NPRA Banner

               
Product Search   QUEST3+ System   Enquiries   Sitemap  

Pre-Membership Module

The Pre-Membership module allows unregistered users to access our online forms. This page is intended for users who are not yet full members and need access to pre-membership forms linked to the QUEST3+ system.

The available forms include:

  1. QUEST3+ Full Membership Application Form
  2. QUEST3+ Membership Slip / Status
  3. Market Sampling Form
  4. In-House Application
  5. Health Professional Adverse Drug Reaction (ADR) Form
  6. Consumer Reporting Form for Side Effects to Medicines or Vaccines

To access these forms, you must register as a Pre-Membership user. Registration is free. Please note that this account is separate from, and not related to, the QUEST3+ USB Token account, including the username and password.

Image

Full Membership Application

To conduct transactions for product registration, variation, licensing, renewal and other related transactions, you must register your full membership and purchase your digital certificate in the form of USB token. Once you have obtained and installed your digital certificate, you will be able to conduct your transactions in QUEST 3+.

Membership Slip / Status

You can use this form to check your full membership application status.

Market Sampling

A one-time entry of cosmetic product(s) which have not been notified solely for the purpose of test market or aesthetic studies to ascertain whether the products are well perceived by a potential group of consumers or manufacturers. These products SHALL NOT BE USED FOR COMMERCIAL SALE.

In House Evaluation

In-house evaluation is a process where product samples either from Research and Development (R&D) or production line, are evaluated by the company for the purpose of product selection, in-house sampling or demonstration. These products may also be actual products that are readily available in the country of origin. These products SHALL NOT BE USED FOR COMMERCIAL SALE.

Adverse Drug Reactions (ADRs)

Please report ALL suspected Adverse Drug Reactions (ADRs) (including those for traditional products) and Adverse Events Following Immunisation (AEFIs) to the National Centre for Adverse Drug Reactions Monitoring.

ConSERF Online Form

If you, or someone you care for, experience any side effects to medicines or vaccines, please report to the NPRA by clicking the tab below. Your reports help improve the safe use of medicines in Malaysia.

 

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.

Site Last Modified

  • Last Modified: Thursday 21 November 2024, 14:55:22.

Search

Main Menu English