Listings for Pharma Webinars (162)

PRISYM-Logo-cmyk_2013
PRISYM-Logo-cmyk_2013

Label End to End Tracking. Do you have it? Labeling is an integral component within the medical device production process, with manufacturers needing to ensu...

JanWarner
JanWarner

$249.00

Description : This webinar will explain the basic principles of Deviations and Investigations in the pharmaceutical and medical device industries. Particular ...

SusanneManz
SusanneManz

$249.00

Description : "Internal Audit is a required part of an effective quality system. More importantly, it is an incredibly powerful tool to identify areas of non-...

RonSnee
RonSnee

$249.00

Description : The FDA’s Process Validation Guidance calls for “Continued Process Verification” in Stage 3 of the Guidance which focuses on continual assessmen...

JoseMora
JoseMora

$249.00

Description : Do you find yourself constantly struggling to create, manage, and maintain all of the information found in Corrective and Preventive Actions (CA...

AngelaDunston
AngelaDunston

$249.00

Description : This live training webinar will discuss the just issued (July 2015) DRAFT Guidance for Industry on “Request for Quality Metrics” along with how ...

ChrisHayes
ChrisHayes

$249.00

Description : What is a Kata? A Kata is something most often associated with martial arts. It is a routine you practice purposefully with intent of making tha...

John E.Lincon
John E.Lincon

$249.00

Description : The U.S. FDA has stated that the use of a medical device or pharmaceutical entails some degree of risk. In fact, any medical procedure / interve...

CarolynTroiano
CarolynTroiano

$249.00

Description : We will discuss in detail how computer system validation can be applied to mobile applications subject to FDA regulations. This is critical in o...

KenChristie
KenChristie

$249.00

Description : Understand the importance of an effective environmental monitoring (EM) program and its place in your organization. This course will provide ins...

MeenaChettiar
MeenaChettiar

$249.00

Description : Large and small medical device and pharmaceutical companies have a challenge in dealing with their CAPA program, specifically in performing a ti...

Kierstan
Kierstan

$249.00

Description : Cleanliness is a hot topic in the medical device industry. The FDA expects medical device companies to validate the cleanliness of their devices...

ChuckPaul
ChuckPaul

$249.00

Description : This workshop will describe the environment in which success can be fostered with the tools that you already have at your fingertips – complianc...

RobBraido
RobBraido

$249.00

Description : Every medical device company (OEM) must meet certain standards for validation of its transfer plans, facilities, clean rooms and processes. Thes...

DavidLim
DavidLim

$249.00

Description : This seminar is intended to help you adequately implement good social medical practices to avoid FDA enforcement actions for potential misbrandi...

LanceColeman
LanceColeman

$249.00

Description : The awareness and use of data is a direct reflection of the maturity of a company’s management system. Quality Tools are the lens, collectors an...

ChrisDevine
ChrisDevine

$249.00

Description : All industry professionals, regardless of functional roles, will benefit from this training, especially if you are involved in the day-to-day ac...

SusanneManz
SusanneManz

$249.00

Description : Predictive Compliance will help you identify, investigate, and communicate compliance issues within your organization. This webinar will help yo...

AngelaDunston
AngelaDunston

$249.00

Description : The guidance has been developed to address the lack of clarity with respect to what chemistry, manufacturing, and controls (CMC) information in ...

$249.00

Description : The Generic Drug User Fee Amendments of 2012 (GDUFA) were designed to speed the delivery of safe and effective generic drugs to the public and r...

John E.Lincon
John E.Lincon

$249.00

Description : This webinar will discuss about the “Strategic Priorities” that the FDA has published to emphasize their future directions vis-à-vis regulated i...

JoseMora
JoseMora

$249.00

Description : Design controls involve the translation of user requirements (aka Voice of the Customer) into specific technical requirements as design inputs. ...

BrianGalli
BrianGalli

$189.00

Description : Learn how US healthcare reform will impact quality and compliance for healthcare companies such as health insurance, healthcare providers, pharm...

DavidLim
DavidLim

$249.00

Description : Device firms, who are intending to bring medical device products into the US market, are subject to quality system regulations. Recent FDA enfo...

$249.00

Description : This course not only looks at root cause analysis through the lens of identifying deficiencies that need elimination but also from the standpoin...

John E.Lincon
John E.Lincon

$249.00

Description : This training on combination product regulations will evaluate the chief areas of concern or change in the new cGMP requirements for combination...

suefitzpatrick
suefitzpatrick

$249.00

Description : One of the reasons for good clinical practice (GCP) is to protect the subjects in a research trial. In all research the subjects’ well-being sho...

SusanneManz
SusanneManz

$249.00

Description : Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes leading to 483s and ev...

DavidLim
DavidLim

Description : To achieve and remain compliant with the adequate use of the Excel spreadsheet in FDA-regulated environments, it is critical that laboratory per...

$249.00

Description : We will discuss the importance of applying industry best practices when validating systems and applications used in the tobacco industry, as reg...

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