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Han Zuyderwijk

Han Zuyderwijk

Han is the founder and Senior Product Compliance Consultant at Alura Group. He assisted thousands of companies with their product safety and compliance questions.

— 111 posts published
Website
December 2021

France Blocks Wish from Search Engines

November 2021

Amendments Toy Safety Directive

— EU
November 2021

New MDCG guidelines for MDR compliance of older devices and requirements for parallel imports into the EU

— Medical Devices
November 2021

'Philips is liable for health problems' say users of apnea devices.

— Medical Devices
November 2021

Country-Specific Information For EPR Compliance

— ERP
October 2021

Artificial Intelligence, New EU Rules Proposals

— Market Surveillance
October 2021

Amendments To Harmonized Standards Pressure Equipment Directive (PED) 2014/68/EU

— PED
October 2021

Europe: Eight New Substances in the SVHC Candidate List

— ECHA
October 2021

Unfinished Machinery: Who Is Responsible For CE Marking?

— EU
October 2021

UK Postponement Implementation Import Controls on EU Products

— EU
October 2021

Happy World Standards Day!

— IEC
October 2021

What Do You Need To Do To Sell Cosmetic Products In Great Britain

— Cosmetics
September 2021

LEVA-EU Disputes Dutch bill for LEV's

— EMC
September 2021

New EU database gives consumers access to information on hazardous chemicals in products

— ECHA
September 2021

Product Safety & Risk Assessment, a Bayesian Network Approach

— OPSS
September 2021

The effect of transparency, penalty size and business size on safety regulations compliance

— Market Surveillance
September 2021

Smart Products; Consumer Perspective

— OPSS
September 2021

MHRA launches public consultation on future of medical device regulation

— Medical Devices
September 2021

CLP Reform; EU Seeks Input

— EU
September 2021

UKCA mark for medical devices: The practicalities

— UK
September 2021

Decathlon Fined A$1.5m

— Market Surveillance
September 2021

The Future of Quality in Product Safety and Product Compliance

— EU
September 2021

MDR Current Registration Requirements

— EUDAMED
August 2021

UK-Overhaul Privacy Rules

— GDPR
August 2021

‘UK Medical Devices Regulation Needs Reform’

— Medical Devices
August 2021

UKCA Marking Deadline Extended

— UK
August 2021

Permanent AI-Working Group

— Medical Devices
August 2021

Amazon Revises Liability Policy

— Product Liability
August 2021

European Union Harmonized Standards For Medical Devices

— CE marking
August 2021

Digital Therapeutics' Responsible Integration

— Medical Devices