NEX2US Newsletter Issue 11 | May 2025
Industry member
Cell, Tissue and Gene Therapy Products
Chinese Proprietary Medicines
Controlled drugs
Cosmetic products
Health supplements
Medical devices
Psychotropic substances and poisons
Therapeutic Products
Traditional medicines
20 May 2025
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Regulatory Updates and Process Enhancements
Therapeutic Products
New Online Tools Launched: Application Timeline Calculator and Cloud-based Platform for Dossier Submission
Release of SG-HSA Specification Package (v1.0) for eCTD Implementation in Singapore
Pilot Programme Launched to Extend E-labelling to Pharmacy only (P) and General Sale List (GSL) Therapeutic Products (TP)
Update of Guidance on Therapeutic Product Registration
Clarification on Criteria for Expediated Review of Pending MIV Applications
Implemented GMP Requirements for Chemical DS Manufacturers
Medical Devices
Change Management Program (CMP) for Software as Medical Device (SaMD)
Milestone in Patient Safety: Phase 2 of Implementation of Unique Device Identifier (UDI) system in Singapore
Supporting Digital Health Product Innovation
Cell, Tissue and Gene Therapy Products (CTGTP)
"SHARE": One-Stop Digital Portal for CTGTP Dealer’s Notice, Class 1 CTGTP Notification and Class 2 CTGTP Registration
Streamlining Access to CTGTP Information
Clinical Trials and Innovation Office
Formalisation of the Innovation Office
Upcoming Implementation of the Principles and Annex 1 of the revised ICH E6 (R3) Guideline on Good Clinical Practice (GCP)
Therapeutic Products and Cell, Tissue and Gene Therapy Products
Launch of new Risk Management Plan webpage (1 April 2024) – with implementation of new online form for safety notifications and revised interactive Singapore-Specific Annex (SSA)
International Collaboration
Access Consortium
Project Orbis
HSA Signs Memorandum of Understanding with the Ministry of Health, Malaysia
Introduction of Swissmedic as HSA’s reference agency
Regulatory Leverage
News and Engagements
Next Generation Medical Devices (NextGen MD) Initiative Webinar
More than 40 under probe after multi-agency raid in Geylang on illegal and vice activities
Good Submission Practice Workshop
Industry Training Workshop on (i) Product Defect Reporting and Recall Procedures, and (ii) Management of Nitrosamine Impurities in Therapeutic Products
Complementary Health Products Training Workshop
HSA Removes Over 3,000 Online Listings of Illegal Health Products in First Joint Operation with Online Platforms
Engaging clinical trial stakeholders on ICH E6 (R3) Good Clinical Practice (GCP) Guidelines
Click on the link below to download the issue in pdf:
NEX2US Issue 11 [PDF, 1095 KB]
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