Know Your Standard Standards under Mandatory Certification Group Wise Classification Ministry/Department Wise Classification
( Sub Sub Group : Hospital Planning )
Total Standards : 19
Revised Standards
New Standards
| S.No | IS Number | IS Title | Amendment | Reaffirmation Year | Document | Action |
|---|---|---|---|---|---|---|
| 1 | IS 10905 : Part 1 : 1984 |
Recommendations for basic requirements of general hospital buildings: Part 1 Administrative and hospital services department buildings | 0 | Download | ||
| 2 | IS 10905 : Part 2 : 1984 |
Recommendations for basic requirements of general hospital buildings: Part 2 medical services department buildings | 0 | Download | ||
| 3 | IS 10905 : Part 3 : 1984 |
Recommendations for basic requirements of general hospital buildings: Part 3 engineering services department buildings | 0 | Download | ||
| 4 | IS/ISO 11979 : Part 1 : 2018/ISO 80369-6:2016 (1 Revision) |
Ophthalmic implants Intraocular lenses Part 1:Vocabulary First Revision | 0 | ---- | Buy | |
| 5 | IS 12377 : 2016 (1 Revision) |
Classification and matrix for various categories of hospitals (First Revision) | 0 | ---- | Download | |
| 6 | IS 12433 : Part 1 : 1988 |
Basic requirements for hospital planning: Part 1 up to 30 bedded hospital | 2 | Download | ||
| 7 | IS 12433 : Part 2 : 2001 |
Basic requirements for hospital planning: Part 2 up to 100 bedded hospital | 0 | Download | ||
| 8 | IS/ISO 15190 : 2003/ISO 15190:2003 |
Medical Laboratories - Requirements for Safety | 0 | ---- | Buy | |
| 9 | IS/ISO 15195 : 2018/ISO 15195:2018 |
Laboratory Medicine - Requirements for the Competence of Calibration Laboratories Using Reference Measurement Procedures | 0 | Jul, 2024 | Buy | |
| 10 | IS/ISO 15198 : 2004/ISO 15198:2004 |
Clinical Laboratory Medicine - In vitro Diagnostic Medical Devices - Validation of User Quality Control Procedures by the Manufacturer | 0 | ---- | Buy | |
| 11 | IS/ISO 15223 : Part 1 : 2016/ISO 15223-1:2016 (2 Revision) |
Medical Devices — Symbols to be Used with Medical Device Labels, Labelling and Information to be Supplied Part 1 General Requirements ( Second Revision ) | 0 | ---- | Buy | |
| 12 | IS/ISO 16142 : Part 2 : 2017/IS/ISO 16142-2: 2017 |
Medical devices - Recognized essential principles of safety and performance of medical devices: Part 2 General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards | 0 | ---- | Buy | |
| 13 | IS/ISO 17511 : 2020/ISO 17511:2020 |
In Vitro Diagnostic Medical Devices - Requirements for Establishing Metrological Traceability of Values Assigned to Calibrators, Trueness Control Materials and Human Samples | 0 | ---- | Buy | |
| 14 | IS 17786 : 2022/ISO 15223-1:2021 |
Medical Textiles Underpad Specification | 0 | ---- | Buy | |
| 15 | IS/ISO 25237 : 2017/ISO 25237:2017 |
Health informatics - Pseudonymization | 0 | ---- | Buy | |
| 16 | IS 3521 : Part 2 : 2021 |
Personal fall arrest systems - Specification : Part 2 lanyards and energy absorbers | 0 | ---- | Buy | |
| 17 | IS/ISO 6016 : 2008/ISO 14937:2009 |
Earth-Moving Machinery — Methods of Measuring the Masses of Whole Machines, their Equipment and Components | 0 | ---- | Buy | |
| 18 | IS/IEC/TR 62366 : Part 2 : 2016/IEC/TR 62366-2:2016 |
Medical devices Part 2 Guidance on the Application of Usability Engineering to Medical Devices | 0 | ---- | Buy | |
| 19 | IS/ISO/TR 80002 : Part 2 : 2017/ISO/TR 80002-2:2017 |
Medical Device Software Part 2 Validation of Software for Medical Device Quality Systems | 0 | ---- | Buy |