Attend this session to know about general requirements and best practices to maintain a good documentation.
Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link -
https://www.onlinecompliancepanel.com/webinar/Technical-Writing-Best-Practices-503407/APRIL-2019-ES-TRAININGREGISTRY
It is quite common between departments or individuals to neglect seeing the importance of 21 CFR Part 11 and Annex 11 (ERES) Compliance. Non-QA trained personnel or those that have no direct or have indirect contact with GxP systems fail to see the consequences of their actions or that of their department.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/21CFR-PART-11-ANNEX-11-COMPLIANCE-501871/NOVEMBER-2016-ES-TRAININGREGISTRY
Don't be caught unaware of the changes in income tax due to IRS notices, announcements, and annual Rulings. Some tax laws have not changed in 2016, some were made permanent and some have changed. There is enough time between now and December 31 for persons to make investments, contributions, etc. which can lower their 2016 individual income tax bill to the IRS. Fail to plan and plan to fail.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/FEDERAL-TAX-UPDATE-501763/OCTOBER-2016-ES-TRAININGREGISTRY
Regulations mandate effective content control. In an era of continuous flow of information and a regulatory guidance for Knowledge Management (KM) as an enabler of Pharmaceutical Quality System (PQS) Pharmaceutical and Biopharmaceutical firms realize the need to have easy to use Document Control and Management Solutions (DCMS).Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/DOCUMENT-CONTROL-SYSTEMS-501811/OCTOBER-2016-ES-TRAININGREGISTRY
This webinar will focus on effective communication of technical information so that an external auditor will quickly understand it and credit your organization with doing the job right.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/TECHNICAL-WRITING-MEDICAL-PRODUCTS-501724/SEPTEMBER-2016-ES-TRAININGREGISTRY
This course is designed to provide participants with tools for writing effective Standard Operating Procedures. A general process for creating and implementing SOPs will be presented, including discussion on the important sections which should be included in each SOP, how to generate the consensus ultimately required for the SOPs to be followed consistently, training requirements and post-implementation evaluation and periodic review. We will discuss a list of SOPs which every analytical laboratory should have.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/WRITING-EFFECTIVE-SPOs-GMP-LABORATORY-501541/JULY-2016-ES-TRAININGREGISTRY
This Webinar will cover how to conduct a human factors analysis of instructional documents, which is a critical task to perform for existing documents. The concepts from this session can be incorporated into the creation of new instructional documents also.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/HUMAN-FACTOR-ANALYSIS-PARTICULARLY-MBR-SOP-501574/JULY-2016-ES-TRAININGREGISTRY
This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train attendees on effectively reviewing and revising documents and assessing your audience, in effect producing effective written correspondence.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/TECHNICAL-WRITING-PHARMACEUTICAL-MEDICAL-BIOTECH-501535/JUNE-2016-ES-TRAININGREGISTRY
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