PHARMATIPS

1.0    Objective To describe the procedure to be followed in HPLC analysis and documentation and to insure that good laboratory practice...

Wet granulation forms by binding the powder together with an adhesive, instead of by compaction, bridges are developed between the particl...

Ø   Excipients are those substances which are added to the formulation other than pharmacological active drug Ø   Excipients have slig...

1. Types of process validation Depending on when it is performed in relation to production, validation can be prospective, concurrent...

1.        OOS (out of specification) is the comparison of one result versus a predetermined specification criterion while OOT (Out of ...

1.       Introduction: The validation of the cleaning procedures is establishing documented evidence that the procedure is effective...

INTRODUCTION: Drugs are recognized as ‘essential commodity’ Should always be available to the general public at a reasonable price In...