IATA significantly revised the Dangerous Goods Regulations 54th Edition Packing Instructions PI 965-PI 970. This step-by-step approach will help you comply with the revised regulations.
Transportation of biologicals has become increasingly challenging. Understanding DG classification requirements is critical to ensure you are in compliance with the law.
Properly plan and prepare for the relocation and ensure the task goes according to the plan through by determining the ideal timeframe, creating a plan of action and maintaining security.
The Americas regulatory agencies accredited by the Pan American Health Organization (PAHO) as regional reference authorities met on December 14-15, 2016 in Washington, DC to discuss strengthening the regulatory cooperation across the region.
The Indian government has allowed for easier import and export of various biological samples by removing the mandatory requirement of an export and import license for these samples, announced Mr Anup Wadhawan, Director General of Foreign Trade (DGFT), on August 4, 2016. The new ruling will save CROs, biotech companies and research centers significantly shorter import and export approval times.
Large financial institution needed to move an entire Data Center under a tight deadline and with limited budget.
A large commercial airliner was grounded in a popular Caribbean destination during a busy winter holiday season...
A biopharmaceutical company needed to transport a bulk drug substance of a critical nature and value from China to US maintaining Controlled Temperature conditions....