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Overview:

Analytical and other equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability. Recent EU and FDA inspection documents prove that qualification, validation and electronic laboratory records are on target of inspectors. The large numbers of FDA warning letters also demonstrate that the industry struggles with either understanding or implementing the regulations.

This 2-day interactive course provides the regulatory background and guides attendees through the complete equipment qualification and computer system validation processes from planning to reporting. It also helps to fully understand not only the text but also the meaning of Part 11 and Annex 11 requirements to ensure and document integrity and other requirements for electronic records and signatures.

The 2-day course not only ensures a full understanding of the regulations and guidelines for equipment and records but also provides templates and examples to develop inspection ready documentation. Interactive exercises will be dispersed into and between the presentations. About 50% of the total time will be dedicated to practical sessions. Here attendees work in small groups on case studies and prepare the answers using prepared fill-in templates. After the course a large variety of tools such as SOPs, validation examples and checklists will be readily available on a dedicated website that can be used by attendees to easily implement what they have learned in the course.

Course Objectives:

  • Learn about the FDA requirements for equipment qualification according to Annex 15, USP <1058>, and computer system validation according to GAMP Guides
  • Learn which equipment/systems need to be qualified or validated
  • Be able to allocate equipment and systems to USP <1058> and GAMP categories and to design and execute qualification/validation protocols accordingly
  • Understand each step and practices of instrument qualification and computer system validation
  • Understand how to archive raw data from hybrid systems: electronic vs. paper
  • Be able to define and demonstrate Part 11 compliance functionality to auditors and inspectors
  • Learn how to ensure and document integrity of raw data and other records according to Part 11 and Annex 11
  • Understand FDA's New and ongoing Part 11 inspection and enforcement practices
  • Be able to develop inspection ready documentation during on-going routine operation
  • Learn how to avoid and/or respond to FDA inspectional observations and warning letters

Who Should Attend?

  • IT/IS managers and system administrators
  • QA managers and personnel
  • Laboratory Managers and Supervisors
  • Analysts
  • Validation Specialists
  • Software Developers
  • Regulatory Affairs
  • Consultants
  • Documentation Departments
  • Training departments

From

  • Pharmaceutical development and Quality control laboratories
  • Quality control laboratories of API manufacturers
  • Contract laboratories
  • Contract manufacturers
  • Clinical Research Organisation
  • Suppliers and service providers of instruments and computer systems

Agenda:

Day 1 Schedule

Lecture 1: Requirements and approaches for Instrument Qualification and Computer System Validation

  • FDA/EU, ICH and PIC/S requirements
  • Lessons from recent FDA Warning Letters and how to avoid them
  • Understanding the terminology: qualification, calibration, verification, validation.
  • EU/PUCS GMP Annex 15: Validation and Qualification
  • USP Chapter <1058> for analytical instruments: current and proposed changes
  • Lessons from GAMP®5 and from the GAMP® guide: "A Risk based Approach to Laboratory Systems"
  • Planning for cost-effective qualification and validation
  • Which instruments require qualification/validation

Lecture 2: Introduction to FDA 21 CFR Part 11 and EU/PICS Annex 11

  • Objective, scope, current situation and future of Part11
  • Requirements overview and spirit of the regulation
  • Requirements for electronic records
  • Requirements for electronic and digital signature
  • Additional requirements from the PICS/EU Annex 11, from the UK MHRA and from the WHO GMP data integrity guidelines
  • FDA/EU inspection and enforcement practices of electronic records: examples of recent FDA warning letters
  • User requirements for Part11/Annex 11 based on risk
  • Upgrading old or purchasing new systems: compliance and business aspects
  • Six steps for implementation of Part11/Annex 11

Lecture 3: Going through the equipment qualification phases

  • Develop a project plan from the master plan
  • Writing requirement specifications
  • Documenting installation and installation qualification
  • Testing for initial operational qualification
  • Preparing and executing test protocols
  • Maintenance, requalification and change control

Lecture 4: Cost Effective Validation of Computer Systems: Step-by-Step - Part 1

  • Selecting the right validation lifecycle model
  • Going through examples of a complete computer system validation from beginning to end
  • How risk assessments can help to determine the type an extent of validation
  • Defining user requirements based on risk
  • Vendor assessment and supplier agreements
  • Going through examples for OQ and PQ testing
  • Writing the validation report

Day 2 Schedule

Lecture 1: Validation of Computer Systems - Part II

  • Leveraging validation efforts of identical systems
  • Validation of existing equipment and computer systems
  • Preparing inspection ready validation documentation
  • Integrating the GAMP® guide with USP <1058> for integrated instrument and system validation
  • IT infrastructure qualification and validation of networked systems
  • Validation and use of cloud computing in FDA/EU regulated environments
  • Recommendations for different cloud models and services

Lecture 2: Validation and control of Excel spreadsheet applications

  • Designing spreadsheets for compliance
  • Validation approach for spreadsheet applications
  • When, what and how much to test?
  • Recommendations from GAMP®5 for testing native Excel functions
  • How to ensure spreadsheet and data integrity
  • Going through examples
  • Excel spreadsheet validation from beginning to the end: A case study that can be used by everybody

Lecture 3: Maintaining the validated state of computer systems or Control of Operation and Retirement

  • Ongoing training of users and IT staff
  • System maintenance and data backup
  • Change control: Handling planned and unplanned changes
  • How to deal with security patches
  • Periodic review vs. revalidation
  • Disaster recovery and business continuity planning
  • Retirement of computer systems and data migration

Lecture 4: Ensuring and documenting Integrity of Laboratory (Raw)data and other Records

  • Learnings from the new FDA guide: Data Integrity and GMP Compliance
  • Definition of raw data and meta data: FDA/EMA requirements
  • What to archive for hybrid systems: paper records or electronic records
  • The importance of electronic audit trail to document data integrity
  • Review of electronic audit trail: who, what, and how
  • How to ensure availability of electronic records throughout the entire retention period
  • Steps for validating security and integrity functions
  • Examples how to ensure and document data integrity and security
  • Preparing your company for data integrity audits

Speaker:

Dr. Ludwig Huber

Chief Advisor - Global FDA compliance, Labcompliance 

  • Chairman, presenter and panel discussion member at US-FDA Industry Training sessions and conferences
  • Served as team member of PDA's task forces "21 CFR Part 11", of US-FDA internal documents, and of the GAMP® special interest group on Laboratory Systems.
  • Presenter of the Year of the Institute for Validation and Technology
  • Director and chief editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories.
  • Author of the books "Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems"

Location: Zurich, Switzerland Date: December 1st and 2nd, 2016 and Time: 9:00 AM to 6:00 PM

Venue: Hilton Zurich Airport

Address: Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland. +41 44 828 50 50

Price: Register now and save $200. (Early Bird)

(Without Stay) Price: $1,695.00 (Seminar for One Delegate)

Until October 15, Early Bird Price: $1,695.00 from October 16 to November 29, Regular Price: $1,895.00

(With Stay) Includes Price: $2,095.00 (Seminar for One Delegate)

Until October 15, Early Bird Price: $2,095.00 from October 16 to November 29, Regular Price: $2,295.00

Register for 5 attendees (With stay)   Includes   Price: $5,343.00 $10,475.00 You Save: $5,132.00 (49%)*

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com               

Website: http://www.globalcompliancepanel.com

Registration Link - http://bit.ly/2dvpeSy-Validation-and-Part11

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel

Not sure if you want to exhibit at or attend the Conference on Validation and Part 11 Compliance of Computer Systems and Data - GlobalCompliancePanel 2016? See the panels below to get the information you need to make an informed decision.

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Website: http://www.globalcompliancepanel.com/...
Conference/Event Dates: 12/01/2016 - 12/02/2016
Conference/Event Hours: 9:00 AM to 6:00 PM
Classification: B2B
Primary Industry: Clinical Pharmacology
Other Industries: Clinical Pharmacology, IT, Professional Healthcare, Technology
Audience: IT/IS managers and system administrators
QA managers and personnel
Laboratory Managers and Supervisors
Analysts
Validation Specialists
Software Developers
Regulatory Affairs
Consultants
Documentation Departments
Training departments
Venue: Hilton Zurich Airport
Venue Type: Indoor - Hotel

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Dr. Ludwig Huber

Chief Advisor - Global FDA compliance, Labcompliance 

  • Chairman, presenter and panel discussion member at US-FDA Industry Training sessions and conferences
  • Served as team member of PDA's task forces "21 CFR Part 11", of US-FDA internal documents, and of the GAMP® special interest group on Laboratory Systems.
  • Presenter of the Year of the Institute for Validation and Technology
  • Director and chief editor of www.labcompliance.com, the global on-line resource for validation and compliance issues for laboratories.
  • Author of the books "Validation and Qualification in Analytical Laboratories, and "Validation of Computerized Analytical and Networked Systems"
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