netzealous.com
NetZealous
http://www.netzealous.com/services.html
Being a comprehensive training source, NetZealous offers a number of highly flexible web seminars (webinars) that are current, up-to-date and relevant to industry trends. These webinar courses are appropriately structured and are cost-effective. NetZealous' webinars offer the following advantages to the participant:. Equips the participant with the latest happenings in the area of compliance and regulatory aspects online;. Our webinars destroy the barrier of distance between the tutor and the student;.
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FDA 21 CFR Part 11 Compliance | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2015/06/04/fda-21-cfr-part-11-compliance
Your Gateway to Regulatory Compliance. FDA 21 CFR Part 11 Compliance. FDA 21 CFR Part 11 Compliance. June 4, 2015. FDA 21 CFR Part 11 Compliance. FDA 21 CFR Part 11 Compliance sets out benchmarks by which FDA-regulated industries’ electronic signatures and other records are considered authentic. From 2007, a strong body of opinion has emerged challenging the stringency of these requirements, but nothing major has been diluted from these. Which industries are included in FDA 21 CFR Part 11 Compliance?
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February | 2013 | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2013/02
Your Gateway to Regulatory Compliance. GolbalCompliancePanel will Conduct webinar on “Root Cause Analysis”. February 13, 2013. This course provides clarification of the competencies to plan effective, efficient and thorough investigations and design a process for the successful elimination of recurring failures and deviations. Why you should attend. Areas Covered in the Session:. Phases of an investigation. Definition and Principles of Root Cause analysis. Skills of an Investigator.
globalcompliancepaneltraining.wordpress.com
May | 2013 | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2013/05
Your Gateway to Regulatory Compliance. May 3, 2013. USP method transfer underwent a change when the US Pharmacopoeia published the final version of its informational chapter 1224, which deals with the transfer of analytical procedures mentioned in the document entitled USP 35-NF 30. This became official in May 2012. How is the new document different? What are the major elements of the new USP method transfer version? The written analytical procedure and development validation reports have to be transferr...
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GMP Compliance for Pharmaceutical Laboratories | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2015/06/09/gmp-compliance-for-pharmaceutical-laboratories
Your Gateway to Regulatory Compliance. GMP Compliance for Pharmaceutical Laboratories. GMP Compliance for Pharmaceutical Laboratories. June 9, 2015. GMP Compliance for Pharmaceutical Laboratories. In order to ensure GMP compliance, pharmaceutical laboratories have to devise a holistic and long term plan that covers all aspects of the laboratory’s activities. Products must meet high quality standards consistently. They should fulfil their intended use. GMP regulations of EU and the US. The next important ...
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Going by the FDA 21 CFR Part 11 Checklist is a good way to stay on track | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2015/06/04/going-by-the-fda-21-cfr-part-11-checklist-is-a-good-way-to-stay-on-track
Your Gateway to Regulatory Compliance. Going by the FDA 21 CFR Part 11 Checklist is a good way to stay on track. Going by the FDA 21 CFR Part 11 Checklist is a good way to stay on track. June 4, 2015. June 4, 2015. Going by the FDA 21 CFR Part 11 Checklist is a good way to stay on track. It makes sense for organizations that are part of 21 CFR Part 11 to have a checklist of requirements, as this helps eliminate thorny issues. The benefits of charting out an FDA 21 CFR Part 11 checklist are many:. Enter y...
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Batch manufacturing record in pharmaceutical industry | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2013/06/13/batch-manufacturing-record-in-pharmaceutical-industry/comment-page-1
Your Gateway to Regulatory Compliance. Batch manufacturing record in pharmaceutical industry. Batch manufacturing record in pharmaceutical industry. June 13, 2013. In the light of this definition, batch manufacturing record in pharmaceutical industry has to be understood as one that is basically based on the master formula record. It is created, checked, ratified and sanctioned by the designated, competent technical person/s that is responsible for the organization’s production and quality control. Whene...
globalcompliancepaneltraining.wordpress.com
June | 2013 | globalcompliancepaneltraining
https://globalcompliancepaneltraining.wordpress.com/2013/06
Your Gateway to Regulatory Compliance. Understanding the calibration curve. June 13, 2013. How to go about a calibration curve? In understanding the calibration curve, we have to know that a number of stages go into calibrating an analytical instrument. This is how a logical sequence of steps would look:. Planning of the experiments;. Making the relevant measurements;. Plotting the results;. Carrying out regression analysis on the data, which will help obtain the calibration function;. June 13, 2013.
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