Managing Offshore Outsourced Software Development

Sesstion Type: Recorded Webinar
Speaker: Jan Villumsen, Specialist Quality, NNE Pharmaplan A/S

Gain specific guidance on how to run offshore outsourced projects. Learn what makes these projects different, what to be aware of, and how to organize an offshore outsourced setup.

Who Should Attend

Project managers and line managers responsible for offshoring or outsourcing development activities.

Agenda Topics

Introduction
Overview of offshore outsourcing setups
Selecting the project model
How distance matters
Running multi-site projects
IT infrastructure
Contract development
Communicating across cultures
Conclusion
Question and answer

Take Back to Your Job

Insight on how to run multi-site projects as well as contract development
How to cope with distance through clear communication, purpose and agenda for trips
Understanding issues of well-defined processes, cultural differences, and IT infrastructure

Speaker Biography:

NNE Pharmaplan A/S has software development facilities in China, Sweden, France, USA and Denmark. Villumsen undertakes technical management in computer compliance and offshore outsourcing. Previously he worked in consulting engineering for an independent non-profit R&D organization, with manufacturers of data and telecommunication equipment, and for the pharmaceutical industry. As engineering manager at Tellabs Denmark A/S, he headed network management development and established a development team in Delhi, India. Villumsen received his M.Sc.E.E. in 1986 from the Technical University of Denmark.

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Previously held webinars are available as recorded sessions, which you can view at your convenience. Registration orders are processed within two business days, after which participants will receive an e-mail confirmation with a link to the Recorded Webinar. After receiving the link to the Recorded Webinar, you have 15 days to view it.

What are CPIP^SM Recorded Webinars?

CPIP^SM Recorded Webinars are a group of Recorded Webinarswas developed to help individuals in preparation for the Certified Pharmaceutical Industry Professional^SM (CPIP^SM) examination..

The Certified Pharmaceutical Industry Professional^SM (CPIP^SM) credential recognizes “change agents” as the necessary ingredient to foster industry innovation and enhance drug product quality. The credential establishes a global competency standard for industry professionals, and candidates are assessed through demonstrated education, experience, and a rigorous examination. Completion of any of these seminars does not guarantee successful completion of the CPIP certification exam, and these seminars do not include every subject to the depth of what will be covered on the CPIP exam.

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