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Introducing Marken Monarch

8 June 2023

Today, Marken announced the launch of the Marken Monarch, a product of our dynamic new partnership with SkyCell shipping critical...

Marken Regulatory Update: New U.S. Customs Postal Code Requirement

7 February 2023

Author:  – Reynaldo Roman, Senior Director, Regulatory Compliance As of March 18th, 2023, importers of goods from China to the...

New Import Control System 2 (ICS2) requirements for shipments entering or transiting the European Union

17 January 2023

Updated on 31 January, 2023 Author: Anna Cesar – Manager, Regulatory Compliance EMEA Effective March 1, 2023, Economic Operators will...

Marken Reaches Agreement to Acquire The Medical Courier Business of Cedra Express, Expands Direct Presence in New Zealand

1 August 2022

Marken, a critical part of UPS Healthcare, has reached agreement to purchase the medical courier business of Cedra Express, a...

UK Consultation on Proposals for Legislative Changes for Clinical Trials

12 May 2022

Author: Anna Cesar – Manager, Regulatory Compliance EMEA The United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA) has ran,...

CDC Noninfectious Certification Statement

20 April 2022

Recently the Centers for Disease Control (CDC) reminded the trade community that shipments of noninfectious diagnostic specimens must be accompanied...

FDA Launches New 24/7 Drug Entry Review Pilot

24 March 2022

Author: Anna Cesar – Manager, Regulatory Compliance EMEA From March 13, 2022, through June 13, 2022, the Food and Drug...

Canada New Client Portal

23 July 2021

Author: Anna Cesar | Regulatory Compliance Associate The Canada Border Services Agency (CBSA) is modernizing and streamlining the process of...

UPS Healthcare Partners with THREAD to provide decentralized clinical trials technology.

1 July 2021

New, comprehensive in-home visit solution provides seamless digital experiences for clients and patients for decentralized clinical trials Research Triangle Park,...

The New European Medical Device (MDR) and In-Vitro Regulation (IVDR)

25 May 2021

Author: Anna Cesar | Associate, Regulatory Compliance The transition period for the new European Medical Device (MDR) and In-Vitro Regulation...

India: New Mandatory Pre-Arrival Clearance Procedures

30 March 2021

Author: Reynaldo Roman | Senior Director, Regulatory Compliance India’s Central Board of Indirect Taxes and Customs announces a new rule...

UPS Healthcare Continues Investment in Personalized Medicine

11 February 2021

Expands Global Cell and Gene Services Capacity  Research Triangle Park, NC, February 16, 2021 – UPS Healthcare announced today an...

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Understanding why we must adapt, continuously asking ourselves how we can change what matters is how we keep on delivering it.