15/30319977 DC - BS ISO/IEC 13818-1. Information technology. Generic coding of moving pictures and associated audio information. Part 1. Systems

15/30319977 DC

BS ISO/IEC 13818-1. Information technology. Generic coding of moving pictures and associated audio information. Part 1. Systems

Status : Current, Draft for public comment   Published : April 2015

Format
PDF

Format
HARDCOPY






Standard Number15/30319977 DC
TitleBS ISO/IEC 13818-1. Information technology. Generic coding of moving pictures and associated audio information. Part 1. Systems
StatusCurrent, Draft for public comment
Publication Date23 April 2015
Normative References(Required to achieve compliance to this standard)ITU-T H.262:2000, ISO/IEC 13818-2:2000, ITU-T H.264:2013, ISO/IEC 14496-10:2013, ITU-T H.265:2013, ISO/IEC 23008-2:2013, ITU-T T.171:1996, ISO/IEC 13522-1:1997, ITU-T J.17:1988, ITU-T T.800:2002, ISO/IEC 15444-1:2004, ITU-R BT.470-7:2005, ITU-R BT.601-6:2007, ITU-R BR.648, ISO 639-2:1998, ISO 8859-1:1998, ISO 15706:2002, ISO/IEC 11172-1:1993, ISO/IEC 11172-2:1993, ISO/IEC 11172-3:1993, ISO/IEC 13818-3:1998, ISO/IEC 13818-6:1998, ISO/IEC 13818-7:2006, ISO/IEC 13818-11:2004, ISO/IEC 14496-1:2010, ISO/IEC 14496-2:2004, ISO/IEC 14496-3:2009, ISO/IEC 14496-17:2006, ISO/IEC 23009-1:2014, ISO/PRF 15706-2, IEC 60908:1999
Informative References(Provided for Information)IETF RFC 6381:2011, IETF RFC 3550:2003, ISO/IEC 14496-18:2004
International RelationshipsISO/IEC DIS 13818-1:2015
Draft Expiry Date23 June 2015
DescriptorsData processing, Information exchange, Coding (data conversion), Information systems, Digital recording methods, Video recording, Sound recording, Acoustic signals, Video signals, Cinematography, Digital signals, Data transmission, Data conversion, Decoding, Data blocks, Syntax, Semantics, Data layout, Definitions, Systemology
ICS35.040.40
CommitteeIST/37
PublisherBSI
FormatA4
DeliveryYes
Pages252
File Size2.615 MB
NotesWarning: this draft is not current beyond its expiry date for comments.
Price£66.00


 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents


Tracked Changes

Understand the changes made to a standard with our new Tracked Changes version


Develop a PAS

Develop a fast-track standardization document in 9-12 months


Worldwide Standards
We can source any standard from anywhere in the world