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About StudyProtocol

StudyProtocol is a software platform from StudyProtocol - Protocol Labs that assists researchers in designing and managing clinical trial protocols. It provides customizable templates, collaboration tools, and compliance tracking so users can efficiently create and monitor their study protocols. The platform is designed to facilitate communication among research teams and ensure adherence to regulatory standards. Key capabilities: customizable templates collaboration tools compliance tracking version control user permissions Best for: researchers and clinical trial managers that need to create and oversee clinical study protocols.

StudyProtocol Details

Vendor
StudyProtocol - Protocol Labs
Year Launched
Location
Protocol Labs Headquarters: 153 Townsend Street, Suite 800, San Francisco, CA 94107, United States
Deployment
Training Options
demo, account manager, community
Countries Served
All Countries
Languages
English, Spanish, French, German, Italian, Portuguese, Chinese, Japanese, Russian, Korean, Dutch, Arabic
Users
Principal Investigator, Study Coordinator, Research Assistant, Data Manager, Clinical Research Associate, Regulatory Affairs Specialist, Biostatistician, Investigational Pharmacist, Ethics Committee Member, Study Sponsor
Industries Served
Healthcare, Life Sciences, Pharmaceutical
Tags
Clinical Trial Management, Study Protocol, Protocol Labs

StudyProtocol's In-App Market Place

Does StudyProtocol have an in-app market place?

Yes

How many Mini-Apps in the marketplace?

10

Mini Apps

1. Electronic Data Capture (EDC) Integration - Allows seamless integration with popular EDC platforms to streamline data collection and analysis for clinical trials.

2. Patient Recruitment Toolkit - Provides tools and resources for efficiently recruiting participants for clinical trials

including targeted marketing campaigns and patient screening tools.

3. Regulatory Compliance Tracker - Automates the tracking of regulatory requirements and deadlines to ensure compliance throughout the entire trial process.

4. Investigator Site Management Tool - Helps manage and coordinate activities at investigator sites

including training tracking

site performance monitoring

and document management.

5. Adverse Event Reporting Module - Facilitates the collection and reporting of adverse events during the course of a clinical trial

to ensure timely and accurate reporting to regulatory authorities.

Pricing Options

Free trial
Free version
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Accepted Payment Currencies

USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (CHF), CNY (¥), SEK (kr), NZD (NZ$), KRW (₩), INR (₹), SGD (S$), HKD (HK$), NOK (kr), MXN (MX$), DKK (kr), PLN (zł), TRY (₺), RUB (₽), ZAR (R), BRL (R$), MYR (RM), IDR (Rp), SAR (﷼), AED (د.إ), THB (฿), PHP (₱), CLP (CLP$), COP (COL$), ILS (₪), TWD (NT$), ARS ($)

Pros & Cons

  • Allows for efficient and systematic design of clinical trial protocols
  • Helps ensure important details and considerations are not overlooked
  • Streamlines the protocol approval process
  • Facilitates collaboration among team members involved in the protocol development
  • Provides a framework for ensuring protocol adherence and consistency
  • Helps improve the overall quality and rigor of clinical trials.
  • Limited customization options for study protocols
  • Interface can be confusing and not user-friendly
  • Steep learning curve for new users
  • Lack of mobile optimization for on-the-go access
  • Limited integrations with other clinical trial management tools
  • Subscription pricing model may be expensive for smaller research teams

StudyProtocol's Support Options

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