Expert Technical Support for Seamless Solutions

Reliable technical support for seamless pharamaceutical solutions.

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SARVA PHARMACEUTICALS

TECHNICAL SUPPORT

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DOSSIER COMPILATION AND REGULATORY SUPPORT

Dossier in CTD (modules 1-5 or any requisite module) and eCTD formats for worldwide markets like EU, USA, UK. Dossiers for ASEAN and ROW countries in ACTD as per country specific format, for any dosage form. Dossier reformatting to CTD/eCTD by taking up gap analysis of existing dossiers in line with current requirements. Drug Master file(DMF) for API, Excipients, Packaging Materials.

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TECHNICAL SUPPORT

The impact of industry trends and regulations on the development and manufacture of Healthcare products may cause costly delays in bringing products to market. The need for clear, Up-to-date, Regulatory guidance is more important than ever. We provide a rapid turnaround with complete documentation according to the Guidelines.