Regulatory of Personalized Medicine
The FDA is already started to take initiatives to integrate personalized medicine into their regulatory policies. They developed a report in October 2013 entitled Paving the Way for Personalized Medicine FDAs role in a New Era of Medical Product Development in which they outlined steps they would have to take to integrate genetic and biomarker information for clinical use and drug development. They determined that they would have to develop specific regulatory science standards, research methods, reference material and other tools in order to incorporate personalized medicine into their current regulatory practices. For example, they are working on a genomic reference library for regulatory agencies to compare and test the validity of different sequencing platforms in an effort to uphold reliability.
Related Conference of Regulatory of Personalized Medicine
May 16-17, 2025
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&
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Regulatory of Personalized Medicine Conference Speakers
Recommended Sessions
- Metabolomics in Personalized Medicine
- Biomarkers Personalized Medicine
- Developed of Personalized Medicine
- Economics of Personalized Medicine
- Ethics of Personalized Medicine
- Molecular Diagnostics in Personalized Medicine
- Non- genomics Personalized Medicine
- Personalized Biological Therapies
- Personalized in Health Care
- Personalized Management of Cardio Vascular
- Personalized Management of Genetic Disorders
- Personalized Management of Immune Disorders
- Personalized Management Of Infectious Diseases
- Personalized Management of Neurological Disorder
- Personalized Management of Psychiatric Disorders
- Personalized Management of Pulmonary Disoders
- Personalized Non-Pharmacological Therapies
- Personalized Vaccines
- Pharmacogenetic in Personalized Medicine
- Pharmacogenomics in Personalized Medicine
- Pharmacoproteomics in Personalized Medicine
- Regulatory of Personalized Medicine
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