Quality Assessment of Investigational Medicinal Products in COVID-19 Clinical Trials: One Year of Activity at the Clinical Trials Office

Bibliographic Details
Title: Quality Assessment of Investigational Medicinal Products in COVID-19 Clinical Trials: One Year of Activity at the Clinical Trials Office
Authors: Diego Alejandro Dri, Giulia Praticò, Elisa Gaucci, Carlotta Marianecci, Donatella Gramaglia
Source: Pharmaceuticals, Vol 14, Iss 12, p 1321 (2021)
Publisher Information: MDPI AG, 2021.
Publication Year: 2021
Collection: LCC:Medicine
LCC:Pharmacy and materia medica
Subject Terms: clinical trials, COVID-19, investigational medicinal products, quality, regulatory, Medicine, Pharmacy and materia medica, RS1-441
More Details: One year after the spread of the pandemic, we analyzed the assessment results of the quality documentation submitted to the Clinical Trials Office of the Italian Medicines Agency as part of the request for authorization of clinical trials with a COVID-19 indication. In this article, we report the classification of the documentation type, an overview of the assessment results, and the related issues focusing on the most frequently detected ones. Relevant data regarding the Investigational Medicinal Products (IMPs) tested in COVID-19 clinical trials and their quality profiles are provided in the perspective of increasing transparency and availability of information. Some criticalities that have been exacerbated by the management of clinical trials during the emergency period are highlighted. Results confirm that IMPs tested in authorized COVID-19 clinical trials are developed in agreement with the same legal requirements for quality, safety, and efficacy as for any other medicinal product in the European Union (EU). The same strong regulatory framework applies, and there is no lowering in the safety profile due to the pandemic; authorized IMPs meet the highest standards of quality. The regulatory network should capitalize on lessons learned from the emergency setting. Some take-home messages are provided that could support the regulatory framework to expand its boundaries by innovating and evolving even though remaining strong and effective.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1424-8247
Relation: https://www.mdpi.com/1424-8247/14/12/1321; https://doaj.org/toc/1424-8247
DOI: 10.3390/ph14121321
Access URL: https://doaj.org/article/d9bd60dac5ec4ac19e790fbef0a40e0a
Accession Number: edsdoj.9bd60dac5ec4ac19e790fbef0a40e0a
Database: Directory of Open Access Journals
More Details
ISSN:14248247
DOI:10.3390/ph14121321
Published in:Pharmaceuticals
Language:English