Global
CompliancePanel
Knowledge, a Way Forward
2-day In-person Seminar:
Clinical Research for Cardiovascular Pharmaceuticals:
Ensuring Compliance of Traditional and New Cardiovascular Medications
Price
Washington, DC
Price:
May 26th & 27th, 2016
9:00 AM to 6:00 PM
Charlene M. Jett
President3R's Management Consulting and Therapeutics Inc
Charlene M. Jett lives in Vandalia Illinois about 70
miles east of St. Louis. She is a scientist, clinical researcher, consultant,
adventurer, volunteer, daughter of Charles W. and Sybel Harre.
Charlene is well educated and has a Master's of Science in
Management (1990) from Lake Forest Graduate School of
Management, Lake Forest Illinois, a Master's of Science in Biology
(1980) from Northeastern Illinois University, Chicago, Illinois and a
Bachelor's of Science in Physiology (1972) from University of Illinois,
Champaign-Urbana, Illinois.
Overview:
Understanding basic clinical research requires excellent people and
project management skills, and very good scientic writing and
organization skills. Also paramount is gathering necessary information to
manage the statistical analysis and data management of all the many
clinical studies. The clinical development plans must be laid by
experienced leaders and project managers. The clinical plan includes the
budgets and timeline necessary to properly research the drug and
advance it through all the testing necessary to achieve approval by FDA.
The various phases of drug development (Phases I-IV) are necessary for
most new chemical entities. Protocols are required for all clinical tests
and this usually starts with a literature review, establishing key efcacy
and safety parameters and determining proper sample size.
$1,295.00
(Seminar for One Delegate)
Register now and save $200. (Early Bird)
**Please note the registration will be closed 2 days
(48 Hours) prior to the date of the seminar.
2-day In-person Seminar
Global
CompliancePanel
Why should you attend:
Areas Covered in the Session:
This seminar should be attended to ensure the proper
Basic Clinical Research,
compliance and development of traditional and new
Scientic Methodology,
cardiovascular medications. Failure to attend could
result in poorly managed clinical trials, wasted nancial
resources and liability based law suits. The
Regulations and Law
Basic Project Management
development of well-designed clinical trials and rigorous
monitoring is required. From the literature review to the
last appendix a complete understanding of regulations
FDA and IRBs
Who will benet:
Clinical Research Associates
pertaining to clinical research and monitoring a welldesigned protocol is necessary. All project managers
Scientists
know that the critical path thru clinical research is
Nurses
extremely tightly regulated and fraught with pitfalls.
Financing by the sponsor/developer of the drug is
highly scrutinized for value and good management.
Pharmacists
Pharmacologists
Monitoring according to Good Clinical Practice
guidelines is required to determine evaluable patients.
The more mistakes that are made the higher the cost.
Doctors
Medical Directors
AGENDA:
Day One
Day Two
Lecture 1: Pharmaceutical Companies and Planning
Lecture 1: Protocols and Monitoring
Lecture 2: Drug Development and FDA Regulations
Lecture 2: Medical and Statistical (Evaluable patients)
Lecture 3: Clinical Plans and Budgets
Lecture 3: Reviews and Meetings
Lecture 4: Discussion and Q and A
Lecture 4: Discussion and Q and A
2-day In-person Seminar
Global
CompliancePanel
What You will get
Group Participation
10%
2 Attendees to get offer
20%
3 to 6 Attendees to get offer
25%
30%
Learning Objectives
Participation certificates
Interactive sessions with the US expert
Post event email assistance to your queries.
Special price on future purchase of web
7 to 10 Attendees to get offer
10+ Attendees to get offer
Payment Option
based trainings.
Credit Card: Use the Link to make Payment by
Visa/Master/American Express card click on the
register now link
Special price on future consulting or expertise
services.
Check: Kindly make the check payable to
NetZealous DBA GlobalCompliancePanel and
mailed to 161 Mission Falls Lane, Suite 216,
GlobalCompliancePanel.
Fremont, CA 94539, USA
PO: Please drop an email to
[email protected] or call the
Special price on future seminars by
Seminar Kit includes presentation handout,
our toll free +1-800-447-9407 for the invoice and
ID card, brochure, trainings catalog, notepad
you may fax the PO to 302 288 6884
and pen.
Wire Transfer: Please drop an email to
[email protected] or call our
toll free +1-800-447-9407 for the wire transfer
Networking with industry's top notch professionals
information
Contact Information: Event Coordinator
161 Mission Falls Lane, Suite 216,
Kindly get in touch with us for any help or
information.
Fremont, CA 94539, USA
Look forward to meeting you at the seminar
NetZealous LLC, DBA GlobalComplianePanel
Toll free: +1-800-447-9407
Fax: 302 288 6884
Email:
[email protected]www.globalcompliancepanel.com
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