• PDA TR 61

PDA TR 61

  • Technical Report No. 61 (TR 61) Steam In Place
  • Report / Survey by Parenteral Drug Association, 03/01/2013
  • Category: PDA

$325.00 $163.00

This technical report complements PDA Technical Report No. 1 (Revised 2007): Validation of Moist Heat Sterilization Processes: Cycle Design, Development, Qualification and Ongoing Control with a focus on steam-in-place (SIP) processes. The primary objective of the task force responsible for this technical report was to develop a scientific technical report on SIP processes that provides recommendations for use by industry and regulators. References to appropriate and up-to-date scientific publications, international regulatory documents, journal articles, technical papers, and books are used to provide more detail and supportive data can be found. This document focuses on the various applications of steam for in situ sterilization for "sterile" applications and for in situ sanitization and other bioburden control applications widely used for systems that do not claim to be "sterilized" via steam. Risk management employed throughout the lifecycle of SIP equipment and processes to efficiently focus and allocate resources commensurate with the probability of impacting final product purity and safety is also covered. The task force was composed of European, North American, and South American industry professionals to ensure the methods, terminology, and practices of SIP reflect sound science and can be applied globally. This technical report was disseminated for public review and comment prior to publication, to provide the widest possible review and ensure its suitability as a guide to industry.
PDF

All of our standards document are available in PDF (Portable Document Format), an electronic, downloadable format.You will be able to download the file in your account downloads.

Multi-User Access

After purchasing, you have the ability to assign each license to a specific user.

Printable

At any time, you are permitted to make printed copies for your and your members' reference use.

PDA TR 76

PDA TR 76

Technical Report No. 76 (TR 76) Identification and Classification of Visible Nonconformities in Elas..

$163.00 $325.00

PDA TR 56

PDA TR 56

Technical Report No. 56 Revised 2016 (TR 56) Application of Phase-Appropriate Quality System and cGM..

$163.00 $325.00

PDA TR 77

PDA TR 77

Technical Report No. 77 (TR 77) The Manufacture of Sterile Pharmaceutical Products Using Blow-Fill-S..

$163.00 $325.00

PDA TR 60-2

PDA TR 60-2

Technical Report No. 60-2 (TR 60-2) Process Validation: A Lifecycle Approach, Annex 1: Oral Solid Do..

$163.00 $325.00