Pharm-D
MSc EU Regulatory Affairs
Executive Regulatory Affairs
Wilshire Laboratories (Pvt.) Ltd.
124 Kotlakhpat Quaid e azam Industrial Area, 54000 Lahore (Pakistan)
▪ Compilation of Dossiers by gathering, evaluating, organizing, managing and collating information in a variety of formats. Specific focus on stability data and validation reports. Worked with Ac td and CTD format according to FDA, ICH and WHO guidelines.
▪ Participation in arranging documents such as COPP, Free Sales, GMP & DML certificates.
▪ Participation in attaining ISO certificates.
▪ Participation in the preparation of WHO inspections.
