Webinar : Clinical Supplies Technology and IRT Standardisation Every study is special, but when it comes to building an IRT system do we really need to re-invent the wheel every time we pick up a new study protocol?
Webinar : Vendor/CRO Oversight How effectively are you doing? Vendor/CRO Oversight is sponsor responsibility and accountability. Vendor Oversight is a high level but an intellectual task which needs right plan, approach and good technology support
Webinar : Successful IRT Partnerships Given the specialist nature of IRT systems, it is now almost impossible for mid and small-sized pharma companies.
Webinar : Reduce Build Time of IRT Systems As we move deeper into the 21st century, technologies available to clinical research teams are evolving at an ever-increasing rate. Whilst this evolution allows clinical trials
Webinar : Developing IRT & UAT : Making The Most of Your Vendor Partnerships The partner companies we work with are critical to our success and never more so than when we select and cooperate with an IRT service provider.
Webinar : Best Practices on IRT and Clinical Supplies Management IRT systems are critical to correct randomization and efficient drug supply management but too often they are an afterthought for a team juggling many conflicting priorities.
Webinar : Are you ready for RBM: process and technology wise ? With the FDA and EMA Risk-Based Monitoring (RBM) guidances as well as the upcoming ICH E6 (R2) changes, are you ready for RBM? This webinar will help you assess
Webinar : Risk Management in Clinical After issuance of the guidance document ICH Q9 - Quality Risk Management in 2006, there was an expectation that every discipline within the pharmaceutical industry
Webinar : CRO - Clinical Vendor Oversight Webinar CRO/Vendor oversight should support sponsor regulatory requirements and cost containment. This balance requires a risk-based approach at the system and project level.