The CRC's Guide To Coordinating Clinical Research
Description:
Topics covered include:
*Developing standard operating procedures (SOPs)
*Recruiting and retaining study subjects
*Understanding the informed consent process
*Working with protocols and case report forms
*Recognizing adverse events
*Preparing for audits
The CRC's Guide to Coordinating Clinical Research is recommended for:
*Novice and experienced CRCs
*Professionals interested in getting involved with clinical research at the investigative site level
*Investigative site staff
Best prices to buy, sell, or rent ISBN 9781930624467
Frequently Asked Questions about The CRC's Guide To Coordinating Clinical Research
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