Subject: MRM Clinical Research Seminars

From: "[email-masked]" <[email-masked]>
Date: 13 Oct 2008 00:31:00 -0400

To send this email to a friend click here

SEMINARS, E-LEARNING PROGRAMS, and 140-HR CRA Certificate Program

Volume Discounts Available
Seminars provide the Information on Latest Legislation and FDA Guidelines

Seminar
Title: Coordinating a Clinical Trial - 2 Days

Next Date & Location:
October 16th and 17th, 2008 in Coral Springs, FL

Click Here to View Agenda/Course Description

COST:
$995.00

Seminar
Title: Drug/Biologic GCP and an Overview of Monitoring - 2 Days

Next Date & Location:
October 30th and October 31st, 2008 in Coral Springs, FL

Click Here to View Agenda/Course Description

COST:
$995.00

Seminar
Title: Medical Device GCP and an Overview of Monitoring - 2 Days

Next Date & Location:
December 4th and 5th, 2008 in Coral Springs, FL

Click Here to View Agenda/Course Description

COST:
$995.00

Seminar Title: Writing Professional Monitoring Reports - 1 Day

Next Date & Location:
January 14th, 2009 in Coral Springs, FL

Click Here to View Agenda/Course Description

COST:
$595.00

Seminar
Title: Advanced Quality Monitoring - 3 Days

Next Date & Location:
January 15th, 16th, and 17th, 2009 in Coral Springs, FL

Click Here to View Agenda/Course Description

COST:
$1195.00

New! Comprehensive training, Pre and Post Testing, Training Management

CRC Online Training Program accompanied by a textbook and workbook.

COST: $295.00

Investigator Online Training Program accompanied by a textbook.

COST: $445.00

Complying with the HIPAA Privacy Rule in Research accompanied by a textbook.

COST: $245.00

Kind
Regards,

Medical Research Management, Inc.

www.CRA-Training.com

(877) 633-3322

Please
visit our website for details:

WWW.CRA-TRAINING.COM

Or
Call : 877-633-3322

Ask about our onsite seminars for your corporation. We will bring all the necessary training materials to you. Call 877-633-3322 for more information.

140-HR CRA Certificate Program

Part 1: Online with text-book and regulatory CD-ROM provided.

Part 2: Two weeks hands on training with competency and regulatory exams.

Fundamentals of Clinical Research, an interactive program providing online and
classroom training for the clinical research professional, begins with the
history of legislation and regulations that govern clinical research and an
overview of drug, biologic, and device development. Course participants develop
a thorough knowledge base of Good Clinical Practices and International
Conference of Harmonization guidelines (E6, E2A), gaining a solid understanding
of clinical trial development and management.

The Part 2 classroom training focuses on developing a
systematic approach to monitoring, conflict resolution, and problem solving. The
participants monitor 6 study subjects and 3 regulatory binders across two study
types. Writing effective and professional monitoring reports is also addressed.
During the review and discussion of GCP issues, the instructor highlights the
differences between device and drug/biologic studies.

Payment Schedule:

$1,995 required for Part 1; this provides
the applicant with access to the online course. Course textbook and materials
sent via express mail;

$1,500 is due on, or prior to the Part 2 “Training” starting date.

To remove your name from our mailing list. click here. Questions or Comments? Email us at [email-masked] or call 877-633-3322.