Regulatory Affairs Intern (london) - Only for 6 Months
-
Preparation, compilation & submission of Dossiers in CTD, ACTD as
well as country specific format For African, Southeast Asian, and Latin
America countries like. Kenya, Nigeria, Ghana, Philippines, Myanmar,
Vietnam, Sri Lanka, Cambodia, Guyana, Guatemala, EL Salvador, Tanzania,
Syria, Yemen etc.
- Responding to technical queries related to product registration.
- Evaluation and preparation of post approval supplements to manage the regulatory product as applicable.
- Coordinate and consult with other department for accurate and timely assembly of regulatory document for submissions.
- Knowledge of New Product Development.
- Reviewing technical documents and checking of Artworks as per the countries guidelines.
- Co-ordination with International Customers
- Technical data support to dossier preparation for UK.
- Replying to product based queries on the basis of clinical studies asked by medical fraternity.
- Keeping up-to-date with changes in regulatory legislation and guidelines
- APPLY ONLINE
No comments:
Post a Comment