Upcoming Changes to ISO 14-644 Parts 1 and 2 - Cleanrooms and Associated Controlled Environments

Instructor: Joseph Winslow
Product ID: 704339
  • Duration: 60 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556


Read Frequently Asked Questions

Attendees will come away from this training program with a good understanding of upcoming changes to the ISO standard and the implication of those changes to the classification and operation of clean rooms in regulated industries.

Why Should You Attend:

ISO-14-644 parts one and two are the standard to which clean rooms in many industries are classified and maintained. The standard has been under consideration for revision for several years by the committee, and now that revision is imminent.

This webinar will go over the proposed revisions, when those revisions will take effect, and what the impact will be to your clean room. If your company operates in a cleanroom environment, and your role is to classify, validate, operate, or maintain those clean rooms, then this webinar can help ensure that your company continues to operate in line with the updated standard.

Areas Covered in the Webinar:

  • Short background on the standard
  • Changes to ISO 14-644 Part 1 and implications to regulated industries
  • Changes to ISO 14-644 Part 2 and implications to regulated industries
  • Effective date of change
  • Q&A

Who Will Benefit:

Personnel in any industry with regulated cleanrooms and who are in the following positions should attend:

  • Facilities
  • Engineering
  • Quality Assurance
  • Quality Control (Micro)
  • Operations
  • Maintenance
  • Calibration
  • Validation
  • Anyone with responsibilities for designing, classifying, qualifying or operating clean rooms that are regulated by the ISO standard

Instructor Profile:

Joseph Winslow has over 20 years of experience as a leader, engineer, and executive in the highly regulated industries of pharmaceuticals and medical devices. His wide range of experience includes facilities, construction, manufacturing, logistics, maintenance, safety, and IT.

He is one of just over 100 professionals worldwide that have been certified by the International Society of Pharmaceutical Engineers as a Certified Pharmaceutical Industry Professional (CPIP). In par with the certification, his technical knowledge extents to product development, facilities and equipment, information systems, supply chain management, production systems, regulatory compliance including drugs and EH&S, and quality systems.

Mr. Winslow currently works as a consultant to FDA regulated industries in his areas of expertise.

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