The inspector is in the lobby.
Are you ready?
Did the PI get the SUSAR?
How do you know?
The CRA was on site last week.
Where's the trip report?
The site submitted their package last month.
Why isn't it in the TMF? 

The Leading Clinical Oversight Platform

Today, 73% of clinical trial professionals* state evidence of Oversight as the most common gap in study Compliance.

myClin solves this challenge by serving as a central hub for all study documentation making Oversight part of your day-to-day activities, while keeping your study inspection ready at all times.

The myClin Compliance Score measures your study teams’ activity to track and unveil blind spots for future improved compliance.

*Source: myClin 2020 Survey.

“In a typical study you have thousands of people working on the protocol, how do you ensure that they all understand the nuances and details?"

John Silowsky, Clinical Trial Lead

Review your study compliance in five minutes and get detailed recommendations.

START NOW
The inspector is in the lobby.
Are you ready?
The CRA was on site last week.
Where's the trip report?
Did the PI get the SUSAR?
How do you know?
The site submitted their package last month.
Why isn't it in the TMF? 

The Leading Clinical Oversight Platform

Today, 73% of clinical trial professionals* state evidence of Oversight as the most common gap in study Compliance.

myClin solves this challenge by serving as a central hub for all study documentation making Oversight part of your day-to-day activities, while keeping your study inspection ready at all times.

The myClin Compliance Score measures your study teams’ activity to track and unveil blind spots for future improved compliance.

*Source: myClin 2020 Survey.

Review your study compliance in five minutes and get detailed recommendations.

Review your study compliance in five minutes and get detailed recommendations.

“In a typical study you have thousands of people working on the protocol, how do you ensure that they all understand the nuances and details?"

John Silowsky, Clinical Trial Lead

The inspector is in the lobby.
Are you ready?
Did the PI get the SUSAR?
How do you know?
The CRA was on site last week.
Where's the trip report?
The site submitted their package last month.
Why isn't it in the TMF? 

Trusted by Pioneers and Leaders Alike.

“myClin has developed a cloud-based tool to simplify communication and task management between trial sponsor, lead investigator, site manager and service providers in between.”

MedCity News

"myClin makes it simple to centralize and disseminate essential information across our clinical study team."

Vice President, Clinical Operations
Trevena

10,700

USERS

110

STUDIES

38

COUNTRIES

Stay on Top of Clinical Oversight.

Inspection Perspective:
Tales From a Recent FDA Inspection

The expectations of regulatory inspectors are rising over time - requirements are getting tighter and sponsors are expected to make better use of their systems and data. Our speaker has very relevant experience from hosting an FDA inspection (2019) where this reality was clearly illustrated.

Site Perspective:
What sites really think of your study processes

Learn how to include local site reality in how you design your study. In this session you will get the chance to hear from experienced site coordinators about what sites really think of your study processes. This will include how to keep you study moving during the COVID-19 pandemic.

ClinOps Perspective:
So, Oversight When You Can't Visit Sites, Eh?

So, Clinical Operations when you can't actually visit your sites! As if running international GCP trials wasn't complex enough suddenly we can't visit sites like we are used to.

Study Operations – How myClin Streamlines Study Execution

Read this paper from our Use Case Series to understand how myClin can not only streamline the communication with clinical sites, but also dramatically increase engagement and compliance.

Build A Key Opinion Leader (KOL) Community On myClin

myClin, the leading Clinical Trial Knowledge Platform, allows for sponsors to connect more closely with investigators and other investigative site staff in a collaborative, secure, and efficient manner.

Streamline and Accelerate Protocol Development

As a single and secure collaboration channel, the myClin platform can streamline and accelerate protocol development while keeping all parties in sync. On myClin, reviews occur in parallel with everybody seeing contributions from other team members.

Modern and Real-World Study Oversight with myClin

This paper provides a modern definition of oversight and what it involves, and illustrates how the myClin platform builds a strong oversight directly within your study team communication and collaboration channels.

Clinical Trial Knowledge Platform - The Road To Compliance

Regulatory scrutiny in clinical research has intensified in recent years, and there are no signs that the intensity of the regulatory environment is abating.

A Theory on Site Engagement

IT startup helps clinical trial ecosystem communicate

myClin offers virtual communities for sponsors, CROs, sites to stay connected during trials

Streamlined Operational Approaches and Use of e‑Technologies in Clinical Trials: Beat Acute Myeloid Leukemia Master Trial

Inspection Perspective:
Tales From a Recent FDA Inspection

The expectations of regulatory inspectors are rising over time - requirements are getting tighter and sponsors are expected to make better use of their systems and data. Our speaker has very relevant experience from hosting an FDA inspection (2019) where this reality was clearly illustrated.

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Review your study compliance in five minutes and get detailed recommendations.