ncvet-help[at]gov[dot]in
Beta Version
+91 11 25788001-11

Life Sciences GMP: Deviation special Investigation & Reporting

NQR Code:NM-06-LS-04439-2025-V2-LSSSDC

  • Old Code: NM-06-LS-04439-2025-V2-LSSSDC

    Copy
About this Qualification

Job Description

The Deviation special Investigation & Reporting Program equips life sciences professionals with competency in handling Out-of-Specification (OOS) results and conducting thorough, regulatory-compliant investigations in pharmaceutical and life sciences manufacturing. Learners will be trained on regulatory expectations, stepwise investigation procedures, common pitfalls, and documentation best practices. In addition, the program emphasizes the role of Corrective and Preventive Actions (CAPA) and continuous improvement practices to avoid recurrence. Practical exercises, case studies, and peer reviews ensure participants gain hands-on experience in drafting investigation reports and implementing CAPA plans.

Eligibility Criteria

Criteria 1 Criteria 2 Experience Training Qualification
3 year UG degree In any field 2 years None
Pursuing 4th year of 3-year/ 4-years UG In relevant field No Experience None

Progression Pathway

  • Not Available

Learning Module In Job Role/Qualifcation

National Occupation Standards (NOS)/Module NOS Code Mandatory/ Optional Estimated size (Hours) Nos Credit Level
Life Sciences GMP: Deviation special Investigation & Reporting LFS/MCr-0026, V1 Mandatory 15 0.5 6