Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Data Validation01:03

Data Validation

Data validation is an essential part of a comprehensive assessment. Validation is confirming or verifying and opening the door to gathering more assessment data as it clarifies vague or unclear data. The process of checking and verifying the collected information is called data validation. The primary purpose of data validation is to ensure data is as free from error, bias, and misinterpretation as possible.
Nursing assessment guides are generally based on holistic models rather than medical...
Data Validation01:15

Data Validation

Method validation is a crucial process in analytical chemistry designed to confirm that a given method consistently produces reliable and high-quality results. This process is essential when a method is applied to different sample matrices or when procedural modifications are made, ensuring that the results meet acceptable standards across various applications.
Key parameters for method validation include:
Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions01:15

Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions

PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Pharmaceutical Alternatives: Excipients and Impurities-Related Therapeutic Nonequivalence01:19

Pharmaceutical Alternatives: Excipients and Impurities-Related Therapeutic Nonequivalence

Pharmaceutical products contain more than just the active drug; they also contain various excipients such as binders, solubilizers, stabilizers, preservatives, and other elements. In some cases, impurities or contaminants might be present. Traditionally, quality control in pharmaceuticals has primarily focused on the analysis of the active drug, often overlooking the impact of these additional components. The recent issue with heparin contamination by over-sulfated chondroitin sulfate, a...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Severe asthma and remission prospects in Europe (SHARP): insights from a multicentre observational study based on the European Severe Asthma Registry.

The Lancet. Respiratory medicine·2026
Same author

Reprocessing of single-use medical devices in cardiology: a systematic literature review of safety and performance characteristics applied to cardiac electrophysiology.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology·2026
Same author

[Innovative medical devices in France: A descriptive study based on public healthcare databases].

Annales pharmaceutiques francaises·2025
Same author

[Gastrointestinal hemorrhage due to a probable warfarin/oseltamivir drug interaction: A case report].

La Revue de medecine interne·2025
Same author

Comparing three natural language processing methods for the automatic identification of epilepsy patients from French clinical notes.

Epilepsia·2025
Same author

Factors associated with medication adherence trajectory among patients treated with oral anticancer drugs: a multicentre cohort study.

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer·2025

Related Experiment Video

Updated: Jul 14, 2026

Failure of Cleaning Verification in Pharmaceutical Industry Due to Uncleanliness of Stainless Steel Surface
07:00

Failure of Cleaning Verification in Pharmaceutical Industry Due to Uncleanliness of Stainless Steel Surface

Published on: August 11, 2017

Impact of pharmacy validation in a computerized physician order entry context.

Candice Estellat1, Isabelle Colombet, Sarah Vautier

  • 1DEpartement d'Informatique Hospitalière, Hôpital Européen Georges Pompidou, 20-40 rue Leblanc, 75908 Paris cedex 15, France.

International Journal for Quality in Health Care : Journal of the International Society for Quality in Health Care
|June 30, 2007
PubMed
Summary

Pharmacy validation of computerized physician order entry (CPOE) showed a moderate impact on reducing prescribing errors. CPOE system improvements are needed for pharmacists to focus on critical interventions.

Related Experiment Videos

Last Updated: Jul 14, 2026

Failure of Cleaning Verification in Pharmaceutical Industry Due to Uncleanliness of Stainless Steel Surface
07:00

Failure of Cleaning Verification in Pharmaceutical Industry Due to Uncleanliness of Stainless Steel Surface

Published on: August 11, 2017

Area of Science:

  • Health Informatics
  • Clinical Pharmacy
  • Patient Safety

Background:

  • Computerized physician order entry (CPOE) systems aim to reduce prescribing errors.
  • Pharmacy validation acts as a secondary error-checking mechanism.
  • The combined impact of CPOE and pharmacy validation on error reduction has not been previously assessed.

Purpose of the Study:

  • To evaluate pharmacist interventions during CPOE prescription validation.
  • To determine the effect of these interventions on the prescribing process.
  • To assess the contribution of CPOE to identified prescribing errors.

Main Methods:

  • Prospective study in a tertiary care university hospital over five days.
  • All medication orders reviewed by pharmacists using CPOE.
  • Analysis of pharmacy alerts, prescription modifications, and error attribution to CPOE.

Main Results:

  • 11% of order lines (399) triggered pharmacy alerts.
  • 26% of alerts directed to prescribers resulted in prescription modification.
  • 17% of potential prescribing errors were deemed life-threatening; 49% were attributed to CPOE.

Conclusions:

  • Pharmacy validation offers a moderate short-term reduction in potential prescribing errors.
  • CPOE system enhancements are crucial for optimizing pharmacist interventions.
  • Improving CPOE can enable pharmacists to focus on more significant prescribing issues.