2-Hour Virtual Seminar on Data Integrity in Microbiology Laboratories

The training program is tailored to specific departments, including reviewers, supervisors, managers, and management, to ensure data integrity in Microbiology Laboratories.
  • Wednesday
  • June
  • 24
  • 2026
08:00 AM PDT | 11:00 AM EDT
Duration: 2 Hours
IMG Hitendrakumar Shah
Webinar Id: 62311
Live
Session
$149.00
Single Attendee
$299.00
Group Attendees
Recorded
Session
$199.00
Single Attendee
$399.00
Group Attendees
Combo
Live+Recorded
$299.00
Single Attendee
$599.00
Group Attendees

Overview:

In microbiology laboratories, most of all activities like testing and documentation are manual so chances of data integrity are very high due to very high human interventions.

Data Integrity is currently the major concern with both the FDA and European Regulatory Agencies. Many FDA warning letters and EU GMP inspections have highlighted major data integrity failures at companies globally. 

The training on data integrity should be different for different departments, further reviewers should have specific training, supervisors and managers should have specific training and the management should have specific training.

Due to this, the training program is designed for the  personnel working in Microbiology Laboratories.

Why should you Attend:

The learning objectives are firstly understanding the data integrity requirements in Pharmaceutical organisations specifically in microbiology laboratories

How Laboratory personnel can ensure compliance and be able to defend their positions. 

The benefits are, 

  • The person’s understanding about data integrity will be clear
  • The person working in production will become vigilant while generating and handling the data
  • The data integrity awareness will be increase in the company

Areas Covered in the Session:

  • Different guidelines on Data Integrity
  • Evaluation of FDA warning letter and  assessment
  • Understanding ALCOA+ concept
  • Common examples of data integrity
  • Audit Trail in microbiology 
  • Sterility Test - When we can repeat
  • Q&A 
  • Vote of Thanks and contact details

Who Will Benefit:

  • Quality Assurance
  • Quality Control
  • Pharmaceutical IT compliance
  • Global QA
  • corporate QA and QC
  • IT Personnel working or related to Pharma IT Support

Speaker Profile

Hitendrakumar Shah is a Quality oriented professional with over 23 years 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 & Schedule-M Guidelines. The key competencies include, Quality Compliance, Supplier Audit, build systems to encourage compliance with the principles of data integrity, computer system validation, Training, Risk assessment, Facing the audits, preparation and review of audit compliance, Qualification & validation, system development for CAPA effectiveness, stability studies & solving preapproval or post approval queries raised by regulatory agencies etc.

Independently handled - Quality assurance and Quality Control department for more than 13 years.

Audits faced- USFDA (8 times), ANVISA, MHRA, MCC, TGA,IDMA excellence, WHO audit, EU regulatory (9 times) , Yemen MOH, Digemid (Peru), Russian Authority audit etc.

Analytical Background: The analytical background includes, physical, chemical, microbiological testing of raw material, finished product & Stability samples. Handled the chromatographic instruments - HPLC, GC, FTIR, UV Visible spectrophotometer, AAS etc.