Non-Sterile Manufacturing Systems
In-person/ Virtual
WHO SHOULD ATTEND?
THIS INTENSIVE COURSE IS INTENDED FOR THOSE NEW TO THE TOPIC OF TABET& CAPSULE DEVELOPMENT& MANUFACTURING, AND THOSE NEEDING A REFRESHER ON THE TOPICS AS WELL AS THOSE SEEKING CONFIRMATION OF ACCEPTABILITY OF EXISTING PRACTICES.
IT WILL BE OF PARTICULAR VALUE TO THOSE IN:
MANUFACTURING/PRODUCTION
RESEARCH &GMP;DEVELOPMENT
QUALITY ASSURANCE AND CONTROL
COURSE OBJECTIVES
UPON COMPLETION OF THIS COURSE, YOU WILL BE ABLE TO:
LIST THE REGULATORY CHALLENGES THAT MUST BE CONSIDERED AT S.D.F FACILITY.
IDENTIFY THE BASIC CONCEPTS APPLYING TO PROCESSING OF SOLID DOSAGE FORMS DESIGN.
MODIFY AND CONTROL A PROCESS TO PRODUCE PRODUCTS THAT HAVE THE DESIRED PROPERTIE
COURSE TOPICS
INFRASTRUCTURE: A. FACILITIES, UTILITIES &GMP;EQUIPMENT 3. ENVIRONMETAL MONITORING.
NON-STERILE MANUFACTURING SYSTEMS
SOLID PROCESSES & EQUIPMENT
FILLING& PACKAGING
Number of Sessions :
5 Sessions
Instructor:
SPEAKER
Akram Bashir
Branch Manager of Nawah Scientific and the formulation Lab.
15+ years working in pharmaceutical R&D field, working at different pharmaceutical drug manufacturers
SPEAKER
15+ years working in pharmaceutical R&D field, working at different pharmaceutical drug manufacturers
Mohamed Saad Mohamed
Pharma Consultant, VALOR GM
20+ years working in pharmaceutical field, working for different pharmaceutical drug manufacturers, VALOR co- founder
20+ years working in pharmaceutical field, working for different pharmaceutical drug manufacturers, VALOR co- founder