ComplianceOnline

Cleanroom Design, Certification & Classification

Instructor: Nazia Dar
Product ID: 700404
Training Level: Basic
  • Duration: 60 Min

recorded version

$249.00
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
Last Recorded Date: May-2007

Training CD

$500.00
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: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This Pharmaceutical training will also provide attendees with the details and expectation stipulated in ISO 14644 series standards and FDA’s 2004 guidance document for aseptic processing.

Description

This seminar is designed to provide a thorough understanding of the principles applied to the design, qualification and operation of cleanrooms.

The testing procedures and the regulatory requirements with regard to cleanrooms qualification and certification will be discussed. This course will also provide attendees with the details and expectation stipulated in ISO 14644 series standards and FDA’s 2004 guidance document for aseptic processing.

Areas Covered in the seminar:

  • Design, qualification and operation of cleanrooms
  • The testing procedures
  • ISO 14644 series standards
  • FDA’s 2004 guidance document for aseptic processing

Who Will Benefit:

Personnel working in sterile pharmaceutical manufacturing facilities and are responsible and involved in the activities, such as the cleanrooms qualification, maintenance, operation and monitoring at an ongoing basis.

  • Validation staff
  • Engineering Staff
  • Microbiologist
  • Production management and staff directly involved in cleanroom operation
  • QA staff
  • Team members of Quality Management System (QMS)
  • Contractors
  • Consultants

Instructor Profile:

Nazia Dar, has over 25 years of experience in sterile and non sterile Pharmaceuticals and Cosmetic industries. She holds B.Sc. degree in Microbiology and Biochemistry and received ISO 9001:2000 Auditor Certificate from AQS. She has a proven records of continuous improvement based on data trending and investigations. Her past technical experience includes several management positions in the areas of Production, QC, QA, Validation, and Process Development at multinational pharmaceutical organizations. Nazia is a presenter of several courses and seminars to pharmaceutical professionals in Canada and overseas. Her areas of expertise are the Microbiological Environments, Cleanroom Controls and Sterilization Processes. Nazia is active member of PSG and DIA and is a member of IEST & PDA.

Follow us :
Validation, Verification and Transfer of Analytical Methods
Upcoming In-person Seminars by EX-FDA OFFICIALS

Refund Policy

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.

If you have any concern about the content of the webinar and not satisfied 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 customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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