How to Access Other in QUEST3+ System ? 

Product Registration >> New Application Form >> Product Validation >> Other Information

• 5.1 Origin
• 5.2 Function 
• 5.3 In the Manufacturing Process
• 5.4 In the Final Product 

• Please select YES if there is any active ingredient, excipient and/or capsule shell derived from human or animal.
• Please specify whether the origin is porcine/ bovine/ ovine or others.
• If OTHERS is selected, please specify the source.

• Please select the manufacturer of the finished product from the database list. If the manufacturer is not listed, please click the ‘Not Listed’ button; upon which, the particulars of the manufacturer should be provided by applicant, along with the manufacturer’s GMP Certificate/ Status
• Please take note that the manufacturer must be listed in the database before applicant may proceed with product registration application. 
• Please ensure the name and address of manufacturer is the same with the GMP certificate attached.

• Please select YES or NO if the manufacturer is contact manufacturer or otherwise.

• An application for a second source may be considered where deemed necessary. 
• Please select YES or NO if the product application is second source or otherwise. 
• If the product is second source, a declaration letter stating that the product is second source, along with justification for second source must be provided. Applicant must also state the first source product by selecting from the database.
• Please refer:  Appendix 8: 8.1.6 SECOND OR THIRD SOURCE

If Yes, please state

a) Manufacturer (repacker) name

b) Manufacturer (repacker) address

c) Certificate of Good Manufacturing Practice (GMP)

d) Packaging Process

Please select YES or NO if the manufacturing of the product involves any repacker or otherwise. If a repacker is involved, please be advised that the repacker must have a valid GMP Certificate to perform such activity.

• Registration of product for export only (FEO) refers to locally manufactured products for exporting purpose only and not marketed locally. This does not apply to imported products meant to be packed/repacked locally and to be re-export.
• Please Refer :
  1. Registration Of Product For Export Only (FEO)
  2. Direktif Kaji Semula Pendaftaran Produk untuk Tujuan Eksport sahaja/ For Export Only (FEO)

• *If Yes, 
• 12.1 Section E Type

• Please select YES or NO, depending whether this is an imported product or otherwise. If imported product, please select Section E Type either Type A (CPP) or Type B (CFS & GMP).

*If Yes, 

• 13.1 State your Premix Form
• 13.2 Manufacturer Name
• 13.3 Manufacturer Address
• 13.4 GMP Certificate
• 13.5 Formulation Process
• 13.6 Manufacturing Process
• 13.7 Specification of Analysis
• 13.8 Certification of Analysis

Please select YES or NO, depending whether this product contains any premix or not. If it does, applicant should state the premix form, manufacturer name and address, and provide its GMP Certificate, Formulation Process, Specification of Analysis and Certificate of Analysis.

Note: Process Validation (Protocol & Report) for API Premix (in Section P3.4)

*If Yes, 

• 14.1 Declaration Letter
• 14.2 Product(s) to be replaced

Please select YES or NO whether this is a replacement product or otherwise. If it is, applicant must attach a declaration letter and state the product(s) to be replaced.

*If Yes, 

• 15.1 Application Letter 
• 15.2 Priority Review Status 
• 15.3 Date of Grant 

Please select YES or NO, depending if the product has priority review or otherwise. If there is priority review granted, applicant should click YES, and provide the Application Letter to NPRA, Approval Letter for Priority Review from NPRA, Priority Review Status and Grant Date. 

Not applicable to biologics. 

Not applicable to biologics. 

*If Yes,

• 18.1 Medical Device
• Please select YES or NO, depending whether this product contain medical device component or not. If YES, applicant should attach the medical device component document.

Please refer :

• Directive No. 4 Year 2017, Ref. (9) dlm.BPFK/PPP/07/25 Jld. 1 : DIREKTIF KUATKUASA PEMAKAIAN GUIDELINE FOR REGISTRATION OF DRUG-MEDICAL DEVICE AND MEDICAL DEVICE-DRUG COMBINATION PRODUCTS
• Guideline For Registration Of Drug-Medical Device and Medical Device-Drug Combination Products