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Robotic Arms

Machinery Regulation and NRTL Certification - Requirements in EU and USA

The new EU Machinery Regulation brings changes compared to the requirements of the current Machinery Directive and the obligations of various operators. Even though the Machinery Regulation does not enter into force until January 20, 2027, you should start preparing now! In the training, we review not only the EU requirements, but also the US requirements for the electrical safety of machines. The training is aimed at machine manufacturers, sellers, users and importers, as well as all companies supplying machines to the United States.
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Doctor with an animated heart in his hand

ISO 13485 MDR Internal Auditor

This course is designed to familiarize quality and regulatory professionals, engineers, designers and management with the requirements for internal auditing of ISO 13485 quality systems. The objective of this course is to provide the skills and knowledge required to conduct internal audits as required by ISO 13485 and Medical Device Regulation.
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SGS Oil Gas Chemical Antwerp Belgium

SGS 2024 Annual General Meeting of Shareholders

On March 26, 2024, SGS will hold its Annual General Meeting of shareholders.
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Detox water cocktail

Global Food Safety Conference 2024

Join us for the 2024 GFSI Conference in Singapore and be part of the largest collaborative conversation on food safety advancements.
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Skyline Network Technology Concept

Embedded World 2024

Join SGS at Embedded World in Nuremberg and explore the latest products and solutions in hardware and software design, IoT, security, and applications in the global embedded systems industry.

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Nourishing Cream

in-cosmetics Global

Meet our experts at booth 1S80.
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Variety of Seafood

Seafood Expo Global 2024

Meet our experts at Seafood Expo Global and learn about our range of seafood testing, inspection, certification and technical services.
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SGS Chemical Laboratory Testing Hrth Germany

SGS 2024 Q1 Sales Update

On April 26, 2024, SGS will publish its Q1 sales update.

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Medical Doctor and stethoscope in hand touching icon

MDSAP Requirements

The Medical Device Single Audit Program (MDSAP) is a certification system that enables a medical device manufacturer to meet regulatory requirements through one annual audit. MDSAP countries are Canada, USA, Australia, Japan and Brazil. Of these, Canada requires MDSAP certification for market approval, but MDSAP certification is also useful in the markets of other participating countries. One of the biggest benefits of the program is a significant reduction in the number of regulatory audits of the MDSAP countries.
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Close up of Wheat Grains

GrainCOM24

Connect with our experts at GrainCOM24 in Geneva.
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