- Compile dossiers (CTD) for CIS, Middle EAst, Latin America, Europe, USA, South East Asia etc
- Complete support for preparation of necessary documents and registration of products with FDA and answering post submission queries.
- Expert reports, summary and overviews as per EU requirements
- Design, arrangements and monitoring of BA/BE studies, toxicological studies ets. Readily available BE studies see here
- Responses to deficiency letters
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Pharmaceuticals: Ready-to-market formulations |
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Through its extensive network, CAREABILIS LLC assists its customers in finding adequate resources by keeping the costs low to further increase the margins. The capability of CAREABILIS LLC to provide you with these prime cGMP and ISO certified manufacturing locations is derived from an acquired, long term local knowledge and expertise built since the start of the second millennium.
The portfolio offers a choice of FINISHED DOSAGE FORMS (tablets, capsules, slow release formulations, injectables, liquids, syrups, ointments and creams) including registration files.
Our catalogue includes more than 1000 references and is available for Pharma customers on CD-ROM or online.
CAREABILIS LLC offers finished formulations including registration dossiers to its pharmaceutical clients in addition to a large number of available ready-to-market formulations we can further :