Upcoming Changes to ISO 14-644 Parts 1 and 2 - Cleanrooms and Associated Controlled Environments
Instructor:
Joseph Winslow
Product ID: 704339
- Duration: 60 Min
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
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.
More Training By Experts
Refund Policy
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
