lobna emam mohammed

RA section headFull Time

• Job Details:Preparation of registration files human imported pharmaceuticals products.  submit and follow up the registration files in the ministry of health (C.A.P.A)  Submit and follow up technical files to NODCAR  Prepare the regulatory documents needed to attain the approval of regulatory agencies needed for the registration of pharmaceutical products in addition to acting as the liaison between the company and the regulatory authorities.  Preparing clear arguments, explanations and presentations for regulatory organizations to resolve any issues related to new product licenses, renewals and variations.  Submit and follow up goods analysis at NODCAR until get the approval for release.  Prepare, submit and follow up medical device registration files until get final registration license.  Prepare, submit and follow up files for dietary supplement to NFSA  Performing other duties related to the job as assigned by the direct supervisor  Communicate regulatory information to multiple departments ensure that information is interpreted correctly