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A guide to pharmacovigilance audits in the USA

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	A guide to pharmacovigilance audits in the USAby Heather Murphy.
作者:	Murphy, Heather.
出版者:	Cham :Springer Nature Switzerland :2024.
面頁冊數:	xii, 146 p. :ill., digital ;24 cm.
Contained By:	Springer Nature eBook
標題:	PharmacovigilanceAuditing.United States
電子資源:	https://doi.org/10.1007/978-3-031-73596-7
ISBN:	9783031735967$q(electronic bk.)

A guide to pharmacovigilance audits in the USA
Murphy, Heather.

A guide to pharmacovigilance audits in the USA[electronic resource] /by Heather Murphy. - Cham :Springer Nature Switzerland :2024. - xii, 146 p. :ill., digital ;24 cm.

Chapter 1 Introduction -- Chapter 2 Audit Types -- Chapter 3 PV Audit Preparation -- Chapter 4 PV Audit Conduct -- Chapter 5 Audit Report -- Chapter 6 Dos and Don'ts of a successful audit.

Pharmacovigilance Audits are an important and growing requirement for Pharmaceutical/BioTech companies. A niche skillset combined with an understanding of audit principles and pharmacovigilance operational and regulatory knowledge are required to effectively conduct these audits This book provides practical guidance to auditors as to what questions to ask, what information to look for, and what documents to request to ensure the auditee Pharmacovigilance System is compliant with regulations, contractual requirements, and industry best practice. The scope is limited to the requirements based on the US Food and Drug Administration (FDA) Regulations. This is an ideal book for auditors and auditees who want to obtain practical PV auditing skills to use within the BioTechnology/Pharmaceutical Industry in the USA.

ISBN: 9783031735967$q(electronic bk.)

Standard No.: 10.1007/978-3-031-73596-7doiSubjects--Topical Terms:

984872
Pharmacovigilance
--Auditing.--United States

LC Class. No.: RM302.5

Dewey Class. No.: 615.7042

A guide to pharmacovigilance audits in the USA
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