News & Insights
Delays in Site Start-up = Delays in Study Results
In Part 2 of our study start-up series, ICE Global Consulting’s Head of Site Readiness, Maria P. Ladd, explores how factors across the various study teams can lead to site
Delays in Site Start-up, the Perpetual Cycle
In a multipart series, ICE Global Consulting’s Head of Site Readiness, Maria P. Ladd, explores factors leading to Site Start-up delays. Part 1: Factors for Delays During 18
Announcement: Site Readiness Services Launch
RAPID SITE READINESS Beginning January 2024, ICE Global will offer Site Readiness services with the aim of reducing site start-up times & shedding unnecessary administrative burdens from the Sponsor,
Part 3: Protecting your future Intellectual Property
In part 2 of our series, GDPR Compliance- Improving Your Position, we introduced a growing and ongoing concern arising from transatlantic clinical trial administration and utilization of data under the General Data
Part 2: GDPR Compliance- Improving Your Position
In Part 1 of our series, we surveyed certain challenges in the negotiation of indemnification language in clinical trial agreements. That article, I’m Responsible for What? Indemnification in Clinical Trials,
Part 1: I’m Responsible for What? Indemnification in Clinical Trials
Negotiation of contracts in clinical trials often comes down to a select few commonly contested sections and terms. Behind these negotiations are a range of factors driving decision making including,