Cadila Pharma

· To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline.
· To ensure Renewal of registered product prior to validity expiration of Africa countries (Region I).
· To Review Registration and Re-registration dossiers before submission in all Africa countries (Region I)
· To maintain country-wise registered product status for all Africa countries (Region I)
· To co-ordinate with other departments R&D, QA and QC for ensuring the filings & query responses.
· To provide technical support to team for preparation of Registration/Re-registration dossiers and query responses.
· To prepare documents for variation filings as and when required for all Africa countries (Region I)
· To update registration information in SAP & Cadinet for Africa countries (Region I)
· To clear issues of commercial Order related to regulatory department for Africa countries (Region I)
· To review the tender requirements and extend necessary support by providing the required documents and samples.
· To co-ordinate with International country managers for smooth scheduling the registration activity.

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