Contact Information

Headquarters:
Vänrikinkuja 3 JK 21
FI-02600 Espoo, FINLAND
Tel: +358 (0) 9 412 3055
Fax: +358 (0) 9 412 3049
Email:
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Our Services

At REACHLaw, we work closely with our clients to provide chemical regulatory compliance and product safety solutions to fit each customer and their needs. We help companies to gain market access for their chemical products and we support them with chemical regulations such as: “EU REACH & CLP”, “Turkey KKDIK, SEA & GBF”, “South Korea REACH & GHS”, “Russia REACH" and many more.

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Industry Sectors

Organizations’ needs on chemical regulatory compliance and environmental sustainability vary greatly depending on the company type, industry sector, the size of the organization, the main markets and the organizational capabilities. REACHLaw has developed a set of chemical regulatory compliance solutions to help businesses to navigate the complex regulatory landscape, spearheaded by REACH & GHS.

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The Blog

An online space dedicated to chemical regulatory compliance. The Blog not only offers you updates on what is going on with the different chemical regulations, it is also a meeting point where key stakeholders are sharing their thoughts towards chemical compliance issues and business in a global scale. In The Blog we have guest writers to make sure you get the breadth of topics and services we can offer.

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REACHLaw Webinar

Call to Action for Downstream Users covered by upstream authorisation applications - Webinar

Given that large authorisation dossiers can take close to 2 years to develop, what can you do if your use has been covered by one of these upstream umbrella applications that has only received a 4 years review period from ECHA or the Commission?

Authorisations do not last forever. They are time limited (typically, they get 4, 7 and 12 years of review periods) and are also quite complex, especially the upstream authorisation applications covering hundreds of DUs and complex supply chains like the CTAC and MOCA applications.
20th of September 2018, 2:30PM - 3:25PM

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Latest from the Blog

What to do if you are relying on an upstream Authorisation that only gets a 4 years review period?

Given the experience of some broad upstream applications for Authorisation, like MOCA and the CTAC application covering many hundreds or thousands of downstream users, with complex supply chains and hidden dependencies, what is the next step for companies currently covered by these applications? Initially when the Authorisation process was starting it was envisaged that the process would be similar to...

Registration is done! What's now?

  The REACH & CLP work doesn’t stop with the registration of your substances. On the contrary, a number of on-going registrant activities and ad hoc tasks will need to be carry out for an unlimited time by the registrants to react to relevant changes and keep their dossiers continuously updated due to ECHA’s dossiers compliance checks but also to...

We are exhibiting @ CPhI North America and @ Chemspec India!

Attending CPhl North America or Chemspec India? Come and visit us! We would love to have a chat with you, understand your chemical regulatory compliance needs and provide you with the best possible solution! [caption id="attachment_2141" align="alignleft" width="300"] Chemspec India 2018. Booth C29[/caption] [caption id="attachment_2140" align="alignleft" width="270"] CPhl North America Booth 353[/caption]