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Training
LifeCyte, Inc. offers custom tailored FDA regulations compliance and training for the biopharmaceutical and medical device industries. Our expert trainers combine technical backgrounds and extensive experience to provide in-depth regulatory training featuring case-based learning and instructive personal accounts relating to implementation of regulations. Topics include: GLP, GTP, GCP and GMP regulations, offered in an efficient 2-day format. Onsite training is available to address your specific annual operator training needs. A new course, A-Z of European Regulatory Requirements, will be offered in Q3 2009.
Effective GxP Training
Save Your 2009 Date Now!
| January 22 & 23 |
Memphis, TN - GTP |
| March 5 & 6 |
Raleigh, NC |
| April 2 & 3 |
Boston, MA |
| May 14 & 15 |
Grand Rapids, MI |
| June 18 & 19 |
San Diego, CA |
| Q3 2009 |
Houston/Kansas City/Phoenix |
| Q4 2009 |
Baltimore/Seattle/San Francisco |
Rates per Attendee |
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Early-bird |
Group (3+) |
Early/Group |
Standard |
$1,790 |
$1,590 |
$1,520 |
$1,350 |
Academic/Non-profit |
$1,590 |
$1,390 |
$1,350 |
$1,180 |
For Onsite Training options, please call 1-877-531-8003 |
Registration Form
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Benefits of LifeCyte Training
Top Quality
Expert trainers in appropriate regulatory compliance specialties bring real-life experience to the courses
Custom Tailored
Regulations discussed in a way that is relevant to attendees’ scopes of business and unique requirements
Excellent Value
Regional seminars reduce client travel costs and allow for less time away from work
Effective Training
Sessions are engaging and even fun |
