15/30315528 DC : 0
|
BS ISO 4802-2 - GLASSWARE - HYDROLYTIC RESISTANCE OF THE INTERIOR SURFACES OF GLASS CONTAINERS - PART 2: DETERMINATION BY FLAME SPECTROMETRY AND CLASSIFICATION |
09/30178946 DC : 0
|
BS ISO 4802-1 - GLASSWARE - HYDROLYTIC RESISTANCE OF THE INTERIOR SURFACES OF GLASS CONTAINERS - PART 1: DETERMINATION BY TITRATION METHOD AND CLASSIFICATION |
09/30178949 DC : 0
|
BS ISO 4802-2 - GLASSWARE - HYDROLYTIC RESISTANCE OF THE INTERIOR SURFACES OF GLASS CONTAINERS - PART 2: DETERMINATION BY FLAME SPECTROMETRY AND CLASSIFICATION |
BS ISO 4802-1:2016
|
Glassware. Hydrolytic resistance of the interior surfaces of glass containers Determination by titration method and classification |
ISO 4802-1:2016
|
Glassware — Hydrolytic resistance of the interior surfaces of glass containers — Part 1: Determination by titration method and classification |
I.S. EN ISO 8871-5:2016
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
ISO 8871-5:2016
|
Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing |
DIN ISO 10985:2009-12
|
Caps made of aluminium-plastics combinations for infusion bottles and injection vials - Requirements and test methods (ISO 10985:2009) |
DIN EN ISO 8871-5 E : 2017
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
BS ISO 4802-2:2016
|
Glassware. Hydrolytic resistance of the interior surfaces of glass containers Determination by flame spectrometry and classification |
BS EN ISO 8362-7:2010
|
Injection containers and accessories Injection caps made of aluminium-plastics combinations without overlapping plastics part |
15/30324254 DC : 0
|
BS EN ISO 8871-5 - ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING |
UNE-EN ISO 8362-7:2011
|
Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part (ISO 8362-7:2006) |
BS EN ISO 7864:2016
|
Sterile hypodermic needles for single use. Requirements and test methods |
DIN ISO 8362-7:2007-06
|
INJECTION CONTAINERS AND ACCESSORIES - PART 7: INJECTION CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS WITHOUT OVERLAPPING PLASTICS PART |
I.S. EN ISO 7864:2016
|
STERILE HYPODERMIC NEEDLES FOR SINGLE USE - REQUIREMENTS AND TEST METHODS (ISO/DIS 7864:2014) |
DIN ISO 10985 E : 2009
|
CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS FOR INFUSION BOTTLES AND INJECTION VIALS - REQUIREMENTS AND TEST METHODS |
UNI EN ISO 8362-7 : 2011
|
INJECTION CONTAINERS AND ACCESSORIES - PART 7: INJECTION CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS WITHOUT OVERLAPPING PLASTICS PART |
DIN EN ISO 8362-2:2016-02
|
Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2015) |
03/115519 DC : 0
|
BS ISO 15137 - SELF-ADHESIVE HANGING DEVICES FOR INFUSION BOTTLES AND INJECTION VIALS - REQUIREMENTS AND TEST METHODS |
EN ISO 8362-2:2015
|
Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2015) |
14/30296389 DC : 0
|
BS EN ISO 7864 - STERILE HYPODERMIC NEEDLES FOR SINGLE USE - REQUIREMENTS AND TEST METHODS |
04/30086336 DC : 0
|
BS ISO 8871-5 - ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING |
BS EN ISO 8871-5:2016
|
Elastomeric parts for parenterals and for devices for pharmaceutical use Functional requirements and testing |
BS EN ISO 8362-2:2015
|
Injection containers and accessories Closures for injection vials |
NF EN ISO 8362-7 : 2011
|
INJECTION CONTAINERS AND ACCESSORIES - PART 7: INJECTION CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS WITHOUT OVERLAPPING PLASTICS PART |
I.S. EN ISO 8362-7:2010
|
INJECTION CONTAINERS AND ACCESSORIES - PART 7: INJECTION CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS WITHOUT OVERLAPPING PLASTICS PART |
ISO 4802-2:2016
|
Glassware — Hydrolytic resistance of the interior surfaces of glass containers — Part 2: Determination by flame spectrometry and classification |
I.S. EN ISO 8362-2:2015
|
INJECTION CONTAINERS AND ACCESSORIES - PART 2: CLOSURES FOR INJECTION VIALS (ISO 8362-2:2015) |
ISO 7864:2016
|
Sterile hypodermic needles for single use — Requirements and test methods |
ISO 8362-2:2015
|
Injection containers and accessories — Part 2: Closures for injection vials |
UNE-EN ISO 7864:2017
|
Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016) |
EN ISO 8871-5:2016
|
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016) |
EN ISO 7864:2016
|
Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016) |
EN ISO 8362-7:2010
|
Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part (ISO 8362-7:2006) |
DIN EN ISO 8362-7:2011-03
|
Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part (ISO 8362-7:2006) |
15/30315525 DC : 0
|
BS ISO 4802-1 - GLASSWARE - HYDROLYTIC RESISTANCE OF THE INTERIOR SURFACES OF GLASS CONTAINERS - PART 1: DETERMINATION BY TITRATION METHOD AND CLASSIFICATION |
UNE-EN ISO 8871-5:2017
|
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016) |
DIN EN ISO 8871-5:2015-08 (Draft)
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |
09/30196282 DC : DRAFT AUG 2009
|
BS ISO 8362-6 - INJECTION CONTAINERS AND ACCESSORIES - PART 6: CAPS MADE OF ALUMINIUM-PLASTICS COMBINATIONS FOR INJECTION VIALS |
ISO 10985:2009
|
Caps made of aluminium-plastics combinations for infusion bottles and injection vials — Requirements and test methods |
DIN EN ISO 8871-5:2017-03
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 5: FUNCTIONAL REQUIREMENTS AND TESTING (ISO 8871-5:2016) |