Parenteral product development and aseptic manufacturing can be intimidating to people new to the topics. The approach to formulation and process development is substantially different than for oral and topical medications. Product development and manufacturing must consider how all of the manufacturing processes align to ensure chemical, physical, and microbiological stability with particular attention to proper aseptic technique.

Who Should Attend

• Manufacturing/Production

• Research and Development R&D

• Quality Assurance QA

Course Topics

• Sterile Facility& Services.    

• Sterile Process& Equipment

• Sterile Products Formulation

• Sterile Products Quality Approach

Number of Sessions :

5 Sessions 

Instructor:

SPEAKER

Dr. Shady Nabil

                 Global Pharmaceutical industries

                   20+ years of Sterile Manufacturing experience. 

SPEAKER

Eman sayed

                         Quality Assurance Manager

                   +20 years experience in the quality assurance field, certified CPGP -ASQ.

SPEAKER

Dr. Akram Bashir

                   Branch Manager of Nawah Scientific and the formulation Lab.

                   15+ years working in pharmaceutical R&D field.