Speaker Profile
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Chaitanya Baliga

Healthcare Quality and Regulatory Compliance

Dr. Chaitanya Baliga has over 20 years of experience in quality management systems, regulatory compliance, and supplier management in industries, such as consumer products, medical device, pharmaceuticals, automotive, and toys. One of Chaitanya’s responsibilities is ensuring quality and compliance activities pertaining to manufacturing of regulated products (drugs, natural health products, cosmetics, and medical devices).

Live Webinars

11
December,  2025
$119.00

Risk Based Supplier Evaluation

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
09
December,  2025
$345.00

4-Hour Virtual Seminar on Overview of Hazard Analysis and Risk Analys ...

  • 10:00 AM PST | 01:00 PM EST
  • 4 Hours
  •  Details
04
December,  2025
$345.00

4-Hour Virtual Seminar on Supplier Qualification: Risk-Based Supplier ...

  • 10:00 AM PST | 01:00 PM EST
  • 4 Hours
  •  Details
02
December,  2025
$119.00

Risk Assessment in Software Development Process

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
20
November,  2025
$119.00

Root Cause Analysis in Regulated Industry - Tools and Approach to Ens ...

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
19
November,  2025
$119.00

Lean and Six Sigma Methods to Drive Continual Improvement in Process

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
18
November,  2025
$119.00

Hazard Identification and Risk Assessment, and Tools to Assess Risk

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
13
November,  2025
$119.00

Commercialization Drug Device Combination Product

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
11
November,  2025
$119.00

Understanding the Requirements of the International MDSAP Audit Appro ...

  • 10:00 AM PST | 01:00 PM EST
  • 60 Minutes
  •  Details
06
November,  2025
$345.00

4-Hour Virtual Seminar on Risk Management Training with DFMEA and PFM ...

  • 10:00 AM PST | 01:00 PM EST
  • 4 Hours
  •  Details
16
October,  2025
$119.00

Understanding and Implementing a Quality by Design (QbD) Pr ...

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
14
October,  2025
$345.00

4-Hour Virtual Seminar on CAPA & Root Cause Investigation for Med ...

  • 10:00 AM PDT | 01:00 PM EDT
  • 4 Hours
  •  Details
09
October,  2025
$119.00

Process Failure Mode and Effects Analysis (PFMEA)

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
07
October,  2025
$119.00

Good Documentation Practices GDP 101

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
02
October,  2025
$119.00

Quality by Design (QbD) in Pharmaceutical Development

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
25
September,  2025
$119.00

Quality By Design (QbD), A Method for Medicinal Product Dev ...

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
17
September,  2025
$119.00

Risk Based Supplier Evaluation

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details
16
September,  2025
$345.00

4-Hour Virtual Seminar on Overview of Hazard Analysis and Risk Analys ...

  • 10:00 AM PDT | 01:00 PM EDT
  • 4 Hours
  •  Details
10
September,  2025
$345.00

4-Hour Virtual Seminar on Supplier Qualification: Risk-Based Supplier ...

  • 10:00 AM PDT | 01:00 PM EDT
  • 4 Hours
  •  Details
09
September,  2025
$119.00

Risk Assessment in Software Development Process

  • 10:00 AM PDT | 01:00 PM EDT
  • 60 Minutes
  •  Details

Recorded Webinars

Risk Based Supplier Evaluation

Risk Based Supplier Evaluation

Risk Based Supplier Evaluation