Headquartered in Paris, with offices in the US and UK, Ennov provides the most original, comprehensive, and cost-effective suite of software solutions for the life sciences industry. From leading pharmaceutical companies to emerging biotechnology companies, we proudly serve over 150 companies and 150,000 users around the world. For more than 20 years, we have been developing innovative, powerful and easy-to-use software for regulated content, data and process management. Our solutions are designed and built to support the entire Life Sciences R&D continuum including Clinical, Regulatory, Quality, Pharmacovigilance and Commercial.
IQVIA Clinical Content Management solutions help improve workflow efficiency, promote collaboration, and help you meet compliance requirements, from planning to archive.
The IQVIA eTMF delivers advanced and sophisticated features and functionality to keep your studies on track and compliant. Countless automated features reduce manual efforts, minimize the need for user input, increase efficiency and reduce risk.
Just in Time GCP supports small and mid-size pharma companies and CROs in managing their Trial Master Files. Whether you are anticipating a regulatory inspection, need resourcing for routine quality oversight of your TMFs or are planning the implementation of a TMF system, Just in Time GCP can support you. We have extensive industry experience in clinical operations and truly understand the complexities of trial management and drug development. We partner with your organization in ensuring that your TMFs are inspection-ready. We take the stress out of TMF management.
Medidata, a Dassault Systèmes company, helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users access the world's most-used platform for clinical development, commercial, and real-world data. Discover more at www.medidata.com, The Operating System for Life SciencesTM.
Phlexglobal are the Trial Master File (TMF) experts, and pioneers in the provision of innovative, flexible and technology-enabled TMF solutions and services.
A specialist provider of electronic Trial Master File (eTMF) solutions and other support services to the global clinical research market, we offer a unique combination of technology, quality and services that deliver a range of flexible, targeted solutions to the life science industry.
TransPerfect provides a collaborative web-based platform for study start-up and eTMF that enables sponsors, CROs, IRBs, central laboratories and other vendors to maintain and update clinical trial documentation in a secure online environment. TransPerfect's Life Sciences division is dedicated to working with clients on a global, collaborative level, supporting a wide range of requirements including product licensing and alliance management, endpoint adjudication, eTMF review/reconciliation, and pharmacovigilance.