A Guide to Pharmacovigilance Audits in the USA | Agenda Bookshop Skip to content
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Please note that books with a 10-20 working days delivery time will not arrive before Christmas.
A01=Heather Murphy
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Age Group_Uncategorized
Author_Heather Murphy
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Category1=Non-Fiction
Category=MF
Category=MMG
Category=MQP
Category=PN
COP=Switzerland
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Language_English
PA=Not yet available
Price_€100 and above
PS=Forthcoming
softlaunch

A Guide to Pharmacovigilance Audits in the USA

English

By (author): Heather Murphy

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.

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Current price €126.34
Original price €132.99
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A01=Heather MurphyAge Group_UncategorizedAuthor_Heather Murphyautomatic-updateCategory1=Non-FictionCategory=MFCategory=MMGCategory=MQPCategory=PNCOP=SwitzerlandDelivery_Pre-orderLanguage_EnglishPA=Not yet availablePrice_€100 and abovePS=Forthcomingsoftlaunch

Will deliver when available. Publication date 18 Dec 2024

Product Details
  • Dimensions: 155 x 235mm
  • Publication Date: 18 Dec 2024
  • Publisher: Springer International Publishing AG
  • Publication City/Country: Switzerland
  • Language: English
  • ISBN13: 9783031735950

About Heather Murphy

Heather Murphy is a expert Pharmacovigilance (PV) professional with her focus in Pharmacovigilance Operations and PV Audits. For over 20 years she has established PV and reengineered PV departments for companies in various stages of development within the pharmacovigilance industry. As a result of her hands on experiences she has successfully developed PV systems for small-large size companies in preparation for US and global product launch. PV Operations activities have ranged from the strategic to tactical with extensive experience in PV inspections including the FDA EMA PMDA AIFA Health Canada MHRA ANSM BfArM and Swiss Medic. Current PV audit activities include audits for/of preinspection preparation routine and for cause vendor qualification REMS business partner contract resource organizations (CROs) specialty pharmacies warehouse vendors supply vendors and distribution vendors. She is a Certified Quality Auditor (CQA) through the American Society of Quality obtained a MBA from Suffolk University in Boston MA a Bachelor of Science in Nursing (BScN) from Dalhousie University in Nova Scotia Canada and an RN from the Prince Edward Island School of Nursing in P.E.I Canada.  

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