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Foreign pharmaceutical packaging
Foreign pharmaceutical packaging, Total:138 items.
In the international standard classification, Foreign pharmaceutical packaging involves: Pharmaceutics, Aids for disabled or handicapped persons, Packaging and distribution of goods in general, Quality, Services, Aircraft and space vehicles in general, Medical equipment, Fluid storage devices, Burners. Boilers, Domestic safety, Equipment for children, Protection against dangerous goods, HEALTH CARE TECHNOLOGY, Products of non-ferrous metals, Applications of information technology, Freight distribution of goods, Packaging materials and accessories, Laboratory medicine, Products of the chemical industry, Agricultural machines, implements and equipment, Company organization and management.
Association Francaise de Normalisation, Foreign pharmaceutical packaging
- NF H00-016:2010 Packaging - Braille on packaging for medicinal products.
- NF H00-016*NF EN ISO 17351:2014 Packaging - Braille on packaging for medicinal products
- NF H60-251:2015 Packaging - Tamper verification features for medicinal product packaging
- NF H60-251*NF EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging
- FD H00-019*FD CEN/TR 15753:2008 Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people
- NF H00-202:1997 Packaging. Child-resistant packaging. Requirements and testing procedures for non-reclosable packages for non-pharmaceutical products.
- NF S90-751:1990 MEDICO-SURGICAL EQUIPMENT. INTRA-OCULAR LENSES. GENERAL REQUIREMENTS FOR STERILIZATION,PACKAGING AND LABELLING.
- NF H00-204*NF EN 14375:2016 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing
- NF S92-013:1996 In vitro diagnostic systems. Transport packages for medical and biological specimens. Requirements, tests.
- NF EN ISO 15378:2018 Articles d'emballage primaire pour médicaments - Exigences particulières pour l'application de l'ISO 9001:2015 prenant en considération les Bonnes Pratiques de Fabrication (BPF)
- NF S93-200*NF EN ISO 15378:2018 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
- NF S90-438-1:1992 MEDICAL SURGICAL EQUIPMENT. GUIDELINES FOR CLEANING, PACKAGING AND STERILIZATION OF ORTHOPAEDIC IMPLANTS. PART 1 : METALLIC IMPLANTS.
Danish Standards Foundation, Foreign pharmaceutical packaging
- DS/EN 15823:2010 Packaging - Braille on packaging for medicinal products
- DS/ISO 17351:2013 Packaging - Braille on packaging for medicinal products
- DS/ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging
- DS/EN ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging (ISO 21976:2018)
- DS/CEN/TR 15753:2008 Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people
- DS/EN 14375:2006 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing
- DS/EN 14375:2004 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing
- DS/EN ISO 15378:2012 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)
Lithuanian Standards Office , Foreign pharmaceutical packaging
- LST EN 15823-2010 Packaging - Braille on packaging for medicinal products
- LST EN ISO 17351:2014 Packaging - Braille on packaging for medicinal products (ISO 17351:2013)
- LST EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
- LST EN 14375-2004 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing
- LST EN 14375-2004/AC-2006 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing
- LST CEN ISO/TS 16791:2020 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020)
- LST EN ISO 15378:2012 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP) (ISO 15378:2011)
German Institute for Standardization, Foreign pharmaceutical packaging
- DIN EN ISO 17351:2014-10 Packaging - Braille on packaging for medicinal products (ISO 17351:2013); German version EN ISO 17351:2014
- DIN EN ISO 21976:2020-12 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018); German version EN ISO 21976:2020
- DIN EN 16679:2015 Packaging - Tamper verification features for medicinal product packaging; German version EN 16679:2014
- DIN EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018); German version EN ISO 21976:2020
- DIN CEN ISO/TS 16791:2021-02 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020); German version CEN ISO/TS 16791:2020
- DIN EN ISO 15378:2018-04 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017); German version EN ISO 15378:2017
- DIN EN 14375 Corrigendum 1:2006 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing Corrigendum 1 to English version of DIN EN 14375:2004-02
- DIN EN ISO 15378:2018 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017)
- DIN EN ISO 11239:2022-10 Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (IS...
- DIN EN ISO 11239:2013-03 Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (IS...
- DIN EN ISO 11239:2023-10 Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (IS...
European Committee for Standardization (CEN), Foreign pharmaceutical packaging
- EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
- PD CEN/TR 15753:2008 Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people
- EN ISO/TS 16791:2015 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers
- EN 829:1996 In Vitro Diagnostic Systems - Transport Packages for Medical and Biological Specimens - Requirements, Tests
- prEN 829-1992 In vitro diagnostic systems; transport packages for medical and biological specimens; requirements; tests
- CEN ISO/TS 16791:2015 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2014)
- CEN ISO/TS 16791:2020 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020)
- EN ISO 15378:2011 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)
- EN 13795-2:2004 Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods Incorporates Amendment A1: 2009
- EN ISO 11239:2023 Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (IS...
IT-UNI, Foreign pharmaceutical packaging
- UNI EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging
- UNI CEN ISO/TS 16791:2020 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers
International Organization for Standardization (ISO), Foreign pharmaceutical packaging
- ISO 21976:2018 Packaging — Tamper verification features for medicinal product packaging
- ISO 18665:2015 Traditional Chinese medicine - Herbal decoction apparatus
- ISO/TS 16791:2014 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers
- ISO/TS 16791:2020 Health informatics — Requirements for international machine-readable coding of medicinal product package identifiers
- ISO 11239:2012 Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging
- ISO/PRF 11239 Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging
British Standards Institution (BSI), Foreign pharmaceutical packaging
- BS EN 16679:2014 Packaging. Tamper verification features for medicinal product packaging
- BS EN ISO 21976:2020 Packaging. Tamper verification features for medicinal product packaging
- BS ISO 18665:2015 Traditional Chinese medicine. Herbal decoction apparatus
- PD CEN ISO/TS 16791:2020 Health informatics. Requirements for international machine-readable coding of medicinal product package identifiers
- BS PD ISO/TS 16791:2014 Health informatics. Requirements for international machine-readable coding of medicinal product package identifiers
- BS EN ISO 15378:2015 Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)
- BS EN ISO 15378:2011 Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)
- 16/30347647 DC BS EN ISO 15378. Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
- BS EN ISO 15378:2017 Tracked Changes. Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
- BS EN ISO 11239:2023 Health informatics. Identification of medicinal products. Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging
AENOR, Foreign pharmaceutical packaging
- UNE-EN 16679:2015 Packaging - Tamper verification features for medicinal product packaging
- UNE-CEN/TR 15753:2009 IN Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people
Anhui Provincial Standard of the People's Republic of China, Foreign pharmaceutical packaging
- DB34/T 4136-2022 Work Specifications for Pharmaceutical R&D Outsourcing Services
CZ-CSN, Foreign pharmaceutical packaging
PT-IPQ, Foreign pharmaceutical packaging
- NP EN 862-2000 Packaging Child-resistant packaging Requirements and testing procedures for non-reclosable packages for non-pharmaceutical products
ES-UNE, Foreign pharmaceutical packaging
- UNE-EN ISO 21976:2021 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
- UNE-CEN ISO/TS 16791:2020 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020) (Endorsed by Asociación Española de Normalización in November of 2020.)
- UNE-EN ISO 15378:2018 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017)
ET-QSAE, Foreign pharmaceutical packaging
Inner Mongolia Provincial Standard of the People's Republic of China, Foreign pharmaceutical packaging
- DB15/T 1174-2017 Pharmaceutical logistics refrigerated drug transport packaging requirements
- DB15/T 962-2016 Main technical requirements for medical logistics sorting, conveying and packaging equipment
Military Standards (MIL-STD), Foreign pharmaceutical packaging
CH-SNV, Foreign pharmaceutical packaging
- SN EN ISO 21976:2021 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
PL-PKN, Foreign pharmaceutical packaging
RU-GOST R, Foreign pharmaceutical packaging
- GOST 17768-1990 Medicine remedies. Packing, marking, transportation and storage
- GOST R 57305-2016 Health informatics. Requirements for international machine-readable coding of medicinal product package identifiers
RO-ASRO, Foreign pharmaceutical packaging
- STAS 5598-1987 PRODUCTS OF OSIER WILLOW WATTLES Baskets for pharmaceutical products
U.S. Military Regulations and Norms, Foreign pharmaceutical packaging
- ARMY MIL-B-50856 A (3)-1990 BOXES, SET-UP PACKING, AMMUNITION INNER AND OUTER FOR SMALL EXPLOSIVE COMPONENTS
- ARMY MIL-B-50856 A-1975 BOXES, SET-UP PACKING, AMMUNITION INNER AND OUTER FOR SMALL EXPLOSIVE COMPONENTS
- ARMY MIL-DTL-3943/117 D VALID NOTICE 1-2013 Decoration, Surgeon General's Medallion, U.S. Public Health Service
- ARMY MIL-F-70518 (3)-1995 FLARE, INFRARED TRACKING, MARK 33 MOD 0 (ARMY) PARTS FOR AND LOADING, ASSEMBLING AND PACKING
- ARMY MIL-B-50856 A NOTICE 1-2013 BOXES, SET-UP, PACKING, AMMUNITION, INNER AND OUTER FOR SMALL EXPLOSIVES COMPONENTS
United States Navy, Foreign pharmaceutical packaging
- NAVY MIL-STD-1322 A NOTICE 3-1984 UNIT LOADS OF AMMUNITION AND EXPLOSIVES FOR DOMESTIC AND OVERSEAS SHIPMENT
- NAVY MIL-STD-1322 A NOTICE 2-1983 UNIT LOADS OF AMMUNITION AND EXPLOSIVES FOR DOMESTIC AND OVERSEAS SHIPMENT
- NAVY MIL-STD-1322 A NOTICE 1-1981 UNIT LOADS OF AMMUNITION AND EXPLOSIVES FOR DOMESTIC AND OVERSEAS SHIPMENT
- NAVY MIL-STD-1322 A-1981 UNIT LOADS OF AMMUNITION AND EXPLOSIVES FOR DOMESTIC AND OVERSEAS SHIPMENT
- NAVY MIL-STD-1322 A NOTICE 4-1986 UNIT LOADS OF AMMUNITION AND EXPLOSIVES FOR DOMESTIC AND OVERSEAS SHIPMENT
- NAVY MIL-STD-1322-815 NOTICE 1-1992 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT CUTTER, POWDER ACTUATED MK 23 MOD 0 OR CUTTER, POWDER ACTUATED MK 24 MOD 0 IN AMMUNITION BOX M2A1
- NAVY MIL-STD-1322-815-1986 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT CUTTER, POWDER ACTUATED MK 23 MOD 0 OR CUTTER, POWDER ACTUATED MK 24 MOD 0 IN AMMUNITION BOX M2A1
- NAVY MIL-STD-1322-806 NOTICE 2-1987 UNIT LOAD FOR DOMESTIC& OVERSEAS SHIPMENT CARTRIDGE, SIGNAL, PRACTICE BOMB MK 4 MOD 3 OR CXU-3 A/B IN BOX, AMMUNITION M2A1
- NAVY MIL-STD-1322-806 NOTICE 1-1982 UNIT LOAD FOR DOMESTIC& OVERSEAS SHIPMENT CARTRIDGE, SIGNAL, PRACTICE BOMB MK 4 MOD 3 OR CXU-3 A/B IN BOX, AMMUNITION M2A1
- NAVY MIL-STD-1322-806-1981 UNIT LOAD FOR DOMESTIC& OVERSEAS SHIPMENT CARTRIDGE, SIGNAL, PRACTICE BOMB MK 4 MOD 3 OR CXU-3 A/B IN BOX, AMMUNITION M2A1
- NAVY MIL-STD-1322/79 NOTICE 1-1999 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT SAFETY ARMING DEVICE ASSEMBLY, MK 75 IN AMMUNITION BOX M2A1
- NAVY MIL-STD-1322-114-1993 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT AN/SSQ-110 SONOBUOY (IN SONOBOUY LAUNCH CONTAINER) PACKED IN 36 UNIT BAYONET PALLET DL
- NAVY MIL-STD-1322/53 NOTICE 3-1999 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT PROPELLANT GRAIN MK 90 MOD 0 IN CONTAINER DWG 233AS171 PACKED IN PALLET CRATE MK 2 MOD 0
- NAVY MIL-STD-1322/53 VALID NOTICE 2-1991 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT PROPELLANT GRAIN MK 90 MOD 0 IN CONTAINER DWG 233AS171 PACKED IN PALLET CRATE MK 2 MOD 0
- NAVY MIL-STD-1322/53 VALID NOTICE 1-1984 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT PROPELLANT GRAIN MK 90 MOD 0 IN CONTAINER DWG 233AS171 PACKED IN PALLET CRATE MK 2 MOD 0
- NAVY MIL-STD-1322/53-1982 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT PROPELLANT GRAIN MK 90 MOD 0 IN CONTAINER DWG 233AS171 PACKED IN PALLET CRATE MK 2 MOD 0
- NAVY MIL-STD-1322-900-1993 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT PRIMER MK 22 MODS 0. 1. AND 2: PERCUSSION, FOR 40MM CARTRIDGE
- NAVY MIL-STD-1322-95 NOTICE 1-1993 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT CHARGE, DEMOLITION, MK 36 MOD 0 IN CONTAINER, DRAWING 10001-2511106
- NAVY MIL-STD-1322-95-1988 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT CHARGE, DEMOLITION, MK 36 MOD 0 IN CONTAINER, DRAWING 10001-2511106
- NAVY MIL-STD-1322-79-1985 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT SAFETY ARMING DEVICE ASSEMBLY, MK 75 IN AMMUNITION BOX M2A1
- NAVY MIL-STD-1322-61 NOTICE 4-1993 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT SLMM EXPLOSIVE SECTION MK 13 MOD 0 IN CONTAINER MK 639 MOD 0
- NAVY MIL-STD-1322-61-1984 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT SLMM EXPLOSIVE SECTION MK 13 MOD 0 IN CONTAINER MK 639 MOD 0
- NAVY MIL-STD-1322-64-1987 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT ARMING DEVICES MK 2 MODS AND MK 36 MOD 0 IN MK 2 MOD 0 AMMUNITION COMPONENT BOX
- NAVY MIL-STD-1322-73-1987 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT CARTRIDGE, CALIBER, .38 SPECIAL BALL, STEEL JACKETED WITH TRACER IN AMMUNITION BOX M2A1
- NAVY MIL-STD-1322-56 VALID NOTICE 1-1989 UNIT LOAD FOR DOMESTIC& OVERSEAS SHIPMENT WARHEAD MK 118 MOD 0 IN AMMO. COMPONENT BOX MK 2 MOD 0
- NAVY MIL-STD-1322-56-1982 UNIT LOAD FOR DOMESTIC& OVERSEAS SHIPMENT WARHEAD MK 118 MOD 0 IN AMMO. COMPONENT BOX MK 2 MOD 0
- NAVY MIL-STD-1322-67-1986 UNIT LOAD FOR DOMESTIC AND OVERSEAS SHIPMENT MK 136 MOD 0 ADAPTER IN SMALL ARMS AMMO BOX M2A1
Professional Standard - Agriculture, Foreign pharmaceutical packaging
- 303药典 四部-2020 4000 Testing methods for pharmaceutical packaging materials 4002 Determination of packaging materials by infrared spectroscopy
US-CFR-file, Foreign pharmaceutical packaging
- CFR 21-803.58-2014 Food and Drugs. Part803:Medical device reporting (Eff. 8-14-15). Section803.58:Foreign manufacturers.
- CFR 49-173.473-2014 Transportation. Part173:Shippers—general requirements for shipments and packagings. Section173.473:Requirements for foreign-made packages.
- CFR 21-801.128-2013 Food and Drugs. Part801:Labeling. Section801.128:Exceptions or alternatives to labeling requirements for medical devices held by the Strategic National Stockpile.
American Society for Testing and Materials (ASTM), Foreign pharmaceutical packaging
- ASTM D4775/D4775M-09 Standard Specification for Identification and Configuration of Prefilled Syringes and Delivery Systems for Drugs (Excluding Pharmacy Bulk Packages)
- ASTM F1886/F1886M-09 Standard Test Method for Determining Integrity of Seals for Medical Packaging by Visual Inspection
- ASTM D4775-94(1999) Standard Specification for Identification and Configuration of Prefilled Syringes and Delivery Systems for Drugs (Excluding Pharmacy Bulk Packages)
- ASTM D4775/D4775M-09(2014) Standard Specification for Identification and Configuration of Prefilled Syringes and Delivery Systems for Drugs (Excluding Pharmacy Bulk Packages)
- ASTM D4775-04 Standard Specification for Identification and Configuration of Prefilled Syringes and Delivery Systems for Drugs (Excluding Pharmacy Bulk Packages)
AT-ON, Foreign pharmaceutical packaging
- ONORM EN 829-1996 In vitro diagnostic systems-Transport packages for medical and biological specimens-Requirements,test
- ONR CEN ISO/TS 16791:2021 Health informatics - Requirements for international machine-readable coding of medicinal product package identifiers (ISO/TS 16791:2020)
未注明发布机构, Foreign pharmaceutical packaging
- BS EN 829:1997 In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements , tests
Korean Agency for Technology and Standards (KATS), Foreign pharmaceutical packaging
- KS J 0021-2010 Packaging and labelling system policy in biopharmaceutical production based on Good Manufacturing Practice
- KS X ISO 11239:2018 Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of pres
Group Standards of the People's Republic of China, Foreign pharmaceutical packaging
- T/CAAMM 2.3-2017 Tractor Products—Requirements for marking, packaging, transportation and storage—Part 3:Foreign sales of tractors
CEN - European Committee for Standardization, Foreign pharmaceutical packaging
- EN ISO 15378:2007 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2000@ with reference to Good Manufacturing Practice (GMP)
- EN ISO 15378:2017 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015@ with reference to good manufacturing practice (GMP)
KR-KS, Foreign pharmaceutical packaging
- KS X ISO 11239-2018 Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of pres
- KS X ISO 11239-2018(2023) Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of pres