Clinical Product Return, Reconciliation & Destruction
Assuring Accountability and Compliance
If you are like the hundreds of other innovators we have served, your focus is likely (and understandably) centered on getting your clinical trial underway. However, unexpected study closeout costs are probable if you do not plan for investigational product return, reconciliation, and destruction early in your protocol development process.
Our GMP-compliant procedures and processes ensure compliance, safety, efficiency, and cost-effectiveness.
Comprehensive Clinical Product Return, Reconciliation & Destruction Capabilities
- Certified drug product return, reconciliation and destruction for sites worldwide
- Kit-level and unit-level drug accountability services
- Services can include updating the returned drug status in the Interactive Response Technology (IRT)
- Returns for redistribution to clinical sites
- Schedules I through V controlled drug substance capabilities
- Final manifests and certificates of destruction
Clinical Product Return, Reconciliation & Destruction Solutions
Our highly experienced experts will work with you to design protocol-specific drug product return, reconciliation, and destruction services that assure the utmost accountability for your clinical trial.
Regulatory compliance and cost management are always at the forefront of our pharmaceutical reverse logistics program designs while considering the often unique needs of global sites.
- Turnkey investigational drug product return, destruction, and reconciliation capabilities
- Protocol-specific programs
- Regulatory compliance at the forefront of program designs
- Schedules I through V controlled drug substance capabilities
28
Years Supporting Clinical Programs
200+
Active Programs
2
GMP Facilities
6
Continents with Active Programs
Advantages of Our Clinical Product Return, Reconciliation & Destruction Programs
We offer decades of experience, expertise, flexibility, and adaptability to meet our clients’ clinical product return and destruction needs.
Program Flexibility
We are here to support you if you need help with some or all of your clinical product return program.
Adaptability
Despite the best planning, your clinical product returns program might need to adapt to the unexpected. Our team helps you evolve as required.
Decades of Expertise
Over 27 years, we have worked with hundreds of clients on thousands of programs. This experience gives us the expertise to help your programs run smoothly and efficiently.
Quality & Compliance
Quality and regulatory compliance are always at the forefront, and we are happy to consult with you on these issues and ensure program execution with compliance at the forefront.
Specialized Capabilities & Global Service
Our team is skilled at managing controlled substances, temperature-controlled drugs, complicated reconciliation programs, or handling product returns from global trial sites.
Do You Want to Begin Discussing Your Drug Product Return, Reconciliation & Destruction Strategy?
By planning your reverse logistics program now, avoid unexpected costs when your study ends.