ComplianceOnline

Creating Effective SOPs for Regulatory Compliance

Instructor: Henry Urbach
Product ID: 702999
Training Level: Intermediate to Advanced
  • Duration: 60 Min

recorded version

$279.00
1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section

Training CD

$349.00
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 FDA documentation webinar will explain the regulatory expectations for, and the proper design and maintenance of effective and compliant standard operating procedures (SOPs).

Why Should You Attend:

The lack of or inadequate standard operating procedures (SOPs) continue to dominate the FDA's inspectional observations. Their frequency lags only behind the quality unit concerns. Moreover, SOPs are often used as training tools, which means that they need to be easily understood by all those whom they affect. Effective SOPs are not only a regulatory requirement; they also make good business sense. Too many times employees fail to follow SOPs because they can't understand them, and too many times procedures are being constantly revised. This leads to lengthy and expensive investigations and costly revisions.

By attending this webinar, you will gain a better understanding of the regulatory expectations for, and the proper design and maintenance of effective and compliant standard operating procedures. You will also learn how to create and review SOPs, and generate a system for training and implementation of effective and compliant written procedures.

Areas Covered in the Webinar:

  • Why do we have written procedures?
  • What does FDA expect from our written documentation?
  • Regulatory requirements for the creation, compliance and maintenance of written procedures.
  • Proven techniques for creating effective SOPs and other written documents to minimize costly revisions.
  • An effective review and approval process compliant with regulatory requirements.
  • A system for training and implementation of written procedures.
  • A system for the control, archival, and disposal of written procedures.

Who Will Benefit:

  • QA/ QC
  • Regulatory affairs
  • IT/ IS
  • Technical writers
  • General staff with the responsibility for creating, reviewing and approving written standard operating procedures and instructions

Instructor Profile:

Henry Urbach, is the founder of GMP Training, Development and Consulting, GMP TDC LLC, a New York-based consulting organization serving Life Sciences industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in GMP Training and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of a post-regulatory action remediation, and developing an environmental monitoring training program for major pharmaceutical and biotechnology organizations. He is a dynamic speaker specializing in FDA and ICH compliance. He is a Certified Quality Auditor. His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP TEA, a national organization of Life Sciences training professionals.

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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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