Evidence map›Paper›PMID 35789167›Full record

ArticleScientific reports2022

Development and Delphi validation of instrument for the preparation of a GMP audit of a cosmetic contract manufacturer in the UAE.

Ammar Abdulrahman Jairoun, Sabaa Saleh Al-Hemyari, Moyad Shahwan, Faris El-Dahiyat, Justyna Bisgwa, Shazia Jamshed, Hanady Yousef Shourrab

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Ammar Abdulrahman JairounHealth and Safety Department, Dubai Municipality, Dubai, United Arab Emirates. Dr_ammar_91_@hotmail.com.ORCID 0000-0002-4471-0878
Sabaa Saleh Al-HemyariSchool of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, Malaysia.
Moyad ShahwanDepartment of Clinical Sciences, College of Pharmacy and Health Sciences, Ajman University, Ajman, United Arab Emirates. moyad76@hotmail.com.
Faris El-DahiyatClinical Pharmacy Program, College of Pharmacy, Al Ain University, Al Ain, United Arab Emirates.
Justyna Bisgwa *, Opole, Poland.
Shazia JamshedDepartment of Clinical Pharmacy and Practice, Faculty of Pharmacy, Universiti Sultan Zainal Abidin, 21300, Kuala Terengganu, Malaysia.
Hanady Yousef ShourrabDrug Department, Ministry of Health and Prevention, Dubai, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outsourcing is rapidly increasing in the cosmetic industry. When cosmetic manufacturing activities are outsourced, product quality control and assurance procedures are important to guarantee the safety of the final products. One method to ensure the compliance of potential contract manufacturers with Good Manufacturing Practices (GMP) is auditing. Auditing can be confirmed by using GMP questionnaires. The current study aims to develop an effective instrument, in the form of a questionnaire, and to validate its content using the Delphi method. A modified Delphi method used an expert panel to develop a questionnaire-based audit preparation instrument. In the Delphi questionnaire round, 50 experts from cosmeceutical industries, relevant authorities, and universities assessed the content validity of the audit preparation instrument. The Delphi questionnaire round targeted 70 experts from the cosmetics industry; 50 completed the questionnaire, giving a response rate of 71.4%. Their agreement level on the quality of the instrument items ranged between 56 and 96%. Of the 52 items, 47 (90.4%) met the predefined criterion for an agreement rate of at least 75%. The proposed audit preparation instrument demonstrated good content validity, and the expert panel participating in the Delphi questionnaire round made a few minor suggestions for modifications. The modified Delphi method used for the content validation of the instrument proved to be suitable. However, based on the panel's feedback, additional research is needed to ensure the maximum applicability and practicality of the instrument.

Indexed as

CosmeticsResearch DesignSurveys and QuestionnairesCosmetics

Identifiers

PMID35789167
PMCPMC9253126

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.