|
|
Documentation & Regulations
Why?
No good toxicological or pharmacological evaluation can be achieved without a previous extensive research on the existence and relevance of available bibliographic data.
The regulatory context in which a substance or a product can be marketed can not be ignored either.
We started to proceed in an empirical and aleatory way according to our immediate needs, understanding rapidly that we could not be satisfied with this kind of approach: too many researches, too many databanks, regulatory provisions always on the move, an increasing overlap between legislations from various economic domains. And now the requisite to consider the structure - activity relationships... |
How?
Each of the Evic Members faced this situation; as a consequence the decision was made to centralize this activity in order to keep the Members informed about the evolution of the regulatory provisions in the different countries or at international organizations' level, and to carry out the documentary inquiries they might need. |
|
|
Our Offer
The efficiency of our organization caught our economic partners' attention and brought us to make this service available to them.
Today, we are at your disposal to perform documentary and bibliographic researches on specific subjects, and to make up technical files enabling, according to your needs, the notification / declaration / registration of your substances and products.
Our own structure is reinforced by a network of international partners duly accredited, allowing us to adapt our offer to national specificities.
To get more details about this service of ours, click below... |
|
|
|
