Knowledge Center
How can we help you
Latest News
Join IDBS at the Pistoia Alliance conference as Ken Forman explores how organizations can transform a documented CMC ontology into a GxP-qualified operational framework. Learn how linking ontology to experimental data enables structured, submission-ready information, improving data exchange, regulatory compliance, and the efficiency of CMC processes.
Biopharma organizations have invested heavily in managing CMC data, yet many continue to face a less visible challenge: preserving the knowledge behind critical development decisions. As products progress through development and teams evolve, maintaining scientific context can become just as important as maintaining the underlying data.
IDBS i3 2027 brings together life sciences leaders to explore how connected data, AI, and modern informatics are transforming scientific innovation. Join us in Woking for 1.5 days of customer stories, expert insights, interactive sessions, and networking opportunities.
Join us at i3 Japan and be part of the conversation shaping the future of BioPharma in Japan. Hear real-world case studies from IDBS users and gain insights from IDBS experts on our solutions.
Choose the content type
Search Results (725)
In the news
CMC regulatory submissions: Why knowledge continuity matters
Biopharma organizations have invested heavily in managing CMC data, yet many continue to face a less visible challenge: preserving the knowledge behind critical development decisions. As products progress through development and teams evolve, maintaining scientific context can become just as important as maintaining the underlying data.
Read More
Blog
Six reasons to transition from on‑premise to a cloud‑based laboratory data management system
We dig deep into some of the compelling reasons to move from on-premise to a cloud-based laboratory data management system.
Read More
Blog
Why CMC continuity is the missing link between development and manufacturing
Discover why CMC continuity is the missing link between development and manufacturing, and how preserving connected product and process knowledge helps reduce handoff risk, accelerate tech transfer, and strengthen manufacturing readiness.
Read More
Blog
Why the CRO–Sponsor relationship is becoming a strategic advantage in bioanalysis
As bioanalytical studies grow more complex, transparency is emerging as a strategic advantage. Explore how CROs and sponsors working from a single source of truth can accelerate development without compromising quality or compliance.
Read More
Blog
The playbook for growing CDMOs: how scaling contract development & manufacturing companies can win, and keep, sponsor business
A succinct, practical guide for CDMOs that are navigating digital maturity, cost management, and competitive differentiation
Read More
Blog
How connected bioanalytical context management strengthens bioanalytical decision-making
Bioanalytical studies generate more than results. They create a chain of scientific and operational context that must remain connected from study design and method execution through review, reporting and reuse. Explore how bioanalytical context management helps CROs and sponsors improve traceability, accelerate study delivery and build trusted, AI-ready evidence.
Read More
Blog
Why AI-ready bioprocess data starts at the bench
Too much scientific data lives in disconnected systems, free text or spreadsheets. Without capturing structure and context at the bench, it is hard to reuse data for analytics, automation and AI at scale. Discover how to move from fragmented records to reusable scientific insight.
Read More
