absence of specific regulations for zoonotic diseases and pharmaceutical stockpiling in most reviewed countries.
  • Lack of dedicated veterinary pharmacopoeias for standardization of raw materials and formulations globally.
  • Inconsistent regulation of veterinary medical devices, with only the USA and Australia having specific frameworks.
  • Limited establishment of dedicated veterinary pharmacovigilance centers, with Australia being the sole country identified.

Conclusions:

  • There is a critical need to integrate specific legislation for zoonotic diseases and strategic pharmaceutical stockpiling into global regulatory frameworks.
  • Development of dedicated veterinary pharmacopoeias is essential for ensuring the quality and standardization of veterinary drugs.
  • Implementing robust regulations for veterinary medical devices and establishing dedicated pharmacovigilance centers are crucial for improving animal health and safety.
  • Harmonizing regulations and addressing identified gaps will enhance the overall quality, safety, and efficacy of veterinary medicines worldwide.