We strive to provide clinical development and support services with solutions to enhance the performance of their research and development investment. Global transportation, importation and distribution of investigational products, vaccines, clinical trial supplies, as well as related medical equipment are some of the most fragile and time-sensitive commodities. We provide assistance with obtaining Ministry of Health (MoH) permits and import duties.

These valuable products are often the most difficult ones to deal with reliably since near-absolute controlled conditions are required.

Worldwide Biopharma is structured to support the necessary monitoring and strict handling guidelines (with system checks along the way) to offer an unparalleled service. We have a network of GMP compliant facilities and maintain the strictest SOP codes.

First and foremost, Customs is an authority or agency that resides at country level and has the primary responsibility of collection of goods and safeguarding customs obligations/ duties. Shipments will not clear customs unless the paperwork is accurate and complete.

Understanding the world of Customs and its complex language can be a daunting challenge. That’s why Worldwide Biopharma takes over the endless terminology, evolving paperwork and guidelines. This management of customs duties is essential for controlling the flow of goods in and out of a country. Therefore, the customs process begins in the country of origin and ends in the country of destination.

We validate the paperwork and information for each and every shipment in advance, before the cargo leaves our premises at the port of exportation.