1. About CenterWatch
Founded in 1994, CenterWatch is a trusted source and global
destination of clinical trials information for both professionals and
patients.
CenterWatch provides a wide variety of information services
including grant leads for investigative sites; business
development leads for contract service providers; postings of
career opportunities; listings of clinical trials actively seeking
patients; advertising and promotional opportunities; and
proprietary business analysis and data about the global clinical
trials industry.
As a pioneer in publishing clinical trials information,
CenterWatch was the first web site to publish detailed
information about clinical trials that could be freely accessed by
patients and their advocates. Today, we have the largest online
database of actively recruiting, industry-sponsored clinical trials.

2. CenterWatch
www.centerwatch.com
The global source for clinical trials information: offering news, analysis, study grants,
career opportunities, and trial listings to professionals and patients
Since 1994, we have provided proprietary information about clinical trials
through a variety of newsletters, books, databases, and information services
including:
The CenterWatch Monthly Clinical Trials Listing Service™
Newsletter (CTLS)
Research Practitioner Patient Notification Service
CWWeekly Research Center Profile Pages
CenterWatch News Online JobWatch
Drugs in Clinical Trials Database TrialWatch / Grant Notification
Service

3. Market Drug Periodicals
Intelligence Information and
Services Business News
Site / Vendor
Identification
Training
CenterWatch Guides
Patient
Enrollment
Services (CTLS)
SOPs
Patient Career
Education Services

4. Clinical Trials Listing Service™
http://www.centerwatch.com/clinical-trials/listings/
As one of the first web sites to publish clinical trials actively seeking study
volunteers, CenterWatch continues to be a leading resource for patients
interested in clinical trial participation receiving more than one million
visitors annually to our listings.
When companies post a trial on our Clinical Trials Listing Service™, now
the largest online database with more than 80,000 industry-funded global
clinical trials, this targeted population has direct access to these listings via
a range of distribution channels including: email messaging programs,
email alerts for new trial postings, social media efforts, top search engine
rankings, RSS Feeds, and collaborative relationships with health
associations and other non-profit organizations.

5. Collaborations Health
with Non-Profit Associations
Organizations CTRCs
Patient
Notification
Service Clinical Trials Link
Listing Service Exchanges
Social
Media
RSS
Content Feeds
SEO
License

6. Grant Notification/Site Identification Services
TrialWatch for Sites
TrialWatch for Sites
TrialWatch for sites is a complimentary grant notification service designed to help research centers easily connect
with sponsors and CROs seeking qualified investigators for upcoming trials. Sites complete a brief online profile that
is stored in a database and then matched against grant requests from sponsors and CROs. When a match is found,
the site information is forwarded to the requesting company for consideration. Site profiles can be completed at
www.centerwatch.com/trialwatch_signup.
TrialWatch for Sponsors and CROs
TrialWatch for Sponsors and CROs is a complimentary site identification service that helps companies quickly and
effectively identify active and qualified investigative sites worldwide to conduct upcoming and active phase I through
phase IV clinical trials. Confidential requests can be submitted online at www.centerwatch.com/clinical-
trials/trialwatch .
Research Center Profile Pages
Research Center Profile Pages, located on www.centerwatch.com , are an easy and cost-effective way for sites to
showcase detailed information online about their site offerings and expertise to secure clinical research grants and
contracts, increase their site’s exposure and reach a captive and targeted audience. Profile Pages are completely
customizable and can include images, video presentations, links to company documents, trial listings and more.

7. CenterWatch Monthly:
In-depth Analysis
Periodicals
CW Weekly: CW News Online:
News & Practical Real-time Ongoing
Insights Industry Coverage
and Updates

8. Periodicals and Business News
The CenterWatch Monthly
The CenterWatch Monthly, our flagship publication, is a premier industry resource
providing in-depth, authoritative business coverage for the clinical trials community,
including unparalleled competitive intelligence and grant opportunities and the most
detailed drug pipeline analysis in the industry—all in one comprehensive publication
featuring original CenterWatch data.
CWWeekly
CWWeekly is a leading news source providing expanded analysis on the week’s top
business and financial headlines and trends. Other features include: market intelligence,
patient recruitment tips, drug intelligence and grant opportunities.
CenterWatch News Online
CenterWatch News Online, located on http://www.centerwatch.com/news‐online/ , is a
dynamic and easy-to-navigate online service featuring real-time objective news reports
covering timely stories and emerging trends in the global clinical research industry.
Features include: breaking news and top headlines as selected by the CenterWatch
editorial staff, news beats featuring relevant content on various industry segments and
proprietary CenterWatch data and original, hard-hitting articles on topics of the day.

9. CenterWatch Training Guides
CenterWatch’s training guide series offers effective and practical tools for
those interested in clinical research as well as seasoned professionals
seeking to better understand their roles and improve the management of their
clinical trials operations in a safe and ethical manner.
• A Guide to Patient Recruitment and Retention
• Becoming a Successful Clinical Research Investigator
• Protecting Study Volunteers in Research (CE credits)
• The CRA’s Guide to Monitoring Clinical Research
• The CRC’s Guide to Coordinating Clinical Research
• Global Regulatory Systems: A Strategic Primer for Biopharmaceutical
Product Development and Registration

10. Regulatory Compliance
Standard Operating Procedures for the Conduct of Clinical Research
This SOP was developed to help clinical research sites meet the challenge of maintaining rigorous
standards in a world of diminishing resources. This template has been expanded to include more
procedures to assess study feasibility, recruit subjects and ensure regulatory compliance and is based on
the Code of Federal Regulations and GCP Consolidated Guidelines.
Policies and Standard Operating Procedures for the Institutional Review Board
This SOP is an easy way for IRBs to document policies and procedures that reflect their organization’s
philosophies, standards and innovations while continuing to comply with federal regulations. This SOP
template is based on the Code of Federal Regulations, guidance and ICH/GCP Consolidated Guideline
and the Association for the Accreditation of Human Research Protection Program’s (AAHRPP) standards
for human subject protection.
Standard Operating Procedures for Good Clinical Practice by Sponsors of Clinical Trials
This SOP was created to help pharmaceutical and biotechnology companies maintain the quality
performance and ethical conduct of clinical trials while adhering to U.S. federal regulations. This template
contains 30 procedures addressing all Good Clinical Practice requirements and is based on FDA
regulations and ICH guidelines.
Standard Operating Procedures for Good Clinical Practice by Sponsors of Medical Device Clinical
Trials
This SOP provides detailed SOPs to address specific requirements for medical device research practices
to adhere to a discrete set of FDA regulations and guidance. Organizations that sponsor clinical research
on new medical devices must implement procedures that comply with both Good Clinical Practice
guidelines and federal regulations.

11. Thank you. We look forward to working with you.
Please contact Kevin Swecker with any questions.
Kevin.Swecker@centerwatch.com or 617‐948‐5125