ICH guideline

ICH Q2(R2)/Q14: Training on Validation of Analytical Procedures and Q14: Analytical Procedure Development

ICH guideline · Quality Guidelines

Key facts

ICH code Q2(R2)/Q14
Title Training on Validation of Analytical Procedures and Q14: Analytical Procedure Development
Guideline series Quality Guidelines
ICH summary (excerpt) Further to the ICH Management Committee’s endorsement of the Q2(R2)/Q14 IWG Concept Paper in October 2023, the Q2(R2)/Q14 IWG was established to prepare and deliver training materials which will facilitate an aligned interpretation and a harmonised implementation of Q2(R2) “Validation of Analytical” Procedures and Q14…
File Q2(R2)/Q14 Training Material Module 7
File type PDF
File on ich.org database.ich.org

At a glance

  • Yes Full text searchable in Orca1
  • Q2(R2)/Q14 Training Material Module 7 Files published by ICH
  • None FDA guidance documents based on this guideline

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About ICH guidelines

ICH guidelines harmonise the technical requirements for registering medicines in the ICH regions. Each guideline moves through a five-step process, from concept paper to adoption and implementation by regulators.

Source: International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). Guideline summaries are ICH material, reproduced with acknowledgement

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