Method development & validation
Development and validation of assay methods for active substances and preservatives, and of related-substance methods, to current pharmacopoeial expectations.
The laboratory that supports our own GMP production also takes outside work. From method development to stability studies, our chemists and chemical engineers run the tests your dossier or your batch release needs.
Development and validation of assay methods for active substances and preservatives, and of related-substance methods, to current pharmacopoeial expectations.
Dissolution method development and validation for oral solid and powder forms.
Long-term and accelerated programmes, with storage conditions and sampling points agreed up front.
Routine physicochemical QC on raw materials, in-process samples and finished product.
Scope, turnaround and pricing are agreed per project. Tell us what you need tested and we will confirm what we can take on.
Our quality-control register covers 162 substances: the active substances and excipients we routinely work with in our own production. If yours appears here, we already know the material.
No substance matches your search. Send it to us anyway and we will tell you whether we can take it on.
This is a list of materials we work with, not a schedule of tests or specifications. Which parameters are measured, to which method and to which limits, is agreed for each request.
Represent Medicavet exclusively in your market with the full export range.
Have our formulations produced under your own brand, from method development to stability.
Storage under GMP conditions with documented control, plus logistics support.
Describe the samples and the tests you need. Our laboratory team will respond with feasibility, turnaround and pricing.
This is an AI assistant, so answers may be imperfect. For specifics we'll connect you with our team.