Medical Devices Regulations (MDR)

Nov 19, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Introduction

A complete guide to Brazil Serialization

Nov 8, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Counterfeit

SFDA Dossier requirements

Aug 27, 2021 | Serialization, Pharmaceutical, Regulations, Compliance

What you should know about SFDA classification and Drug registration

Aug 20, 2021 | Serialization, Regulations, Compliance, Aggregation

SFDA is the regulatory body in Saudi Arabia that handles the registrations and approvals for products that are distributed in Saudi Arabia whether they...

Saudi Pharmaceutical Serialization and Aggregation Roadmap for Vision 2030

Jun 4, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Newly Announced Serialization Changes by the Australian Government (TGO 106)

Apr 16, 2021 | Serialization, Pharmaceutical, Regulations, Compliance

Implications of Brexit on the UK Pharmaceutical industry

Apr 2, 2021 | Brexit, Serialization, Pharmaceutical, Regulations, Compliance

The United Kingdom voted to leave the European Union in 2016, but it wasn’t until December 24th 2020 that the details of trade between the two countries...

A Primer on Alert Management Within the EU FMD Regulations

Mar 26, 2021 | Serialization, Pharmaceutical, Regulations, Compliance, Aggregation

Avoiding Mismanagement of Master Data

Feb 19, 2021 | Serialization, Pharmaceutical, Master Data, Compliance, Counterfeit, Blockchain

Securing the Manufacturing and Packaging Supply Chain in a Pandemic

Feb 5, 2021 | Serialization, Pharmaceutical, Compliance, Counterfeit, Covid-19

Since the beginning of the pandemic manufacturers and packaging suppliers have been trying to meet the sudden surge in demands owing to Covid-19. There...