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@Shehleeza
Member since August 1, 2014
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Shehleeza

Online Offline
Summary of Product characteristics, Clinical trials, Pharmacovigilance, Analytical reports, CAPA, eCTD, CTD Dossier compilation.
$10 USD/hr
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Portfolio

Recent Reviews

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Experience

Executive Regulatory Affairs

Mar 2015 - Oct 2016 (1 year)

▪ Compilation of Dossiers of Pharmaceutical & Nutraceutical products by gathering, evaluating, organizing, managing and collating information in a variety of formats. Specific focus on stability data and validation reports. Worked with Actd and CTD format according to FDA, ICH and WHO guidelines. ▪ Participation in arranging documents such as COPP, Free Sales, GMP & DML certificates. ▪ Proof reading of Artwork and Labeling.

Education

Pharm-D

2007 - 2012 (5 years)

MSc EU Regulatory Affairs

2016 - 2018 (2 years)

Qualifications

Certificate of Appreciation (2016)

Wilshire Pharmaceutical Laboratories

Co-ordination in acquiring ISO certificate for a Company.

Publications

Sun has no boundary

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