Industry Specific Training Courses

Overview: This training program will cover statistical hypothesis testing concepts including: null and alternate hypotheses, test statistics, p-values, confidence intervals, confidence levels, power, power curves, and sample sizes. Several types of hypothesis tests will be covered such as 1 and 2-sample means tests, tests of variances, and tests of proportions. Equivalence tests will also be discussed. The importance of selecting appropriate sample sizes will be stressed.

Overview: This webinar will help you develop a quality control program that fits your microbiological laboratory's needs. We will explicitly not cover any serological, immunological or molecular tests. Why should you Attend: In microbiology laboratories, there are a wide array and media for all sorts of use. From clinical laboratories, to environmental monitoring, from research laboratories to industrial labs, there are a large number of different set-ups. These media and reagents need to be monitored on a regular basis to ensure that the work performed in these laboratories is accurate and true. Otherwise, false results will be reported, which can lead to serious consequences and harm the public health in a myriad of ways.

Why should you Attend: Per ICH Q10 Quality risk management is integral to an effective pharmaceutical quality system It can provide a proactive approach to identifying, scientifically evaluating and Controlling potential risks to quality Integrating the principles of QRM into our quality processes is complex especially in a pharmaceutical organization There is much confusion on how to define risk and individuals often think of quality risk management as just a tool like FMEA analysis verses an overall QRM approach This training will explain the important concepts associated with a QRM approach

This webinar discusses the current technology transfer procedures which are practiced by pharmaceutical and biopharmaceutical firms. 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/Best-Practices-for-Effective-Pharma-Technology-Transfer-From-R-D-to-Clinical-to-Commercial-507045/APRIL-2019-ES-TRAININGREGISTRY

Learn about elemental impurities either through thorough risk assessments or through testing. And it will provide an understanding of the standards and guidelines. 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/Elemental-Impurities-Tests-for-Pharmaceutical-Products-according-to-the-ICH-Q3D-and-USP-232-233-Guidelines-507031/APRIL-2019-ES-TRAININGREGISTRY

Join the webinar to learn legal liabilities for check frauds and to mitigate risks which could be expensive. 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/Legal-Liabilities-when-Check-Fraud-Occurs-504219/APRIL-2019-ES-TRAININGREGISTRY

Attend this webinar to learn the most important areas of medical device safety and how complaint handling and CAPA process is used during FDA inspections. 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/Medical-Device-Complaints-CAPA-506097/APRIL-2019-ES-TRAININGREGISTRY

Learn how to use controls and segregation of duties to build a bullet-proof AP operation without compromising efficiency of AP operations. One hour Webinar. 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/Using-Controls-and-Segregation-of-Duties-to-Build-a-Bullet-Proof-AP-Operation-504288/APRIL-2019-ES-TRAININGREGISTRY

Learn all the new SFCR rules which focus on food safety needs along with avoiding penalties by complying with the regulations. 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/New-Safe-Foods-for-Canadians-Regulation-508013/APRIL-2019-ES-TRAININGREGISTRY

A discussion on the history and origin of a model validation and understand the requirements by the OCC for a model validation. Join today. 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/AML-Model-Validation-A-Critical-Need-in-the-New-Regulatory-Environment-502661/APRIL-2019-ES-TRAININGREGISTRY

Substandard product can exist even if the product itself is manufactured according to quality standards. Muhammad H. Zaman, in his book Bitter Pills, recalls his visit to a warehouse in Ghana that had no climate control, with temperatures in the warehouse reaching 95 degrees Fahrenheit. Recently, Allergan's Taytulla birth control products were recalled due to the packaging of active tablets and inert tablets in the wrong order, potentially leading to patients likewise taking the tablets in the wrong order and not obtaining the desired result. Allergan stated, "As a result of this packaging error, oral contraceptive capsules that are taken out of sequence may place the user at risk for contraceptive failure and unintended pregnancy."

Overview During this webinar, we will discuss a practical QC approach for in-house prepared and/or commercially purchased media, test kits and reagents specifically applicable to microbiology laboratories to assess the acceptability of the performance of analytical materials, to meet not only their requirements, but also to meet the requirements of ISO/IEC 17025. Why should you Attend Many laboratories are unsure about which QC practices are needed and what criteria to use to assess the acceptability of the performance of analytical materials, to meet not only their requirements, but also to meet the requirements of ISO/IEC 17025.

Any firm reprocessing another manufacturer's medical device becomes the legal manufacturer with all the responsibilities for compliance, especially sterility. Failure to prove sterility is almost certainly a cause for either voluntary recall or FDA mandated recall. The same is true if you are reprocessing your own medical device. If intended to be re-sterilized by the user facility, cleaning and sterilization instructions must be precise and validated. Much attention has been paid to the regulatory requirements of reprocessing single use devices.

The purpose of this training is to provide you with an overview of the Technology Transfer. Define technology transfer. Identify New Product transfer process. Identify elements of the business process framework for managing technology transfers. Explain benefits of technology transfer. Determine elements of a successful technology transfer.

Attend this webinar to learn the new accounting standards to recognize the lease characteristics in transactions. 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/Implementing-the-New-Lease-Accounting-Standards-503332/MARCH-2019-ES-TRAININGREGISTRY

Learn how to prepare for FDA inspection techniques on laboratory controls. 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/Laboratory-Controls-Anticipate-the-Systems-Based-FDA-Inspection-503311/MARCH-2019-ES-TRAININGREGISTRY

This course will discuss the process of developing safety controls by implementing behavior based safety analysis. 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/OSHA-s-Lean-Behavior-Based-Safety-507163/MARCH-2019-ES-TRAININGREGISTRY

This webinar will provide valuable guidance on how to use extraction techniques to validate the cleanliness of a device. 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/Cleaning-Validations-Using-Extraction-Techniques-504912/MARCH-2019-ES-TRAININGREGISTRY

Learn how to create and maintain good documentation that meets FDA computer system validation and compliance standard. Register for this webinar today. 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/Good-Documentation-Practices-to-Support-FDA-Computer-System-Validation-and-Compliance-502210/MARCH-2019-ES-TRAININGREGISTRY

This session will explain the calculation of loan amount needed to support financial projection and borrower's repayment ability. 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/Cash-Flow-Projections-for-Assessing-Borrower-s-Ability-to-Repay-508409/MARCH-2019-ES-TRAININGREGISTRY