Statistical Evaluation – Crossing the Process Capability in Pharma

Online Live Training

Statistical Evaluation – Crossing the Process Capability in Pharma

24th Oct 2020 | 10 AM IST | 2 Hours


Course Expert

Mr. Hitendrakumar Shah

A Quality-oriented professional with over 2 decades of experience in Quality Assurance, Quality Control, Quality Engineering, Quality auditor, pharmaceutical regulations, and regulatory audit compliance. The area of expertise is as per the requirement of USFDA, EUGMP, PICS, MHRA, TGA, TPD, ANVISA, WHO, and Schedule-M Guidelines.

Introduction:

As, we are approaching to end of this calendar year and welcome new year. All pharmaceutical industries will now put focus on Product quality review preparation and calculating the process capabilities.

However, now the time has come where we need to see beyond the process capability. We need to focus on use of Statistical evaluation for process control systems. It is just a one step ahead approach for compliance. That is what we speak about cGMP. As a part of continuous improvement in the quality system, this “Statistical Evaluation” will really play a very important role to upgrade and improve the process and further helping to improve the product quality.


Who Should ATTEND?

This Training Course will benefit all who are working in pharmaceutical industries. Those who are auditors, participating in validation, quality control, production, compliance and ensure process and product improvement etc.

  • QA/ QC
  • Regulatory Affairs
  • Project Managers
  • Validation personnel
  • Compliance personnel
  • Auditors Personnel involved in QMS

Register Now

Course Investment: INR 1200/-
To confirm your position, Contact now
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For Registration

Utsav Sahani – Head Registrations

[email protected] | +91 93214 97158