Part II, Section S : Active Pharmaceutical Ingredient (API) Information Submission

How to enter Part II S from QUEST

Please click  "Details" button to open Section S for each API.

Screenshot_1_Details

Reference Document for Section S
Section A: Quality Overall Summary
Section B: Table of Contents
Section C: Body of Data
S 1.1 : Nomenclature
S 1.2: Proposed Structure
S 1.3 : General Properties
S 2.1 : API Manufacture(s) Name & Address
S 2.1.1 : Other API Manufacture(s) involved
S 2.2 : Manufacturing Process and Process Control
S 2.2.1 : Manufacturing Process Flowchart
S 2.3 : Control of Materials
S 2.4 : Controls of Critical Steps & Intermediates
S 2.5 : Process Validation and/or Evaluation
S 2.6 : Manufacturing Process Development
S 3.1 : Elucidation of Structure and Other Characterisation
S 3.2 : Impurities
S 4.1 : Specification of Active ingredient
S 4.2 : Analytical Procedure
S 4.3 : Validation of Analytical Procedure
S 4.4 : Batch Analysis
S 4.4.1 : Certificate of Analysis (COA) of API
S 4.5 : Justification of Specification
S 5 : Reference Standards of Materials
S 6 : Container Closure System
S 7 : Stability Data
S 9 : Certificate of Good Manufacturing Practice (GMP) for API Manufacturer
S 10 : Other supporting documents

National Pharmaceutical Regulatory Agency (NPRA)
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  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
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