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Our range of expertise covers:
- The preparation, submission and tracking of complete product registration
dossiers for approval under Directive 91/414/EEC and member states;
- A wealth of experience in preparing IUCLID notifications and dossiers
as required by Directive 98/8/EC;
- The preparation and submission of product registration dossiers for approval under Directive 98/8/EC. Click here for details.
- Advising clients on the impact of REACH plus the preparation of registration dossiers and Chemical Safety Reports. Click here for details.
- The co-ordination of task force programmes. This includes assisting
in the preparation of dossiers, discussions with government officials,
working alongside other notifiers and negotiating with companies
who are members of a task force;
- Due diligence registration audits prior to company purchase;
- Advising clients of policy developments on issues such as data
protection, water pollution, uniform principles, parallel importation,
the classification of active substances and approvals of genetically
modified organisms;
- Analysing the effects of emerging policies on existing product
ranges whilst giving guidance on the implementation of strategies
designed to mitigate unfavourable effects;
- Internal capabilities for preparing all dossiers in Computer Aided
Dossier and Supply (CADDY) format;
- And by linking with the BioChemAlliance
this range of services can be provided on a global scale.
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