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

For a drug product containing more than one drug substance, the information requested for part “S” should be provided in its entirety for each drug substance

 

Separate DMF/CEP/Part II S must be provided for each API for:

i. Finished product contains more than one API

ii. API from different manufacturing site

iii. API from different synthesis route

 

References:

Appendix 6 : Guideline On Regulatory Control Of Active Pharmaceutical Ingredients (APIs)

S(i) : Certificate of Suitability (CEP)
  • CEP Number
  • CEP Issue Date
  • CEP Expiry Date
  • CEP Certificate

References:

Appendix 6 : Guideline On Regulatory Control Of Active Pharmaceutical Ingredients (APIs)

S(ii) : Written Statement
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 2.1.2 : Synthesis Route
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 7.1 : Re-test Period Months
S 7.2 : Shelf Life Months
S 7.3 : Stability Data Attachment
S 7.4 : Storage Condition
S 8 : Drug Master File (DMF)
S 8.1 : Letter of Access

 

National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400

 

 

DISCLAIMER

The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

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  • Last Modified: Friday 13 December 2024, 16:27:32.

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