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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR

Cell Line Development and Engineering

Cell Line Development and Engineering

23-25 April 2018
RAI, Amsterdam

Cell Line Development & Engineering 2018 event will be held 23-25 April 2018 in the RAI Amsterdam joining the largest Bioprocessing event in Europe  BPI Europe.

With 900+ attendees, 275+ companies and over 70 sessions showcasing new data and technologies, this year is one not to be missed! Premier industry-led cell line development and engineering event 3 days dedicated to cutting edge science, technologies and strategies:
Day One: Monoclonality & Complex Molecules
Day Two: Cell Line & Host Cell Engineering
Day Three: Automation & Manufacturability Assessment

SIGN UP NOW AND SAVE MORE: https://lifesciences.knect365.com/cell-line-congress/?vip_code=CQ3568EBR

Contact:
T: +44 (0) 20 3377 3279
E: LS.Registrations@Knect365.com 

phone +44 (0) 20 3377 3279
email LS.Registrations@Knect365.com
web bit.ly/2opwE08
email RAI, Amsterdam
 
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White Papers

PhlexEarchive: The Right Solution for Electronic Archiving of TMF Content

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Many sponsor organizations have already recognized the value of moving from paper to electronic Trial Master Files (eTMFs). But few sponsors have taken a more holistic approach to the TMF lifecycle and looked at the entire process from study start-up through archiving of the TMF in electronic format, also known as e-archiving. The recurring value of managing, tracking, maintaining and accessing electronic files should not stop at the point of archiving. All of the challenges of managing an active paper TMF carry through to a paper archive. All of the benefits of an electronic TMF also carry through to the electronic archive. As companies look to move their compliance assets to secure, long-term storage, it is important to consider ongoing compliance requirements, security, accessibility, efficiency and costs of archiving TMF content in a digital format.
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News and Press Releases

PCI Clinical Services Announces New Facility Dedicated to Clinical Trial Returns

Philadelphia, USA October 15, 2018. Leading international pharmaceutical outsourcing services provider PCI Clinical Services (PCI) has announced the completion of a dedicated Returns Management facility at its Clinical Services Center of Excellence at Bridgend, UK. PCI provides a full service Returns Management service for clients, providing visibility and accountability in returning investigational drug product from investigational sites at the conclusion of a clinical study. Returning and reconciling Investigational Medicinal Product (IMP) on completion of a study is a critical part of a Clinical trial and can require complex reverse logistics. Trial outcomes can be impacted if Returns are not processed efficiently and precisely.
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