MASTERCLASS
Effective Investigations
for Ensuring Quality and Compliance
28th April (Sunday) | 11 AM – 01 PM
Registrations Closed!
What Will You Learn?
Learn how to conduct efficient and timely quality investigations in the pharmaceutical industry.
Who Should Attend?
This webinar is a must-attend for employees working in GMP-regulated areas like manufacturing, QC, QA, and technical services.
Why Should You Attend
- You’ll gain valuable insights into the regulatory expectations and responsibilities associated with investigations.
- This includes the classification of deviations, root cause analysis, planning immediate measures, and making informed decisions.
- Attending this webinar will enhance your investigative skills and ensure that you can effectively address quality issues while complying with industry standards.
Learning Flow
FIRST HALF
1. Introduction to Quality Investigations:
-Importance in the pharmaceutical industry.
-Regulatory requirements overview.
2. Roles and Responsibilities:
-Investigator qualifications and duties.
3. Classification of Deviations:
-Severity levels and implications.
SECOND HALF
1. Root Cause Analysis (RCA):
-Various RCA methodologies.
-Practical application.
2. Planning and Execution:
-Developing investigation plans.
-Implementing corrective actions.
3. Decision-Making and Reporting:
-Process guidelines.
-Documentation and reporting requirements.
Educator
Enroll in an exclusive learning experience led by the Pharma industry's top-tier
professionals and gain an unparalleled competitive edge.
Dr. Sanjit Singh Lamba
Managing Partner
Trillyum Consulting and Advisory
Event Registration Form
Will I get the certificate?
Certificate to be awarded by PharmaState Academy in collaboration with Trillyum Consulting with 3CPhE (Continuing Pharma Education) points. Registration is mandatory for certification.
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Continuing Pharma Education – An Initiative by your L&D Partner PharmaState Academy.
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