ENGINEERING PHARMACEUTICAL INNOVATION
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I'm proud to say that I have been an active Member in ISPE for the past 23 years. It has been an incredible journey that has been rewarding personally and influenced my career a great deal. I couldn't imagine being associated with a better group. ISPE has brought me into contact with caring, motivated pharmaceutical professionals who share my passion for making a difference in this industry. The excellent staff and dedicated volunteers that serve ISPE and its Members are a blessing to the Membership and the industry they so ably serve.

Andy Signore, PE, President
IPS, USA

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Training

Basic Concepts of Validation

ISPE CEUs*: 1.3
Type: Classroom Training Course


Date

Location

Country

Instructor(s)

This course is not currently scheduled, but may be conducted on-site. Please contact ISPE Customer Service.

Description

Validation is an integral part in the life cycle of any drug product. This course will provide participants with background and perspective on the purpose and key principles of validation, regulatory aspects, and documentation requirements.

Explore the use of a master validation plan, installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) protocols, and the relationship of validation to the good manufacturing practices (GMPs). Through experiential case studies and exercises, participants will learn how to prepare a validation protocol, analyze data, and prepare a final report.

Take Back to Your Job

  • Discuss the concepts, terminology, and requirements for qualification and validation of pharmaceutical facilities, equipment, and processes
  • Identify the key principles of validation
  • Define the relationship between validation and GMPs
  • Describe FDA inspection expectations for qualification and validation of facilities, equipment, and processes
  • Draft a validation protocol, analyze data, and prepare a final report using an experimental case study and exercise

Attendance Suggested For

  • Validation scientists, quality assurance and control specialists, manufacturing supervisors, technical support personnel, engineers, and all levels of management who want a fundamental understanding of qualification and validation of pharmaceutical facilities, equipment, and processes
  • Professionals from service organizations and vendors who serve pharmaceutical clients

Continuing Education Units

ISPE will provide continuing education units (ISPE CEUs) for all North American seminars and courses, including educational programming at the ISPE Annual Meeting. CEUs are nationally recognized units of achievement designed for those individuals continuing their education in their chosen field or profession.

Delegates attending European seminars and courses will receive a Certificate of Attendance, as ISPE CEUs are currently not offered at European events. Verification of CEUs is based on attendance as well as satisfactory completion of all evaluation materials. Statements of credit will be mailed within four weeks of evaluation materials. One hour of education programming equals 0.1 ISPE CEU credits.

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