ASTM E2475 - 10(2016) - Standard Guide for Process Understanding Related to Pharmaceutical Manufacture and Control

ASTM E2475 - 10(2016)

Standard Guide for Process Understanding Related to Pharmaceutical Manufacture and Control

Status : Current   Published : September 2016

Format
PDF

Format
HARDCOPY



1.1 The purpose of this guide is to establish a framework and context for process understanding for pharmaceutical manufacturing using quality by design (QbD) (Juran, 1992; 2 FDA/ICH Q8). The framework is applicable to both active pharmaceutical ingredient (API) and to drug product (DP) manufacturing. High (detailed) level process understanding can be used to facilitate production of product which consistently meets required specifications. It can also play a key role in continuous process improvement efforts.

1.2 Process Analytical Technology (PAT) is one element that can be used for achieving control over those inputs determined to be critical to a process. It is important for the reader to recognize that PAT is defined as:

[This table has been removed.]

1.3  This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.




Standard NumberASTM E2475 - 10(2016)
TitleStandard Guide for Process Understanding Related to Pharmaceutical Manufacture and Control
StatusCurrent
Publication Date01 September 2016
Normative References(Required to achieve compliance to this standard)No other standards are normatively referenced
Informative References(Provided for Information)No other standards are informatively referenced
Descriptors Control, Pharmaceutical manufacture, Process understanding
ICS11.120.01
PublisherASTM
FormatA4
DeliveryYes
Pages7
File Size151 KB
Price£40.00


 Your basket
Your basket is empty

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


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


Tracked Changes

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