Seminar on Equipment, Facility, & Process Qualification and Validation

This event qualifies for 12 CEUs

Course "Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

Companies face many common issues and confusion when creating or revamping their validation programs. Some of these common issues are:

Company has expertise in its process validation program but can never quite get is arms around the facility and equipment changes that require never ending equipment qualification (IQ, OQ, PQ),
Customer or 483 audit findings require the company to deviate from its own validation program to meet the needs of the FDA or the customer
For systems that employ software and hardware, how does the company manage the validation activities (i.e. through the software validation effort or through the equipment qualification program?

Well, the answers to these and many, many more typical questions are now available in this simple to understand, yet detailed training session designed to help manufacturers of FDA regulated products build (or rebuild) a sustainable validation program.

Why should you attend?

Attend this FDA validation seminar to get deep knowledge about:

How to define a Sustainable Structure of a Firm's Validation Program
Understand How Change Control and Other Quality Programs Feed Into the Validation Program
Offer Usable Protocol and Other Validation Program Document Templates
Define Minimal Recommended Tests and Verifications for
Equipment Qualification
Process Validation
Software Validation

Common Pitfalls to Avoid When Executing Validation Protocols How to Estimate Costs and Time Associated with Validation How to Respond to Customer and Regulatory Audit Observations Associated with Validation

Areas Covered in the Session:

Basics Of Validation
The Components of a Sustainable Validation Program
Other Programs that Feed the Validation Program (1 Hour)
Equipment, Utility, and Facility Qualification
Process Validation
Software Validation
Time and Costs of Validation
Responding to Validation and Other Related Audit Findings

Who will benefit:

Internal Auditors
Regulators
Legal Departments
Compliance Officers
Validation Managers
QC Managers
QA Managers
Facilities and Engineering Department Staff

Agenda:

Day 1 Schedule:

Lecture 1: Understanding the Basics of Validation

Regulatory References
Validation Terminology

Lecture 2: The Components of a Sustainable Validation Program

Design Qualification
FATs and SATs
Commissioning
The Validation Master Plan
The Validation Project Plan
Standard Operating Procedures (SOPs)
Protocols
Reports
Additional Software Validation Documents

Lecture 3: Other Programs that Feed the Validation Program

Change Control
Complaint Handling
CAPAs
Deviation Management
Maintenance
Sales

Lecture 4: Equipment, Utility, and Facility Qualification

The SOP
Protocol Template
Minimal Testing and Verifications for IOQ
Minimal Testing and Verifications for PQ
Facility Qualification
Execution of Protocols
Report Generation

Lecture 5: Process Validation

The SOP
Protocol Template
Minimal Testing and Verifications
Execution of Protocols
Report Generation

Lecture 6: Software Validation

The SOP
Protocol Template
Additional Software Validation Document Templates
Minimal Testing and Verifications
Execution of Protocols
Report Generation

Lecture 7: Time and Costs Associated with Validation

Estimating Time Associated with Each "Deliverable"
Hidden Costs of Validation
Estimating Costs of Using Validation Consultants
How to Recoup Costs Associated with Validation for Contract Manufacturers

Lecture 8: Responding to Audit Findings Associated with Validation

Day 2 Schedule:

Lecture 9:Welcome and Day 1 Reinforcement

Lecture 10: Practical Application # 1 -Equipment Qualification

Lecture 11:Practical Application # 2 -483 Responses

Lecture 12:Closing Comments

Individual/Open Q&A Session

Location: St. Petersburg, FLDate: December 3rd & 4th, 2015Time: 9 AM to 6 PM

Venue: Courtyard St. Petersburg Downtown

Address: 300 4th St N, St Petersburg, FL 33701, United States

Price: $1,295.00 (Seminar for One Delegate)

Register now and save $200.

Until November 15, Early Bird Price: $1,295.00

From November 16 to December 01, Regular Price: $1,495.00

Registration Details:

NetZealous LLC - DBA GlobalCompliancePanel

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

USA Phone: 1-800-447-9407

Fax: 302-288-6884

support@globalcompliancepanel.com

http://www.globalcompliancepanel.com

Registration Link - http://bit.ly/1PR53NH

Speaker and Presenter Information

Jonathan M. Lewis

Principal, Advanced Biomedical Consulting (ABC), LLC

Jonathan M. Lewis Founding Partner, Reliant FDA Experts��...a Division of Advanced Biomedical Consulting, LLC, has over twenty-three years' experience in the areas of quality control/quality assurance (QA/QC), regulatory affairs, manufacturing, validation, project management, and executive management in both industry and consulting roles. Mr. Lewis has experience in the medical device, diagnostic, biopharmaceutical, pharmaceutical, cosmetic, nutritional supplement, food, and animal food industries.

Prior to founding Reliant FDA Experts��, Mr. Lewis worked for KMI/PAREXEL, a regulatory compliance and validation consulting firm, in increasing roles of responsibility from an entry-level Validation Engineer to an Associate xDirector of Consulting. He has worked at RPScherer (Cardinal Health), a contract and proprietary solid oral dose pharmaceutical manufacturing facility, as the QC/Validation Manager. In addition, he has worked at Telectronics Pacing Systems, a medical device manufacturer, in Sterility Assurance.