Hassan Mostafa, Certified SSBB, CQM/OE, PM, BPMA, LA in ISO Stds., etc And TQMD.
Hassan is TQM Director in Pharmaceutical manufacturing Facility with a> 20 years experiences and proven track of pharmaceutical manufacturing facility, design, leading Quality division, executing and authorizing all Qualification and validation studies in the Pharmaceutical plant within national organization.
Registered professional Trainer for GxP in pharmaceutical manufacturing and medical device regulatory affairs following MHRA, FDA, ICH, TGA, GCC..etc - in MENA region. Co-founder & Technical Director of REYADA PRO, Pharma&Quality Experts SAE, Consultation and turnkey projects for pharmaceutical sector in Egypt, Certified LA for ISO QMS, EMS and OHSAS from IRCA - UK, QIC and Smart Academy - Sweden, Certified Lead Assessor for GMP Food processing, lead assessor for ISO 22000 from QIC - UK, Certified lead auditor for all auditing programs from Qualitas international certification Ltd. UK, Arab Quality Maker "AQM" Quality Expert, professional Trainer and Consultant in Dubai & Sudan.
Accredited Advisor in TQM and ISO standards for training and certification from Smart Business Academy AB. Sweden professional Accreditation Membership, Certified Business Process Modeling and Analysis from HPI - Germany, > 20 years team leadership of cGMP, Solid Knowledge of cGMP regulations and Project leader for upgrading the pharmaceutical plants to attain GMP license and MAH from relevant international authorities, worldwide discipline, such as: EMEA, EMA, PICs, MHRA, FDA, WHO, TGA, ICH, etc.], technical/Quality consultant & professional trainer of GLP, GCP, QA, QS system drug research center for BE/BA.