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myLaminin Perspectives
Insights on Research Compliance, Clinical Trials & Data Management


From One Idea to a Connected Research Ecosystem
Five years ago, myLaminin began with a single idea. Today, it has evolved into a connected research ecosystem supporting the complete research lifecycle—from grant submission through publication. Discover how one conversation with a Canadian U15 university transformed our vision, how researchers co-designed our platform, and how myLaminin became a sovereign Research Data Management (RDM) and Clinical Trial Management System (CTMS) built for active science.

Deanne Bassili
Jun 224 min read


CTMS vs EDC vs eTMF Explained: The 3 Clinical Systems Every Research Team Should Understand
Learn the differences between CTMS, EDC, and eTMF and how these essential clinical trial systems work together to improve research operations, data quality, regulatory compliance, and study efficiency. This guide explains the role of each platform, their integration across the clinical trial lifecycle, and how myLaminin's Research Data Management platform combines CTMS capabilities, participant management, eTMF, protocol management, audit trails, and 21 CFR Part 11 compliant

Darina Dragouleva
Jun 163 min read


Managing Protocol Deviations and Amendments in Multi-Site Clinical Trials at Scale
earn how sponsors can manage protocol deviations, amendments, eTMF documentation, and regulatory compliance in multi-site clinical trials under evolving ICH E6(R3) expectations.

myLaminin
May 257 min read


Why Clinical Trial Start-Up Delays Still Happen and How CTMS Technology Is Fixing Them
Clinical trial start-up delays continue to impact site activation, budgets, and timelines due to fragmented workflows across feasibility, contracting, IRB/REB approvals, training, and system readiness. This article explains how CTMS platforms, integrated research systems, and AI-driven automation reduce inefficiencies by centralizing processes, improving visibility, and accelerating trial activation across global clinical research environments.

myLaminin
May 136 min read


ICH E6 (R3) Is Here: What It Actually Means for Clinical Trials and Why It Matters Now
ICH E6 (R3) is reshaping clinical trial compliance across Canada, the U.S., EU, UK, and Australia. The updated Good Clinical Practice (GCP) guideline emphasizes Quality by Design, proactive risk management, audit trail traceability, sponsor oversight, informed consent, data integrity, and inspection readiness. myLaminin helps research teams and sponsors manage multi-site clinical trials with real-time oversight, CTQ monitoring, compliant eConsent, secure audit trails, and val

Deanne Bassili
May 74 min read


Simplifying Research Data Management
myLaminin, the most complete, integrated, and secure Research Data Management (RDM) platform on the market.

Ash Bassili
Mar 11, 20253 min read


6 Impacts of Streamlining the Research Data Collection Process
No matter what field you are working in, good data collection and management isn’t just nice to have, it's essential.

Kian Petroskie
Mar 3, 20254 min read
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