Regulatory Compilation Report



Price: $495.00

Fulfillment: Electronic files will be fulfilled once full payment is received by CenterWatch. You will receive an email with an attached PDF upon order completion if purchased during normal business hours Monday-Friday, between 8 a.m. and 3:30 p.m. EST. Otherwise, orders will be fulfilled the next business day. Purchasers must provide an active email address during checkout registration.

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The fourth report in the Compilation Report Series, the Regulatory Compilation Report, focuses on GCP and methods used to ensure compliance with regulatory requirements that safeguard data integrity and human subject protection in clinical trials. Topics range from ‘Right to Try’ laws to the Physician Payment Sunshine Act.

Conveniently provided in a PDF format, this report may be used in round-table discussions, strategic business and marketing reports, conference presentations or organizational meetings.

Recommended for:

  • Professionals at pharma, biotech, medical device, CROs, sites and service providers involved with clinical trials.

Additional resources:

  • The CenterWatch Monthly newsletter features proprietary data and original market research, drug development analysis, and clinical study lead opportunities in each issue.
  • Market Research Intelligence Services (MRIS) provides custom quantitative and qualitative projects assisting companies in developing, executing and evaluating strategies and practices within the life sciences and clinical research industry.
  • Benchmark Report Series are data-driven reports compiled from original surveys conducted among clinical research professionals and results analyzed by CenterWatch across a range of topics—Global Site Relationships, Career and Salary, and Financial and Operating Practices.
Product Details


Publication date:
October 2017

Multi-user licenses:
Contact Sales at,
(866) 219-3440

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