Miguel Montalvo
Instructor Miguel Montalvo
Product Id 600935
Duration 90 Minutes
Version Recorded
Original Price $295
Special Offer Price $10
Refund Policy
Access recorded version only for one participant; unlimited viewing for 6 months

Effective and Compliant Change Control Management - Before, During and After Validation

Overview:

There is a need to implement an adequate formal level of change control during engineering projects (referred to as an Engineering Change Control) after the approval of the equipment/systems specifications in addition to the more formal change control after the qualification of these systems. The Engineering change control process will apply through design, construction and qualification up to the point that the system is considered installed/operational. The new Quality Systems guideline from the FDA states that the Quality function must be involved in the review of the design and subsequent changes to the design of facilities, equipment and systems that may impact the product quality.

Why should you attend: Most pharmaceutical companies focuses on change control management after commercialization but changes must be managed earlier during the design of facilities, equipment and systems in addition to changes implemented during the development of the manufacturing processes. The question is: What is the level of control required at the design/development stages? Who needs to be involved? What are the steps required for the processing of such changes and the documentation that is required to provide evidence of such controls?

Course Modules & Content Details:

  • Specifications Change Control - Handling of changes to URS, FRS, Design Specifications and When do we implement some level of Change control
  • Design Change Control - Relationship between Design Qualification/Review and Change Control and Adequate/Practical Documentation Requirements for changes during design - handling of drawings
  • Change Control during Construction, Start-Up and Commissioning
  • Formal Change Control Management after Equipment/Systems Qualification
    • Definitions - Like for Like, Emergency/Unplanned vs. Normal/Planned Changes
    • Applications for Documentation Changes
    • Applications for Process Changes
    • Applications for Changes in equipment/systems

Who Will Benefit:
  • Manufacturing
  • R&D
  • Quality
  • Validation
  • Engineering
  • Top Management

Speaker Profile
Miguel Montalvo, B.S. Chem. Eng., MBA, President, Expert Validation Consulting, has over twenty-eight years of professional/management experience in positions of increasing responsibility in the areas of Quality, Validations and Technical Services within the traditional pharmaceutical, OTC Drugs, cosmetics, dietary supplements, biotechnology and medical device industries including extensive expertise on development and implementation of quality functional procedures (QA/QC), Quality Systems, GMP/QSR compliance audits (internal, supplier, external audits), remediation projects with companies on consent decrees, handling of non-conformances (OOS, investigations and deviations), Process/Cleaning/Computer Systems/Equipment/Facility validations, Change Control, CAPA, international GMP compliance, Calibrations, Risk Management, operational compliance assessments/Gap Analysis and start-up of manufacturing facilities.

He is a well-recognized international speaker on GMP Compliance, Validation and Quality related topics for organizations such as IVT, PDA-TRI, CfPIE and Barnett International and his articles/papers have been published in the American Pharmaceutical Review and the Journal of Validation Technology publications and have been published as an author of specific chapters in several design/quality/validation related internationally-recognized reference books. He is a member of the Journal of Validation Technology editorial board and of the PDA Annual Program Committee for their Annual meetings.

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