Statistics in Pharmaceutical Quality Control

Instructor: Yara Almouti 
Product ID: 702120
  • Duration: 90 Min

recorded version

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Last Recorded Date: May-2012

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Read Frequently Asked Questions

This 90-minute training on statistics used in pharmaceutical quality control will cover statistical interpretation related to quality control test results and process indicators in the pharmaceutical industry.

Why Should You Attend:

Quality control tests in pharmaceutical industry carries a burden on its own, as these tests are usually complicated, time consuming and expensive, and in many cases wrong interpretation of test results lead to disastrous situations. Any QC test is not considered successful until the resulting data are analyzed statistically and are complied within specifications limits. Wrong interpretation of the tests results can cost the company since it can end with a perfectly good batch being rejected.

Statistics in QC is a crucial element in deciding the acceptance or rejection of a product. Statistical interpretation of the test results is key to the complete understanding of tests results and criteria, and statistics based sampling plans is key to a comprehensive and efficient sampling system.

This informative webinar will qualify the attendee as a Quality Control professional and will cover all about statistical interpretation related to Quality Control test results and process indicators in the pharmaceutical industry.

Areas Covered in the Seminar:

  • Quality Statistical Terminology and Equations.
  • Type of errors.
  • Control Charts.
  • Interpretation of control charts.
  • Process capability.
  • Acceptance sampling.
  • Sampling plans.
  • Case study.

Who Will Benefit:

This webinar will provide valuable assistance to the following personnel in pharmaceutical manufacturing companies:

  • Quality Control Managers/ Employees
  • Quality Assurance Managers/Employees
  • Inspectors in the pharmaceutical field
  • Internal Quality Auditors in the manufacturers companies

Instructor Profile:

Yara Al-Mouti, is a passionate Quality and Process Optimization Specialist. In the last 14 years, she has successfully managed several compliance projects for a number of Pharmaceutical Manufacturers and obtained GMP certifications from regulatory agencies in the EU and GCC. In addition, she has managed GSDP compliance projects for number of drug stores. She is an expert in delivering Gap Assessment and Diagnosis projects that provide detailed Quality systems diagnosis reports and task plans.

Ms. Yara has been involved in setting up of turnkey pharmaceutical manufacturing facilities, from early design phases, equipment\contractors selection and purchasing, installation, commissioning and validation. She has successfully conducted a number of training workshops and conferences, developed building capacity programs for pharmaceutical manufacturers and their employees.

Ms. Yara has a degree in Chemical Engineering.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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