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From GlobalCompliancePanel
Introduction to Contamination Control Master Plans - By GlobalCompliancePanel
...nation control elements to ensure easy compliance. A CCMP defines to your organization, as well as to auditors, how you mitigate the risks of the specific contaminants for your products.
Areas Covered in the Session:
What is a CCMP and how is it valuable to my company?
What topics are covered in the CCMP and to what extent?
How is the CCMP controlled and updated?
How is the CCMP
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Webinar on Specification Development - By GlobalCompliancePanel
A good specification not only defines the product and process being purchased by the customer, but also serves as an extension of the purchasing contract.
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Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
...g:
* Obtain a brief from the Project Sponsor which defines the clinical trial objectives, rationale, outline timeframe, and estimated budget available
* Review literature and other available information
* Discuss the therapeutic areas with experts in the company and externally such as key opinion leaders, patient groups may also be of help
* Decide on the study design
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Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel
...nation control elements to ensure easy compliance. A CCMP defines to your organization, as well as to auditors, how you mitigate the risks of the specific contaminants for your products.
Areas Covered In the Seminar:
* What is a CCMP and how is it valuable to my company?
* What topics are covered in the CCMP and to what extent?
* How is the CCMP controlled and updated?
more...
Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
...defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product.
Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles and the processes
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Full Day Virtual Seminar - Designing and Implementing the Quality System for Combination Products - by GlobalCompliancePanel
...defines combination products as a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product.
Although there are differences between these quality systems, the quality principles embodied in the systems are the same. This course looks at these principles and the processes
more...
FDAs Update on Medical Device Labeling Changes - Webinar by GlobalCompliancePanel
FDA recently released a final rule regarding the parameters in which a device manufacturer can modify label changes to a product.
Specifically, manufacturers can add or strengthen the contraindications, warnings, precautions or adverse reactions sections of labeling via a PMA supplement without prior FDA approval only when such modifications are based on newly acquired information and evidence
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Signal Detection and Data Mining - Webinar by GlobalCompliancePanel
This webinar will cover the fundamentals of signal detection, and how these can be augmented by the use of data mining techniques.
In March 2005, the FDA published final guidance on "Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment." This guidance defines the FDA's views on pharmacovigilance concepts, safety signal identification, pharmacoepidemiologic assessment and
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Specification Development
GlobalCompliancePanel brings a new webinar on the topic of Specification Development.
Webinar will be on March 23, 2010. Webinar will be presented by Melinda Allen.
A good specification not only defines the product and process being purchased by the customer, but also serves as an extension of the purchasing contract. Specifications are a customers greatest tool for ensuring products received
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From Pioneer Engineering
Condition Based Monitoring CBM Program Selection


...trasonics, and Motor Circuit Signature Analysis. Then it defines the decision points required to make the right choice of which technologies fits your needs and how much/ how often to apply each. It reviews the decision point and program aspect required to choose between staffing a PdM program with in-house resources, outsourced resources, or a hybrid program utilizing both in-house and
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From Business Expert Webinars
Dogs are born to hunt. Is your sales staff born to sell?
...g not to mention lost sales and customers.
This webinar defines the importance of building a sales team with strong DNA. You will learn how different markets need different DNA and be introduced to tools and processes to successfully identify the specific DNA required for your market.
Discussion:
1. Four crucial elements of Sales DNA and their importance to the sales success.
2. Understand
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Develop A Marketing Plan to Retain and Grow Your Customer Base
...nts to measure and analyze
Prepare a research brief that defines the scope of the customer research initiative
Design and use online surveys to gather customer data
Solicit honest customer feedback using comment cards or email
Determine when you need an outside research source and how to select the right one
Analyze the data to develop an effective customer marketing campaign
As an added
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