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features
design
support

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Write a Review

Description

ClinChoice excels in overseeing international regulatory information by leveraging advanced technology, a comprehensive grasp of both global and local regulations, and exceptional data management techniques. By harnessing its regulatory affairs and technological expertise, ClinChoice aids organizations in effectively handling their regulatory data. Our team of consultants offers essential data maintenance assistance within regulatory information management system (RIMS) software, facilitating timely application submissions, approvals, and renewals while enhancing operational efficiency and monitoring. We support the management and oversight of the drug registration process, enabling pharmaceutical and medical device manufacturers to maintain visibility and track all regulatory details. With our guidance, organizations can formulate both immediate and long-term strategies that ensure compliance with submission deadlines, all while minimizing disruption to their everyday operations, ultimately contributing to a smoother regulatory journey. This strategic partnership empowers companies to navigate the complexities of compliance with greater confidence and agility.

Description

Document management and teamwork are streamlined with myClin, which serves as an interactive and dynamic eTMF solution. You can swiftly upload and share research documents through your secure and centralized myClin channels, facilitating immediate access that speeds up the distribution of essential study updates and training information. With oversight built into the process, our "File it" feature allows you to monitor who has reviewed and comprehended your study materials. This feature not only serves as a record of effective study execution but also tracks training activities such as views, filings, or downloads at both the team and individual levels. Always be prepared for inspections, as our compliance score highlights the engagement levels of each site or study team member with relevant study information. This proactive approach directs you to areas of lower compliance within your study, fostering ongoing improvements in risk management practices. In just a few hours, we can set up a myClin channel for you to explore myClin with your team, making the process exceptionally straightforward. Experience the ease and efficiency that myClin brings to your study management today.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

No details available.

Integrations

No details available.

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial Yes 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support No 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person Yes 

Vendor Details

Company Name

ClinChoice

Country

United States

Website

clinchoice.com/solutions/regulatory-affairs/regulatory-information-management/

Vendor Details

Company Name

myClin

Founded

2008

Country

United States

Website

myclin.com

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance Yes 
Document Management Yes 
Electronic Data Capture No 
Enrollment Management No 
HIPAA Compliant No 
Monitoring No 
Patient Database No 
Recruiting Management No 
Scheduling No 
Study Planning Yes 

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