Events
Areas of Interest
Overview
The International SharePoint Conference
23, April 2012 - 25, April 2012
Interest Area(s)
Development and implementation of SharePoint applications for Life Sciences
Overview
SharePoint conference that covers IT Professionals, Developers, End Users and Business tracks. The event is structured to provide combined knowledge, ideas and needs covering the IT infrastructure, development, implementation, Information Worker / End User and the Business requirements (CEO’s, project managers, business analysts, Information architects and key decision makers involved in SharePoint projects).
Attending? Find us exhibiting at the ARX stand or email at info@gxpi.com to arrange a meeting.
ShareFEST 2012
19, April 2012 - 20, April 2012
Interest Area(s)
Use of SharePoint in Life Sciences
Overview
ShareFEST is the premier SharePoint Conference for Life Sciences. ShareFEST 2012 will be held on April 19-20, in Philadelphia, PA. The conference attracts several hundred attendees from pharmaceutical companies, device manufacturers, biotechs and service providers from around the world. The first conference was held in 2010 which attracted attendees from more than 120 different life science organizations from around the world.
Attending the conference and want to arrange a meeting with us? Call us or send a request to info@gxpi.com
DIA Regulatory Information Management Conference
24, April 2012 - 25, April 2012
Interest Area(s)
Clinical Research,Project Management,IT/Validation,Regulatory Affairs,Medical Writing
Overview
Regulatory Information Management
Regulatory departments are continually being asked to do more with less. In addition, regulatory authorities are increasing the scrutiny related to patient safety and compliance with approved application information. As regulatory departments are challenged to develop global regulatory strategies, coupled with the corporate desire to launch in global markets early, the need to understand the regulatory requirements for filing, timelines, what products are approved in which markets is becoming a critical regulatory need for both industry and regulators. Effective regulatory information management processes and tools are needed to ensure the organization remains compliant with its product registrations.
This conference will feature a business focused track and a technology focused track. The Business Track will provide the opportunity to interact and share experiences related to processes for obtaining and managing regul…
ISPE UK Affiliate - GAMP Forum - April 2012
26, April 2012
Interest Area(s)
GAMP
Overview
Include information on the aims and objectives of the day, the main topics to be covered, the session chairman and any keynote speakers.
This free of charge event, sponsored by CTG, provides a valuable networking and information exchange opportunity for pharmaceutical professionals in the UK. The event focusses on Computerized Systems Validation discussions and the agenda includes cloud computing, a look at the revisions of the Testing and Laboratory Systems Good Practice Guides, testing systems for blood services, Agile methodologies, and promotional practices, as well as the regular GAMP and regulatory updates.
ISPE UK Affiliate - GAMP Forum - October 2012
02, October 2012
Interest Area(s)
GAMP
Overview
Include information on the aims and objectives of the day, the main topics to be covered, the session chairman and any keynote speakers.
This free of charge event, sponsored by AstraZeneca, provides a valuable networking and information exchange opportunity for pharmaceutical professionals in the UK. The event focusses on Computerized Systems Validation discussions and the agenda includes global compliance experiences, a risk management workshop and information on a risk-based approach to infrastructure qualification as well as the regulatory updates.
12th Conference on European Electronic Document Management/ EDM
30, November 2011 - 02, December 2011
Interest Area(s)
Clinical Data Management/ eClinical,CMC,Clinical Research,Document Management/ eSubmissions,IT/Validation,Medical Writing,Strategic Planning,Quality Assurance/Quality Control,Regulatory Affairs,Clinical Safety/Pharmacovigilance
Overview
Overview:
For the past few decades, as we moved from paper-based content to electronic files, we have kept a clear distinction between documents and data, and the context in which this content was used. Data was managed in structured databases, analysed, then transferred manually, and documents were recreated over and over again and stored in eDM systems.
Today this separation is slowly disappearing as new technologies, such as XML, bring documents, data and other forms of information together in one melting point. This evolution is welcome and opens new perspectives in areas such as collaboration, reuse, review, analysis and records management. It also creates new challenges and pharmaceutical professionals will need to revise their view and practices and gradually move from traditional data and document management to information and content management.
DIA has always been in the forefront of new ideas and technologies and will once more offer a p…
ISPE GAMP - Improve Productivity with Risk-Based Systems Validation Conference
14, November 2011 - 15, November 2011
Interest Area(s)
GAMP
Overview
Many companies are not sure what the regulatory impact of hot new technologies may be, and as a result sometimes find that they have wasted time and money on ineffective initiatives.
Attending this session will help you understand the implications such new technologies have, and you’ll see approaches that can help you to better manage your data. Join Regulators and Industry experts during round table discussions on virtualisation, cloud computing and outsourcing.
For more information and to register your interest please click on the link below
ISPE GAMP - Improve Productivity with Risk-Based Systems Validation Conference
PharmaCloud World Europe 2011
08, November 2011 - 09, November 2011
Interest Area(s)
Clinical Data Mangagement/eClinical, CMC, Clinical Research, Document Management/eSubmissions, IT/Validation, Medical Writing, Strategic Planning, Quality Assurance/Quality Control, Regulatory Affairs
Overview
Pharma Cloud World Europe is Europe's leading cloud computing conference for senior pharmaceutical & biotech executives.
This conference will discuss the opportunities and challenges, strategies and operational implementation of cloud computing for the pharmaceutical industry.
Pharma Cloud World Europe is a multi-faceted event consisting of:
- A two day conference
- A exhibition area
- Speed networking
- Interactive panel discussions
- Roundtable brainstorms
- Live debates
Validation in the PharmaCloud
GxPi Talk 17:15 on Tuesday 8th November
- Will QA help or hinder progress towards cloud computing for Pharma R&D?
- "Qualifying" a cloud-based environment versus "Validating" an application.
- Assessing and mitigating, the risks of hosting GxP-Regulated applications in the cloud.
