Faculty: Saurabh Joshi


  • Date: 6/29/2022 11:00 AM - 6/29/2022 12:00 PM
  • Location: Online Event

Tickets


Ticket Type
Qty
Live- Single
$200.00
0
For ONE Participant – Live session only
Live Corporate
$700.00
0
For Maximum of 10 participants – Live session only
Recording - Single
$350.00
0
Recording access for ONE participant (viewer) – Unlimited viewing access for 6 months
Recording - Corporate
$1400.00
0
Recording access (Multiple licenses) for up to 10 participants – Unlimited viewing access for 6 months

Total

$0.00

Description

Equipment qualification and process validation is a cumbersome activity if realistic but compliant approach is not applied. This session should help responsible personnel and teams to apply efforts in right direction to ensure regulator satisfaction at the same time help company operationalize full potential of both process and equipment/system.

Lack of adequate qualification or validation is a common FDA inspectional observation and FDA Warning Letter violation. Those involved in equipment qualification, manufacturing and process validation will benefit from a review of the relevant FDA rules, written and unwritten. Those involved in hosting FDA inspections will also benefit.

Areas Covered in the Session :

  • Qualification vs. Validation vs. Verification
  • Process Validation vs. Equipment Qualification
  • Stages of Process Validation (practical approach in FDAs framework)
  • Specifications, When to test, What to test, How much to test
  • Elements of Protocols (IQ, OQ, PQ)
  • Deliverables
  • Role of QMS

Who Should Attend:

  • Quality Assurance Departments
  • Validation and Qualification Teams
  • Engineering Departments
  • Manufacturing Departments
  • Operations Departments
  • Maintenance Teams
  • Every Personnel responsible for Qualification of Equipment and Validation of Processes

Speaker: SAURABH JOSHI

Saurabh Joshi is founder of StepUP Consultants, a pharmaceutical operations consulting company. He is renown for his contributions in executing robotics and automation projects for industry 4.0 transformation.

An industry professional with over 20 years hands on experience in Quality operations, Quality systems, Tech. transfer, Compliance, Validation and Qualifications; has successfully lead numerous regulatory inspections from USFDA, MHRA, WHO GMP (Geneva), HPRA for reputed organizations he has been a part of, such as, Cipla, Microlabs, Wockhardt, Sun Pharma to name a few. He has been an external Quality consultant with Merck specialties Pvt. Ltd. (A Merck KGaA, Darmstadt Germany company) guiding from shop floor at site to leading corporate level functions.

His consulting expertise includes, gap assessments and SOP preparation, regulatory inspections, QMS, technology transfer, Process Validation and equipment qualification, GMP, Data Integrity and Artificial Intelligence & Robotics.