EQUIPMENT VALIDATION / QUALIFICATION (IQ,OP & PQ)

CERTIFICATE TRAINING


Live Session

Certificate Awarded: Equipment Validation/ Qualification (IQ, OP & PQ)- Certificate

Time: 9.30 AM – 4.30 PM

Level of Training: Beginners | Intermediate

Mode of Delivery: Live Interactive Instructor-led Webinar

Date: May 29, 2021

Fee: $960

(Contact us for the Recorded webinar)

Webinar Overview

● A system needs to be fully qualified to produce high-quality products in a consistent manner. Therefore Equipment Validation is of utmost importance. Equipment Validation comprises a series of system qualifications, such as Design, Installation, Operational, and Performance Qualification, that provide a high degree of assurance of the consistent, expected functioning of equipment.

● This webinar on equipment validation in the pharmaceutical industry focuses on Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) or Continuous Qualification (CQ), Qualification Protocol Test Case Examples, Power off / Power failure tests, Door Open tests, Alarm testing, Loaded and Empty Mappings, Instrument/equipment calibration.

● Aspirants who want to become Equipment Validation Specialist, Validation Engineer or Specialist, Process Engineer or Project Engineer, Quality Assurance Specialist, Quality Control Specialist, Maintenance Engineer, Maintenance Technician, Senior Validation Manager should attend this webinar on equipment validation in the pharmaceutical industry.

Course Offers

Register for 3 webinars at NACPT and get any available 1-day certificate training for free.

Equipment Validation/ Qualification (IQ, OP & PQ)

  • Module 1
  • ● Guidelines and Standards
  • ● Installation Qualification (IQ)
  • ● Operational Qualification (OQ)
  • Module 2
  • ● Performance Qualification (PQ) or Continuous Qualification (CQ)
  • ● Qualification Protocol Test Case Examples
  • Module 3
  • ● Power off / Power failure tests
  • ● Door Open tests
  • ● Temperature Distribution tests
  • ● Temperature Penetration tests
  • Module 4
  • ● Alarm testing
  • ● Loaded and Empty Mappings
  • ● Instrument / Equipment calibration
  • Module 5
  • ● Shelf mapping, vacuum testing, biological indicator test, Bowie Dick test, vacuum leak test, conductivity tests, riboflavin removal testing, controlled rate mapping
  • ● Qualification and Validation Service Reports, Protocols and SOPs
  • After successful completion of this course, students will be :
  • ● Able to understand current good clinical practices
  • ● Able to organize clinical studies
  • ● Able to coordinate clinical studies
  • ● Able to write procedures and protocols
  • ● Able to perform audit and inspections
  • ● Validation Assistant
  • ● Validation Specialists
  • ● Coordinators
  • ● Managers
  • Anyone who wants to become the following should attend this webinar on equipment validation in the pharmaceutical industry.
  • ● Validation Specialist
  • ● Validation Engineer or Specialist
  • ● Process Engineer or Project Engineer
  • ● Quality Assurance Specialist
    ● Quality Control Specialist
    ● Maintenance Engineer
    ● Maintenance Technician
    ● Senior Validation Manager

Equipment Validation | Equipment Qualification | Equipment Validation Training | Validation of Equipment Pharmaceutical | Equipment Validation in Pharmaceutical Industry | Requalification of Equipment Pharmaceutical | Pq Certificate | Performance Qualification Pharmaceutical Equipment

 

Dean Rathi Param

B.Sc., Post Grad Cert., in Pharma QA QC, (MBA/TECH)

 

She is an innovative and creative leader with more than twelve years of hands-on experience in many scientific industries, complemented with ten years of training/teaching experience.

 

Rathi Param is the president/founder of the North American College of Pharmaceutical Technology (NACPT) and ValidationTech Inc. She is an innovative and creative leader with more than twelve years of hands-on experience in many scientific industries (medical devices, environmental, food, pharmaceutical and biopharmaceutical), complemented with ten years of training/teaching experience. She possesses extensive expertise and knowledge of Quality Control, Quality Assurance, Validation, Technology Transfer, Manufacturing Technology, Process Improvements, Auditing and Inspection.

 

In the past twelve years, Rathi has held strategic management roles in major Canadian name brand/generic pharmaceutical companies. Validation Scientist at Patheon Inc., Validation Services Manager at Sanofi Pasteur Limited, Toronto., Validation Specialist at CibaVision, Toronto., and Validation Quality Engineer (Consultant) at iPOC, Toronto were few to be named.

 

Her interest in helping graduates to commence their careers in the pharmaceutical industry was the motivation to launch NACPT and Validation Tech, to provide hands-on training and create a platform to direct the pathway to successful recruitments by the pharmaceutical companies.

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