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Registration of generic pharmaceutical specialties
The Regulatory Department has an extensive and consolidated experience in preparation of the registration dossiers and submission to local and EU regulatory authorities, via national or mutual recognition procedures. It has compiled several dossiers with a highly positive approval record even in the most demanding countries.
None of the products will be supplied to countries in which this could be in conflict with the existing patents. However, the final responsibility lies exclusively with the buyer.
© LESVI Laboratorios / Inke. All rights reserved.
© LESVI Laboratorios / Inke. All rights reserved.
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