Efficiently managing and organizing the vast amount of documentation required for clinical trials is critical for compliance and overall study success. At Lambda Therapeutic Research, we understand this challenge all too well. That’s why we’ve developed an Electronic Trial Master File (eTMF) platform that uses state-of-the-art technology to collect, store, and manage essential documents and data throughout the entire lifecycle of your clinical trial.
Our dedicated eTMF team brings extensive experience, ensuring you have a comprehensive understanding of your study and run it efficiently. Lambda’s eTMF is a robust and feature-packed solution with the ability to compile dossiers according to various global regulatory standards, making the dossier compilation process over 60% faster.
Efficiently managing and organizing the vast amount of documentation required for clinical trials is critical for compliance and overall study success. At Lambda Therapeutic Research, we understand this challenge all too well. That’s why we’ve developed an Electronic Trial Master File (eTMF) platform that uses state-of-the-art technology to collect, store, and manage essential documents and data throughout the entire lifecycle of your clinical trial.
Our dedicated eTMF team brings extensive experience, ensuring you have a comprehensive understanding of your study and run it efficiently. Lambda’s eTMF is a robust and feature-packed solution with the ability to compile dossiers according to various global regulatory standards, making the dossier compilation process over 60% faster.
The Lambda Advantage
Discover the advantages of Lambda's eTMF solution, where technology meets compliance, and efficiency drives success in clinical development.
Stay Compliant and Efficient with Lambda's eTMF:
- Maintains detailed audit trails for transparency.
- Meets rigorous regulatory requirements, audits, and inspections
- Provides centralized management of clinical trial documentation.
- Facilitates seamless exchange of clinical trial materials among stakeholders.
- Streamlines TMF document workflows, quality control checks, and finalizations.
Key Benefits:
- Reduced regulatory risk.
- Flexible rights management.
- User-friendly web-based application.
- Part 11 compliant (21 CFR Part 11 and Annex 11).
- Cost savings from increased filing efficiency and reduced paper.
Why Choose Lambda's eTMF
Expertise
Backed by over two decades of clinical research experience, we have fine-tuned our eTMF solution to cater to the unique needs of the pharmaceutical and biotech industries.
Scalability
Our eTMF system is adaptable to trials of all sizes, ensuring that your document management needs are met, whether it's a Phase I study or a large Phase IV trial.
Support and Training
We provide comprehensive support and training to ensure that your team can leverage the full potential of our eTMF system.
Let's Unveil New Therapies Together
Connect with our experts to leverage our proven track record of clinical research excellence.