The
Registration Services
Department
plays a vital role throughout the entire notification process,
from the initiation of a project (determining the data requirements
and ensuring that the correct testing is undertaken) to
preparation of the final dossier, and through to submission
to, and acceptance by, the regulatory authority.
A complete
range of work is undertaken, including:
- Advice on regulatory requirements
- Checking appropriate Chemical Inventories
- Development of notification strategy and testing programme
- Literature searches and review of any existing test data
to ensure adequate compliance
- Consultation with regulatory authorities on the testing
programme
- Preparation of the notification dossier
- Post-notification liaison with Competent Authorities
With over 1500 regulatory projects
successfully completed in the last 12 years, SafePharm has
experience in notification under the current chemical regulation
schemes world-wide.
Our Registration Department has
prepared a number of information sheets which summarize the
main elements of all of the major chemical regulatory schemes
world-wide.
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If you would like to download a copy of
any of these sheets as PDF then please complete the registration
form.
These information sheets are regularly
up-dated, and of course new sheets are added from time to
time as necessary.
You will need to login (using your email
address) to view our sheets in full, please follow the instructions
and verification of your account will be emailed to you.
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