ComplianceOnline

Statistics in Pharmaceutical Quality Control

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

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$449.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

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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