Training courses that have been hold by A. Mehdizadeh, PhD, for pharmaceutical industry:
Physical pharmacy
USP for beginner
USP for advanced
HPLC seminar for pharmaceutical chemists
GC seminar for pharmaceutical chemists
Impurities and analytical methods to determine impurities in API and pharmaceutical products
Preparation of marketing authorization dossier according to ICH-CTD format
Tablet and Capsule formulation
Semi solid formulation
Oral Liquid formulation
Advanced GMP for finished products
Advanced GMP for API
GLP principles in pharmaceutical laboratories
Validation Master Plan
Validation of water systems
HVAC validation
Process Validation
Analytical Method Validation
Equipment Qualification
Good storage practices (GSP) and good distribution practices (GDP)
And Following Training Courses
Training Course
GLP
Pharmaceutical Waters
OOS (Out Of Specification)
CTD (Common Technical Document)
USP
USP and QC
Advanced GMP
USP and tablet standards
GMP Self Inspection
Continued (training courses)
GLP & 17025 Requirements
Self-inspection
GMP, API, ICH Q7A
Basic GMP
Cleaning Validation
Basic HVAC
CTD, Module 3
GMP-API
Parenteral GMP
Tablet and Capsule technology
Quality Management in Pharmaceutical
GMP-PIC/S
USP and semi-solids
Sampling procedures
Clean rooms and ISO
Microbiological testing
CTD and module 1
Water purification systems
Validation of water purification
Good Practices for QC Laboratories
Advanced GLP
Stability testing in pharmaceutical products
Good Storage Practices (GSP)
Good Distribution Practices (GDP)
US-GMP
IPQC
Quality Risk Management
Sterile GMP
GLP and Safety
Temperature Mapping in warehousing
Safety in Analytical Lab
Advanced HPLC
Premises in Pharmaceuticals
Courses Training
Pharmaceutical Analysis
Gas Chromatography, GC
Liquid Chromatography, HPLC
Solid Phase Extraction Methods
USP courses
Physical Pharmacy
Micromeritics
Rheology
Pharmaceutical Development
Nano-technology
Pelletization
Tablet Formulation
Semi solid Formulation
Regulatory Affairs
GMP courses
GLP courses
GSP courses
GDP Courses
Validation Master Plan, VMP
Analytical Method Validation
Process Validation
Validation of Water System
Diplomas
Pharm.D. and Ph.D. from Tehran University of Medical Sciences
Personal Information
Place of Birth: Tehran, Iran
Date of Birth: 09/05/60
Nationality: Iranian
Marital Status: Married
Publications
Serial Books, Industrial Pharmacy, First volume: Pre-formulation and Tablet and Capsule Formulation, Industrial Pharmacy, Second volume: Physical Pharmacy: Polymers, Rheology and Interfacial Phenomena, Industrial Pharmacy, Third volume: Good Manufacturing Practices, GMP, for Pharmaceutical Industry, Industrial Pharmacy, Forth volume: Quality Management and GMP for Drug Substances and Products, Stability Studies: Stability Testing of Drug Substances and Products, Quality Assurance Establishment in Pharmaceutical Companies, Documentation in Pharmaceutical Companies, GLP, Good Laboratories Practices, Pharmaceutical Microbiology, Section One, Pharmaceutical Microbiology, Section Two, Tablets and Capsules, Technology and GMP of Manufacturing of Sterile, Aseptic and Hazardous Pharmaceuticals, Cleanrooms standards according to ISO
International articles, full paper, Design and in vitro evaluation of new matrix, drug-in-adhesive and reservoir formulations of fentanyl transdermal patches, Introducing a full validated analytical procedure as an official compendial method for fentanyl transdermal patches, Effects of pressure sensitive adhesives and chemical permeation enhancers on permeability of fentanyl through excised rat skin, Determination of critical manufacturing parameters on drug release of fentanyl reservoir transdermal patches, Effects of different polymers on dissolution of carbamazepin, Preparation and Skin Permeation Study of N, N- Diethyl- meta-Toluamide Semi Solid Formulations, A Rapid, Simple, Liquid Chromatographic-Electrospray Ionization, Ion Trap Mass Spectrometry Method for the Determination of Finasteride in Human Plasma and its Application to Pharmacokinetic Study
Posters and short articles, A Validated and Compendial Method for Determination of Drug Release of Fentanyl Transdermal Patches, Evaluation of rheological behavior of hydroxyethyl cellulose on drug release of fentanyl reservoir patches, Extended Release Charcterizations of Diclofenac Sodium Pellets Using Ethyl Cellulose and Acrylic Resins as Retardant Polymers, Design of Liposomal Gel of Diclofenac Diethylamine, An Investigation into the Effects of Solvents and Surfactants on the Solubility of Acetaminofen
Certification
PhD
Timeline
General manager
Aani Darman Pharmaceutical Co.
01.2016 - 01.2018
Managing Director and Lecturer
Ofogh Pharmed Educational Institute
01.2009 - Current
Technical Manager
Ofogh Pharmed R&D Institute
01.2001 - Current
Technical Consultant and advisor
01.2000 - Current
R&D Manager
Share Daru R&D Institute
01.2000 - Current
Plant manager & QC Manager
Hakim Pharmaceutical Co.
01.2000 - 01.2004
QC Manager
Iran Hormone Pharmaceutical Co.
01.1990 - 01.2000
R&D Manager
Hakim Pharmaceutical Co.
01.1987 - 01.1990
R&D Manager
Sobhan Pharmaceutical Co.
01.1985 - 01.1987
Pharmaceutical Analytical Expert
Food & Drug Quality Control Laboratory of Iran MOH