All Courses

web-seminar

The REACH Safety Data Sheet: An Advanced Training for SDS Authors

The REACH Safety Data Sheet: An Advanced Training for SDS Authors
web-seminar

Understanding the Guidance for Identifying Endocrine Disrupting Chemicals in the Biocides and Crop Protection Area

Understanding the Guidance for Identifying Endocrine Disrupting Chemicals in the Biocides and Crop Protection Area
New!
New!
web-seminar

Understanding and Applying the GHS-/CLP-Criteria for Classification and Labelling

Understanding and Applying the GHS-/CLP-Criteria for Classification and Labelling
web-seminar

The Extended Safety Data Sheet (eSDS) - Basics for Creation of Exposure Scenarios and Communication in the Supply Chain

The Extended Safety Data Sheet (eSDS) - Basics for Creation of Exposure Scenarios and Communication in the Supply Chain
web-seminar

Health and Environmental Hazards - Classification and Labelling of Mixtures according to the CLP Regulation

The web-Seminar takes place on day 1 from 9:30 am until 4 pm and on day 2 from 9:30 am until 12 pm.
web-seminar

Globally Harmonized System (GHS) – Classification Criteria and Implementation in Selected Asian Countries

The web-Seminar will take place on day 1 and day 2 from 9 am - 4:30 pm and on day 3 from 9 am to 12 pm.
The web-Seminar takes place in five training units on three consecutive days including breaks.
web-seminar

Chemical Waste - Classification, Transport and Notification Requirements

The web-Seminar takes place in two training units on two consecutive days including breaks.
web-seminar

Cosmetic products in the EU - What you should know about the Cosmetics Regulation (EC) No 1223/2009 and beyond!

The web-Seminar will take place in two sessions (2 hours per session).
on-site

Basics of Transport Classification with Focus on ADR

Basics of Transport Classification
web-seminar

Gaining Expertise in the Creation of Safety Data Sheets

Gaining Expertise in the Creation of Safety Data Sheets
e-learning

Session 1: Implementation Strategies for IVDR – Timelines and Priorities – Work Packages

This first IVDR e-Learning session is focussed on how to kick-off the implementation planning for the IVDR transition. Based on an exemplary transition plan, priorites as well as work packages...
e-learning

Session 2: When Medical Devices and IVDs meet REACH

This IVDR e-Learning session is focussed on how the REACH regulation on chemicals impacts your IVDs. The session will provide you an idea on how to monitor critical product components and what to do when your IVD contains substances of concern or...
e-learning

Session 3: Classification under IVDR – Challenges and Opportunities

This IVDR e-Learning session is focussed on potential re-classifications of your IVDs and the respective impact on your conformity assessment procedures. Based on practical examples, we walk you through the actions and steps to be taken...
e-learning

Session 4: Roles and Responsibilities of Economic Operators under the IVDR

This e-Learning session is focused on the impact of the IVDR on economic operators such as manufacturers, importers and distributors. It helps you understand how obligations were shifted and provides answers to the most commonly asked questions...
e-learning

Session 5: Performance evaluation and clinical evidence under the IVDR

This e-Learning session is focused on how to analyse data to establish and/or verify of the scientific validity, the analytical performance and the clinical performance of your IVD device in order to prepare...
e-learning

Session 6: Update of the Technical Documentation Under the IVDR

Within this e-Learning you will learn how to efficiently update your Technical Documentation, how to handle the need for adapted and/or new reports and how to incorporate the new requirements into your existing structures.
e-learning

Session 7: Post-market surveillance and vigilance under IVDR

Within this e-Learning you will learn what the new requirements for post-market surveillance (PMS) and vigilance are under the IVDR and what the new requirements on trend reporting and post-market performance follow-up (PMPF) include. In the bonus...
e-learning

Session 8: EUDAMED and UDI under IVDR

Within this e-Learning you will get an overview on the main objectives, the underlying regulations, important stakeholders and the overall structure of EUDAMED (European Database on Medical Devices) and the UDI (Unique Device Identification) system...
e-learning

Session 9: IVDR – Hands-on session with a virtual IVD example from IVDD to IVDR

Within this e-Learning we will take you by the hands to show you based on a virtual example what points need to be considered when starting the IVDR transition adventure – from the initial thoughts up...
web-seminar

Analysis of Ecotoxicological Experiments with R (for R beginners and advanced users)

The web-Seminar will take place from 10:00-15:00 h CET on both days (incl. breaks).
New!
on-site

Authorisation of Biocidal Products in the EU

Biocidal Products & EU
web-seminar

Authorisation of Biocidal Products in the EU and More – Best Practice Steps to Navigate the Biocidal Products Regulation and Get Your Product to the Market

Authorisation of Biocidal Products in the EU and More – Best Practice Steps to Navigate the Biocidal Products Regulation and Get Your Product to the Market
on-site

Basics of Hazardous Substances

Basics Hazardous Substances
New!
web-seminar

Basics of Transport Classification with Focus on ADR

The web-Seminar will take place from 9:00-17:00 h CET, including breaks.
New web-Seminar!
New!
on-site

Design Process versus Design Control "Europe meets USA"

Design Process vs. Design Control "Europe meets USA"
New!
on-site

Dietary Safety & Risk Assessment

Dietary Safety & Risk Assessment
on-site

Ecotoxicological Assessment of Industrial Chemicals

Ecotox Industrial Chemicals
New!
AwSV – the new regulation!
New!
on-site

IUCLID 6 Member Dossier

IUCLID 6 Member Dossier
New Release IUCLID 6.4
New!
New!
New!
New!
on-site

Proper Packaging and Shipping of Dangerous Goods

Shipping of Dangerous Goods
New!
web-seminar

REACH for Downstream Users, Distributors and Importers of Articles

The web-Seminar takes place in two training units on two consecutive days from 9:00 - 14:00 including a lunch break.
New web-Seminar!
on-site

REACh: Reading and Understanding Exposure Scenarios

Exposure Scenarios - Part 1
New!
New!
New!
New!
web-seminar

Transport Classification Advanced - with Focus on ADR, RID, ADN, IMDG and IATA for the International Multimodal Transport of Dangerous Goods

Transport Classification Advanced - with Focus on ADR, RID, ADN, IMDG and IATA for the International Multimodal Transport of Dangerous Goods
New web-Seminar!
New!
New!
New!
e-learning

Session 3: Recordkeeping Requirement Concerning Alleged Adverse Effects under Section 8(c)

Understanding the statutory requirements and record keeping responsibilities under TSCA section 8(c) and establishing an internal 8(c) program is essential for a company’s overall TSCA compliance program.
e-learning

Session 1: Overview of Key Regulatory Requirements for Industrial Chemicals in the U.S.

This session will provide a high-level overview of the Toxic Substances Control Act (TSCA)
e-learning

Session 2: New Chemical Notification Process under TSCA Section 5

Understanding the recent paradigm shift in the US new chemical review framework and the current scientific assessment process will assist companies with proper business planning and helps to ensure chemicals get to market in a timely fashion.
e-learning

Session 4: Reporting Substantial Risks to Health or Environment under Section 8(e)

Manufacturers, importers, processors and distributors of chemical substances in commerce have a reporting obligation under TSCA section 8(c) when new information is obtained that potentially indicates a conclusion of substantial risk to health or the envi
e-learning

Session 5: Export Notification under TSCA Section 12(b)

Exporters of certain industrial chemical substances or mixtures are required to notify the U.S. EPA of export activities and it is important to understand the statutory requirements and the notification process.
e-learning

Session 6: Import Certification under TSCA Section 13

Importers of chemical substances or mixtures into the U.S. must make a certification regarding TSCA compliance before beginning import activities.
e-learning

Session 7: What Type of U.S. New Chemical Submission is Right for You?

The type of new chemical submission and U.S. notification strategy has become increasingly important with the changes to TSCA Section 5 under the Frank R. Lautenberg Chemical Safety for the 21st Century Act.
e-learning

Session 8: Polymers and Polymer Exemptions

Certain types of polymers may qualify for reduced regulatory requirements under the U.S. Toxic Substances Control Act.
e-learning

Session 9: TSCA Information Requirements and the Notification Form

It is not always clear from the new chemical notification forms what type of information is important to provide the U.S. EPA to properly inform the risk assessment and reduce delays.
e-learning

Session 10: Using Predictive Methods to Conduct a Preliminary Hazard, Exposure and Risk Assessment

This session will highlight available freeware tools that can be used to conduct a preliminary risk assessment before submitting new chemical notifications to the U.S. EPA to anticipate potential regulatory concerns and identify critical outcomes.