Marken API Services
Marken’s network fulfills the global movement of API from the point of manufacturing to CMOs and primary packagers. Marken optimizes API logistics around the globe with continuous temperature monitoring, documented transit custody and a worldwide network of offices, providing end-to-end quality-assured supply chain services.With Marken’s experience and expertise they excel in assisting companies to achieve the most expeditiou…
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Marken’s network fulfills the global movement of API from the point of manufacturing to CMOs and primary packagers.
Marken optimizes API logistics around the globe with continuous temperature monitoring, documented transit custody and a worldwide network of offices, providing end-to-end quality-assured supply chain services.
With Marken’s experience and expertise they excel in assisting companies to achieve the most expeditious movement of API’s across country borders. By working closely with customs officials, licensed customs brokers, and using their knowledge of import and trade compliance regulations, Marken is able to provide their customers with all of the details necessary to achieve the lowest possible duty and avoid delays each time a product is being shipped.
Logistics capabilities offered for all ranges of temperature control include:
- Complete real-time reporting of the status of shipments
- Manufacturing supply chain expertise
- Customs preclearance
- Packaging, documentation and declarations consulting
- Regulatory and import/export license assistance and advice
- Insurance coverage
Securing Provision K Status for a Client’s API Helps to Expedite Shipping and Reduce US Importation Costs
This case study presents an example of how Marken — a global life sciences supply chain solutions company — helped a client avoid inappropriate duty charges and expedite importation of its API into the US.
A Model for Pharmaceutical Supply Chain Quality Agreements
Regulatory agencies around the globe have defined A Quality Agreement (QA) as a written document outlining the roles and responsibilities for the owner of the drug and the Contract Manufacturing Organization (CMO) in terms of basic cGMP regulations. This white paper presents a model for pharmaceutical supply chain Quality Agreements and discusses their importance.
