Miguel Montalvo
Instructor Miguel Montalvo
Product Id 600928
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

Outsourcing Management - Effective Contract Manufacturers, Supplier Evaluation, Approval and Monitoring

Overview:

Regulatory agencies hold firms responsible for delivering high quality products that meet all established requirements and specifications. Suppliers and vendors play a key role in accomplishing the GMP mandates and it is the firm's responsibility to make sure vendors/suppliers are meeting specifications for the supplied materials, components, equipment and/or services. For many years, industry has implemented procedures for selection, approval and qualification of suppliers and vendors but, in many cases.

These were not being implemented effectively or formally documented. Making these programs part of a risk-based quality systems approach that the FDA and other regulatory agencies have come to expect from industry is critical. The course will include a process for selection, evaluation, audit, approval and monitoring of vendors/suppliers based on the material/equipment/service being delivered. These decisions must be documented and must be based on the impact (risk) to the final product.

This course will discuss the regulatory expectations and other industrial references/standards that will impact your system. Then, we will discuss the general requirements of a vendor/supplier (outsourcing management) control program followed by specific requirements for different types of supplied materials/equipment/services and the application of a risk-based categorization system. The importance of the audits and the final contract/quality agreement will be included.

Why should you attend: Recently, the FDA is focusing aggressively on these areas based on particular events including the Heparin case from 2008. Another factor is the globalization of our industry when more than 80% of our API's come from outside the US and most of our materials as well. There is a need for an effective plan, risk assessments and adequate resources to deal with outsourcing controls.

Areas Covered in the Session:

  • Regulatory Background and Industry References and Standards
  • Fundamentals of an Outsourcing Management System
    • Procedure and Documentation
    • Pre-requisites - specifications and internal agreements
    • Selection of vendors/suppliers/service providers
    • Audits - a risk-based approach to determine the requirements and levels of the assessments
    • Approval of supplier/vendors - Quality Agreement/Contracts
    • Maintenance of the program
  • Impact of the Quality Agreement/Contract
  • Practical aspects of an Outsourcing Management Systems for Materials and Components
  • Specifics related to equipment/system suppliers
  • Specifics related to Contract Services - Manufacturing, Packaging, Calibrations, Laboratories, Equipment/System Maintenance
  • Monitoring of the Approved Contractors/Suppliers and Management of Change within the Outsourcing Management System

Who Will Benefit:
  • Purchasing
  • Materials Management
  • Development
  • Quality
  • Manufacturing
  • 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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