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Acceptance activities are common in device manufacturing, but
seem to cause problems for some manufacturers. These problems
range from simple... ...
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compliance training, medical device, adverse event, Data Mining, Drug Safety, risk assessment, Steve Jolley, Warning letters, compliance professionals, statistical methods, Compliance, Compliance Training, SOP, FDA, Regulatory Affairs, Medical Device
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- Categories:Conferences › Healthcare & Medicine ›
5231244
41 views
Language: English

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On July 8, 2010, the FDA announced to soon conduct a series of
inspections related to 21 CFR Part 11. FDA made it very clear that
the focus of the... ...
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FDA warning letters, Computer Validation, computer system validation, Ludwig Huber, FDA compliance, Compliance, FDA, Medical Device, Compliance Training, Design History File, regulatory training, SOP
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- Categories:Conferences › Healthcare & Medicine ›
5231244
79 views
Language: English

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Foodborne illness is often traced to improper cleaning and
sanitizing of food equipment and the environment. Operators of
food facilities develop and ...
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food safety, Standard Operating Procedures, Food Safety training, Sanitation Procedures, Compliance Training, ISO 22000, Food Protection, safety management systems, Training Seminars, FDA, Compliance
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- Categories:Conferences › Healthcare & Medicine ›
5231244
354 views
Language: English

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Laboratories that work in a GMP environment are required to have
documentation to show they are qualified to run specific, consistent
and reliable... ...
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compliance, FDA, ISO, Regulatory Affair, Compliance Training, Webinar, Medical Device
Pharmaceutical products, process development, Quality by Design, GMP environment, Safety Alerts
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- Categories:Conferences › Healthcare & Medicine ›
5231244
39 views
Language: English

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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 ...
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compliance, FDA, ISO, Regulatory Affair, Compliance Training, Webinar, Medical Device
signal detection, data mining, Drug Safety, Drug Information Association, adverse event, statistical signal, World Health Organisation
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- Categories:Conferences › Healthcare & Medicine ›
5231244
45 views
Language: English

pgs. 2
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In this presentation we will explore the requirements for postdesign
risk management and determine how to apply the
requirements. The presentation is ...
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Safety Alerts, Design Verification, risk management, medical device, Risk Management Tools, ISO 14971, Warning Letters, compliance, FDA, ISO, Regulatory Affair, Compliance Training, Webinar, Medical Device
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- Categories:Conferences › Healthcare & Medicine ›
5231244
43 views
Language: English

pgs. 2
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Whether you work in production or in a laboratory or if you conduct
investigations or finalize product release, sound data and
information is... ...
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Documentation Practices, Pharmaceutical Manufacturer, Risk Management Workshops, compliance, FDA, ISO, Regulatory Affair, Compliance Training, Webinar, Medical Device
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- Categories:Conferences › Healthcare & Medicine ›
5231244
168 views
Language: English

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Safety Alerts, drug safety, GMP requirements, Product developers, Pharmaceutical products, HPLC methods, method validation, validation protocol, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
90 views
Language: English

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Live... ...
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Design Verification, Safety Alerts, risk management, medical device, FDA Warning Letters, ISO 14971, Warning Letters, Design Validation, Risk Management Tools, regulatory affairs, active ingredient, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
30 views
Language: English

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Live... ...
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Safety Alerts, Medical Device, cGMP compliance, FDA Warning Letters, John E Lincoln, FDA responses, regulatory affairs, medical industry, supply chain, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
140 views
Language: English

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Live... ...
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Safety Alerts, Global Compliance, HACCP program, Regulatory Compliance Consulting, Food Recall, Food Safety, Quality Assurance, Control Requirements, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
12 views
Language: Italian

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ISO 13485, concepts of accuracy and precision, Risk Management, FDA requirements, FDA QSR, Safety Alerts, FDA Compliance, ISO 14971, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
31 views
Language: English

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Live... ...
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Design Verification, risk management, FDA Warning Letters, ISO 14971, Design Validation, regulatory affairs, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
121 views
Language: English

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Safety Alerts, product recalls, risk management, active ingredient, Design Verification, Compliance Catalog, Regulatory Compliance Consulting, Global Compliance, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
67 views
Language: English

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drug safety, Safety Alerts, GMP requirements, Pharmacovigilance, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
103 views
Language: English

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Safety Alerts, risk management, active ingredient, Design Verification, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
14 views
Language: English

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Safety Alerts, Medical Device, cGMP compliance, FDA Warning Letters, John E Lincoln, regulatory affairs, medical industry, Compliance training, FDA, Compliance, CAPA, Regulations, Medical device, Regulatory Affairs, Quality Eng
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- Categories:Conferences › Healthcare & Medicine ›
5231244
11 views
Language: English
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