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QuickUpload1085 20170607133209.jpg
Type Private
Industry Medical Devices
Founded 1999
Headquarters Pennsylvania, USA
Number of employees 51-200 employees

About Us

Clinlogix is a global, full service, Clinical Research Service & Consulting Organization. Providing expert outsourcing services to the Medical Device, BioPharmaceutical and Diagnostic Industry. Offering Best-in-Class, performance based, metric-driven, essential services such as Project Management, Monitoring, Data Management, Safety, Biostatistics, Investigator Site ID, Development & Management, Vendor Management, Contract & Investigator payment management. Clinlogix delivers to client highly experienced Teams of Professionals that are therapeutically aligned,. Services are made available "Just in Time" to clients via a flexible, scalable global platform to fit each client’s unique project needs. Clinlogix optimizes eClinical tools to efficiently and effectively manage, monitor and deliver these services. Offices in USA, Germany, Colombia, UK. [1]

Who is Clinlogix?

Our goal is to facilitate an Innovation Pathway for the Life Sciences. Our expertise is in shepherding our client’s investigative products from the bench to the bedside/concept to cure. Working together with inventors, investors and regulatory agencies early and often to oversee and execute each project. The key to success is pairing them with strong scientific and regulatory leadership with the ability to execute on the strategy.

The goal of Clinlogix is to define, refine, support and execute on this pathway from – First in Human through Commercialization. Our vetted global network, Scientific Advisors/Key Opinion Leaders, and our direct access to Centers of Excellence, support this initiative.

Since 1998 Clinlogix has been providing clients with a sense of urgency – high-quality, client specific clinical development support services to the BioPharmaceutical, Medical Device and Diagnostic Industry worldwide.

How We Work with Clients

Clinlogix prides itself on its Client-Focused Philosophy and our commitment to quality throughout the clinical development process. Our team structure is designed to provide direct communication and accountability between team members and our clients. We ensure that the entire process is open and transparent for all stakeholders – our clients, our investigators, the investigative sites, and our study participants. Our teams are designed to facilitate the sharing of responsibility and ownership on every project, empowering everyone to constantly identify, assess, and manage risk.

We also pride ourselves on being a fully integrated partner with every client we serve, working as a virtual extension of their in-house team. Our hands-on approach facilitates communication and decision-making for effective execution of a clinical development program. Additionally, we employ a novel web-based Virtual Integration Partner™ platform, which lets us seamlessly assemble the people, processes, and technologies necessary to achieve the study’s goals.

Services Offered

  • Trial Management Services

-Project Management

-Clinical Monitoring

-Data Management


-Safety Management


  • Other Services

-Medical Writing

-Grant Management


-Project Rescue

-Quality & Compliance

-Training [2]

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