Overview
In the notes of Pharmaceutical Product Development, I have given two types of notes, namely Handwritten notes, and Standard notes.
Pharmaceutical Product Development is a Project Work subject in the 8th semester of the B Pharm course, and per the PCI 8th semester syllabus, there is a total of 5 units in this subject.
Download Pharmaceutical Product Development all Units Notes PDFs FREE
Click on the following download buttons below the names of the units to download Pharmaceutical Product Development Both Handwritten and Standard Notes.
In the Pharmaceutical Product Development Notes Pdfs, the following chapters are explained in detail.
UNIT-1
Introduction to pharmaceutical product development, objectives, regulations related to
pre-formulation, formulation development, stability assessment, manufacturing and
quality control testing of different types of dosage forms.
UNIT-2
An advanced study of Pharmaceutical Excipients in pharmaceutical product development
with a special reference to the following categories
I. Solvents and solubilizers
ii. Cyclodextrins and their applications
iii. non-ionic surfactants and their applications
iv. Polyethylene glycols and sorbitol
v. Suspending and emulsifying agents
vi. Semi solid excipients
UNIT-3
An advanced study of Pharmaceutical Excipients in pharmaceutical product development
with a special reference to the following categories
i. Tablet and capsule excipients
ii. Directly compressible vehicles
iii. Coat materials
iv. Excipients in parenteral and aerosols products
v. Excipients for formulation of NDDS
Selection and application of excipients in pharmaceutical formulations with specific
industrial applications
UNIT-4
Optimization techniques in pharmaceutical product development. A study of various
optimization techniques for pharmaceutical product development with specific
examples. Optimization by factorial designs and their applications. A study of QbD and its
application in pharmaceutical product development.
UNIT-5
Selection and quality control testing of packaging materials for pharmaceutical product
development- regulatory considerations.