ICE Global Attorneys Accelerate Your
Clinical Study Start-up & Negotiations
ICE Global is uniquely prepared with a team of attorneys and globally skilled professionals who have vast experience with clinical trials. Our attorneys average 10+ years of experience in the industry, each. We understand the process, from negotiating fair market value, to global contract templates for over 60 countries, and everything in between.
Clinical Trial-Related Agreements
Legally Trained and Clinically Experienced. We offer development, study logistics support, global negotiation, and other contract-related matters, including, but not limited to:
- Advisory Board Agreements
- Amendments
- Ancillary Agreements
- Clinical Trial Agreements
- Commercial Agreements
- Data Processing Agreements
- Informed Consent Forms
- Master Clinical Trial Agreements
- Licensing Agreements
- Material Transfer Agreements
- Non-Disclosure Agreements
- Vendor Agreements
We Are Uniquely Positioned With A Sole Focus on Understanding, Preparing For, and Surmounting Global Challenges to the Execution of Clinical Trial Agreements.
- Ready for worldwide legal and regulatory processes and requirements
- Template development by region, country, and site
- Constant monitoring for legal and regulatory changes
Skilled Budget Negotiators
ICE Global Uses Data Intelligently To Assess FMV For Your Organization’s Research Contract.
We leverage site-specific negotiation experience with an industry leading tool to forecast acceptable budget terms and reduce cycle times. By starting the process with a Fair Market Value (FMV) budget, we make the negotiation cycle more efficient.
We Ensure Your Organization’s Budgets Are Fair and Defensible.
- Site and investigator budget development
- Prepared with planned fallback negotiation parameters
Site Payments
- Utilization of ClinRun, a purpose-built platform for site payments
- Tracking and management of payments from portfolio to site level
- Robust modeling and forecasting capabilities
Consulting and Staffing Solutions
Consulting services related to strategies and efficiencies in the site contracting process in different countries and/or regions in order to avoid or minimize delays, manage expectations, navigate through communications between parties with different cultural backgrounds and languages, avoid predictable pitfalls, and reduce costs, including:
- Overall management of the contracting process, including budgets
- Efficient communications with all parties involved, considering different languages and cultures
- Efficient communications among internal and external study teams
- Management of vendors involved during the start-up stage
Coaching For Success
The ICE Global Team has an average of 10+ years of experience in global site contracts for clinical research. Partnering with our team will help minimize your organization’s burden by tailoring strategies that work for you and are specific to your studies.
We’ll Get Your Team Up To Speed; We Comprehensively Understand How These Projects Function.
- Clinical teams
- Project management
Broad Legal Assistance
The attorneys at ICE Global are well versed in a wide range of legal areas. By establishing strategic frameworks with your legal and contract teams, we will minimize their volume of work so they can confidently turn their attention to other areas or critical aspects of your clinical trials.
Tell Us About Your Project Or Study
ICE Global Attorneys Accelerate Your
Clinical Study Start-up & Negotiations
ICE Global is uniquely prepared with a team of attorneys and globally skilled professionals who have vast experience with clinical trials. Our attorneys average 10+ years of experience in the industry, each. We understand the process, from negotiating fair market value, to global contract templates for over 60 countries, and everything in between.
Clinical Trial-Related Agreements
Legally Trained and Clinically Experienced. We offer development, study logistics support, global negotiation, and other contract-related matters, including, but not limited to:
- Clinical Trial Agreements
- Master Clinical Trial Agreements
- Data Processing Agreements
- Material Transfer Agreements
- Advisory Board Agreements
- Ancillary Agreements
- Non-Disclosure Agreements
- Client Agreements
- Vendor Agreements
- Amendments
Skilled Budget Negotiators
ICE Global Uses Data Intelligently To Assess FMV For Your Organization’s Research Contract.
We leverage site-specific negotiation experience with an industry leading tool to forecast acceptable budget terms and reduce cycle times. By starting the process with a Fair Market Value (FMV) budget, we reduce the negotiation cycle by up to 30%.
We Ensure Your Organization’s Budgets Are Fair and Defensible.
- Site and investigator budget development
- Prepared with planned fallback negotiation parameters
Internationally Equipped
We Are Uniquely Positioned With A Sole Focus on Understanding, Preparing For, and Surmounting Global Challenges to the Execution of Clinical Trial Agreements.
- Ready for worldwide legal and regulatory processes and requirements
- Template development by region, country, and site
- Constant monitoring for legal and regulatory changes
Coaching For Success
The ICE Global Team includes an average of 10+ years of research, contract and negotiating experience. Let us reduce your organization’s burden by teaching the process and strategies that work.
We’ll Get Your Team Up To Speed; We Comprehensively Understand How These Projects Function.
- Clinical teams
- Project management
Broad Legal Assistance
The attorneys at ICE Global are well versed in a wide range of legal areas. We will take on work in order to reduce your internal team’s burden so they can safely turn their attention to other critical areas of the trial.