A compliance audit is a comprehensive review of an organization's adherence to regulatory guidelines. Audit reports evaluate the strength and thoroughness of compliance preparations, security policies, user access controls and risk management procedures over the course of a compliance audit.
A quality management system (QMS) is a collection of business processes focused on consistently meeting customer requirements and enhancing their satisfaction. It is expressed as the organizational goals and aspirations, policies, processes, documented information and resources needed to implement and maintain it.
Scope: The course deals with different basic pharmaceutical formulation aspects.
Objectives: Upon the completion of the course student shall be able to
1. Understand colloids, rheology, micromeritics and drug stability.
2. Know the principles of formulation preparations.
3. Demonstrate the method of preparation and evaluation of dosage forms.
Scope: The course deals with the various physica and physicochemical properties, and principles involved in dosage forms/formulations. Theory and practical components of the subject help the student to get a better insight into various areas of formulation research and development, and stability studies of pharmaceutical dosage forms.
Objectives: Upon the completion of the course student shall be able to
1. Understand various physicochemical properties of drug molecules in the designing the dosage forms.
2. Know the principles of chemical kinetics & to use them for stability testing and determination of expiry date of formulations.
3. Demonstrate use of physicochemical properties in the formulation.
development and evaluation of dosage forms.
