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

support@globalcompliancepanel.com 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

support@globalcompliancepanel.com 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: support@globalcompliancepanel.com

www.globalcompliancepanel.com

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