Global Regulatory Consultation Services
Global Regulatory Requirements
Navigating US government customs and agencies for shipping drugs, biologics, specimens and APIs is a daunting task, but it is our expertise. We thrive on overcoming regulatory hurdles and challenges before they cause delays or payments.
Regulatory Solutions
- » Correctly Classify your API to Save Time and Money
- » Reduce Customs Headaches and Duties Customs Handling Of Clinical Trials Materials
- » Regulations in Every Region to Expedite Global Shipments
- » Classify API and Pharmaceutical Products to Avoid Overpaying Duties Around the Globe
- » Correct Valuation of API and Drugs for Declaration
Most customs and agency hold-ups can be avoided by careful expert review and planning, including:
- » Identify Risk Windows and Thresholds
- » Specify Best Routes and Timelines
- » Understand Packaging & Handling Requirements
- » Identify Regulatory Implications of Classifications
- » Categorize Import & Export Requirements for Shipping
- » Specify Required Documentation
- » Pre-clearance of Customs
- » Pre-payment of Tariffs and Taxes
When It’s Out of your Hands, It’s in Ours.
To find out more about how Marken’s regulatory expertise can help your clinical trial process, email info@marken.com or fill out our short contact form:
