Related Experiment Video
Updated: Jan 17, 2026

Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform
Published on: August 17, 2022
How to implement pre-emptive pharmacogenetic testing in the acute hospital setting
John Henry McDermott1,2, Ali Shoaib3, Jessica Keen1,2
1Division of Evolution, Infection and Genomics, School of Biological Sciences, University of Manchester, Manchester, UK.
Implementing a pharmacogenomics program requires careful planning. This guide outlines essential elements, including team and resource needs, for establishing a sustainable pharmacogenomics initiative.
Area of Science:
- Pharmacogenomics
- Genetics
- Personalized Medicine
Background:
- Hospitals are increasingly adopting pharmacogenomics programs.
- Successful implementation requires strategic planning and resource allocation.
- Lessons learned from global pharmacogenomic programs offer valuable insights.
Purpose of the Study:
- To outline the essential components for establishing a sustainable hospital-based pharmacogenomics program.
- To identify key interdependencies, opportunities, and challenges in pharmacogenomics program implementation.
- To provide a framework for healthcare institutions seeking to introduce pharmacogenomics services.
Main Methods:
- Review of successful global pharmacogenomic programs.
- Identification of critical elements for program sustainability.
- Analysis of interdependencies, opportunities, and challenges.
Main Results:
- Key considerations include team composition, resource allocation, and infrastructure.
- Successful programs demonstrate strong interdisciplinary collaboration.
- Challenges involve integration into clinical workflows and data management.
Conclusions:
- Establishing a pharmacogenomics program is feasible with strategic planning.
- A dedicated team and adequate resources are crucial for sustainability.
- Addressing interdependencies and challenges proactively ensures program success.
More Related Videos
05:53Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
Published on: June 21, 2018
08:46Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Related Concept Videos
Dosage Regimens: Partial Pharmacokinetic Parameters
Analysis of Population Pharmacokinetic Data
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Measurement of Bioavailability: Pharmacodynamic Methods
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...