zum Inhalt wechseln
The challenge of CMC regulatory compliance for biopharmaceuticals and other biologics Titelvorschau
SchließenTitelvorschau
Prüfung…

The challenge of CMC regulatory compliance for biopharmaceuticals and other biologics

Verfasser/in: J Geigert
Verlag: New York, NY : Springer, ©2013.
Ausgabe/Format   E-Book : Dokument : Englisch : 2nd edAlle Ausgaben und Formate anzeigen
Datenbank:WorldCat
Zusammenfassung:
An effective CMC regulatory compliance strategy for biologics and biopharmaceuticals can seem like a mystery. Through means of this 2nd edition, this no longer needs to occur. A great deal of thanks goes to two regulatory authorities - the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA), who provide through their respective websites, an abundance of guidance, especially in  Weiterlesen…
Bewertung:

(noch nicht bewertet) 0 mit Rezensionen - Verfassen Sie als Erste eine Rezension.

Themen
Ähnliche Titel

 

Online anzeigen

Links zu diesem Titel

Exemplar ausleihen

&AllPage.SpinnerRetrieving; Suche nach Bibliotheken, die diesen Titel besitzen ...

Details

Gattung/Form: Electronic books
Medientyp: Dokument, Internetquelle
Dokumenttyp: Internet-Ressource, Computer-Datei
Alle Autoren: J Geigert
ISBN: 9781461469162 1461469163
OCLC-Nummer: 843402928
Beschreibung: 1 online resource.
Inhalt: Complexity of biologic CMC regulation --
Biologics are not chemical drugs --
An effective CMC strategy is possible --
Challenge of adventitious agent control --
Source materials for biologics --
Manufacture of the biologic API --
The biologic final product process --
Complex process-related impurities --
Molecular structural analysis --
Functional activity (Potency) --
Setting specifications and expiry dates --
Demonstrating product comparability --
CMC-focused regulatory meetings.
Verfasserangabe: John Geigert.
Weitere Informationen:

Abstract:

In its new edition, this book reviews the challenges facing quality assurance and control (QA/QC) in today's biopharmaceutical environment, putting into perspective the need for a graded approach to  Weiterlesen…

Rezensionen

Nutzer-Rezensionen
Suche nach GoodReads-Rezensionen
Suche nach DOGObooks-Rezensionen…

Tags

Tragen Sie als Erste Tags ein.
Anfrage bestätigen

Sie haben diesen Titel bereits angefordert. Wenn Sie trotzdem fortfahren möchten, klicken Sie auf OK.

Verlinkung


<http://www.worldcat.org/oclc/843402928>
library:oclcnum"843402928"
library:placeOfPublication
library:placeOfPublication
owl:sameAs<info:oclcnum/843402928>
rdf:typeschema:Book
rdfs:seeAlso
schema:about
schema:about
schema:about
<http://id.worldcat.org/fast/1060114>
rdf:typeschema:Intangible
schema:name"Pharmaceutical biotechnology industry--Law and legislation"
schema:about
rdf:typeschema:Intangible
schema:name"Technology, Pharmaceutical--legislation & jurisprudence."
schema:about
rdf:typeschema:Intangible
schema:name"Technology, Pharmaceutical--standards."
schema:about
<http://id.worldcat.org/fast/1060109>
rdf:typeschema:Intangible
schema:name"Pharmaceutical biotechnology--Quality control"
schema:about
schema:about
schema:about
rdf:typeschema:Intangible
schema:name"MEDICAL / Pharmacology"
schema:about
schema:about
schema:author
schema:bookEdition"2nd ed."
schema:bookFormatschema:EBook
schema:copyrightYear"2013"
schema:datePublished"2013"
schema:description"An effective CMC regulatory compliance strategy for biologics and biopharmaceuticals can seem like a mystery. Through means of this 2nd edition, this no longer needs to occur. A great deal of thanks goes to two regulatory authorities - the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA), who provide through their respective websites, an abundance of guidance, especially in the last several years. So much has changed since the 1st edition of this book was published in 2004. There are now additional manufacturing processes for producing commercial biopharmaceuticals - transgenic plant cell cultures and transgenic animals. In addition to commercial recombinant proteins and monoclonal antibodies, there are now commercial cell-based medicines (cellular therapy) and DNA-based medicines (gene therapy). Biosimilars are now on the marketplace in Europe, and under review for commercial approval in the USA. Vaccine manufacturing has resurged due to the concerns of potentially pandemic mutated animal influenzas (e.g., swine flu, bird flu). Strategic international regulatory guidances have been adopted that are driving the entire pharmaceutical industry, including biopharmaceuticals, to a higher standard of performance, including Quality by Design (QbD), Quality Risk Management (QRM) and Pharmaceutical Quality Systems (PQS). The vast majority of the over 600 regulatory references listed in this book were either issued or updated since the release of the 1st edition. All of these changes are the reason this updated edition includes not only biopharmaceuticals but also other biologics (e.g., live virus vaccines, human plasma-derived proteins, cell-based medicines, natural-sourced proteins) that have CMC regulatory compliance concerns and challenges in common with the genetically-engineered biologics (i.e., the biopharmaceuticals). About The Author John Geigert is President of BioPharmaceutical Quality Solutions, which specializes in providing CMC regulatory strategy consulting for the biopharmaceutical and biologic industry. Dr. Geigert has over 35 years of CMC industrial experience and leadership in the biopharmaceutical industry. Dr. Geigert has served on the PDA Board of Directors, co-chaired the PDA Biotech Advisory Board and served as an expert member of the USP Biotechnology Committee. Dr. Geigert has written extensively for the Regulatory Affairs Professional Society (RAPS) Focus (What Senior Management Needs to Know About CMC Regulatory Compliance for Biotech Products (Aug-Nov 2009, 4-part series) and Demystifying CMC Regulatory Strategy (Sept 2011-Mar 2012, 4-part series))."
schema:exampleOfWork<http://worldcat.org/entity/work/id/673009>
schema:inLanguage"en"
schema:name"The challenge of CMC regulatory compliance for biopharmaceuticals and other biologics"
schema:publisher
schema:url<http://dx.doi.org/10.1007/978-1-4614-6916-2>
schema:url<http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=580248>
schema:url<http://site.ebrary.com/id/10699675>
schema:workExample
schema:workExample

Content-negotiable representations

Fenster schließen

Bitte in WorldCat einloggen 

Sie haben kein Konto? Sie können sehr einfach ein kostenloses Konto anlegen,.