Who should attend?

This intensive course is intended for those new to the topics of product development 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:
• Research& Development
• Production
• Quality Assurance and Control

Course topics:

• Product Development
• Solid Dosage forms
• Sterile Dosage forms

Learning objectives:

Upon completion of this course, you will be able to:

• Determine the regulatory issues to be considered for process development of dosage forms such as tablets, capsules, and parenteral products, scale-up of the process to manufacturing scale and transfer of technology from R&D to production.

• Assess the associated regulatory issues, equipment selection, cost considerations, and critical need for coordination between R&D, Process Development, Production and Quality Assurance groups in the successful process development of drug dosage forms.

• Define the product development process and the many technologies which must operate together to obtain a successful product

• Explain the basic design of solid, and parenteral products

• Gain insight into product performance as a function of product composition

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