Listings for Pharma Webinars (166)

$299-399

Aligning Your Company Assets with the BRC Countries’ Medical Needs With strong economic growth, a combined population of nearly 2 billion people, and signi...

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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...

$249.00

Description : How you manage cyber security issues for medical device software raises serious concerns at FDA. Software is subject to a number of FDA requirem...

$249.00

Description : All Regulatory Agencies are entitled to come in to any company involved in clinical trials and review documentation supporting procedures and co...

RonSnee
RonSnee

$249.00

Description : The Pharmaceutical and Biotech industries are going through tremendous changes that have been increased by the recent global financial challenge...

LudwigHuber
LudwigHuber

$249.00

Description : Complying with GLP regulations can increase the cost of a laboratory up to 30%. Companies or employees either don't know exactly what GLP really...

JoseMora
JoseMora

$149.00

Description : Risk management overarches projects associated with a particular product family, given that risks will both remain and change as new design feat...

RobBraido
RobBraido

$249.00

Description : 5 Different Successful Case Studies from Fortune 500 Corporate Innovation Leaders: There is one case study from the oil industry and four case s...

JohnZorich
JohnZorich

$249.00

Description : The seminar begins with an examination of the fundamental vocabulary and concepts related to metrology. Topics include: accuracy, precision, cal...

AngelaDunston
AngelaDunston

$249.00

Description : The pharmaceutical industry is expected to make arrangements to ensure that the accuracy, completeness, content, and meaning of data are retaine...

BrianGalli
BrianGalli

$249.00

Description : Gain an understanding of what an ISO audit is, what an audit entails, and the best practices any organization can use to prepare and successfull...

CarolynTroiano
CarolynTroiano

$249.00

Description : We will discuss the importance of applying industry best practices when managing projects involving development, configuration, implementation, ...

Webinar Instructor - Social Media in Clinical Trials
Webinar Instructor - Social Media in Clinical Trials

$189.00

One of the things that the FDA most commonly finds during audits is bad documentation practices. Companies are frequently cited for missing or incomplete record...

Webinar Instructor - Social Media in Clinical Trials
Webinar Instructor - Social Media in Clinical Trials

$189.00

Social media is a great tool that enables companies to highlight specific issues, addressing concerns, educating patients and doctors alike, and engaging multip...

704122
704122

$199.00

This training program will focus on the importance of procedures. Attendees will learn why people avoid procedures and understand common human errors and deviat...

702282
702282

$249.00

This FDA GMP training will help you understand the current requirements for raw material management with tips for practical implementation. It covers FDA’s expe...

703000
703000

$229.00

This life science product stability testing webinar will explain, in detail, the requirements of the FDA’s drug stability guidelines that are stipulated for dru...

701991
701991

$299.00

This training will cover several recommendations to improve the hospital’s due diligence when administering and dispensing narcotic drugs in a hospital setting ...

704109
704109

$149.00

This training program will elucidate IRB composition, responsibilities and function and detail the types of review processes and regulatory guidelines. It will ...

Compliance Trainings
Compliance Trainings

$249.00

Live Webinar on Thursday, February 14, 2013 Duration: 90 minutes If your design and manufacturing resources are spending too much time on documentation and ...

In this webinar you will learn: * How to stop using paper printouts for particle counting results while maintaining 21 CFR part 11 Compliance * How to mee...

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$1,799.00

Course Description This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and cli...

$1,799.00

Most medical devices marketed in the European Union must follow the Medical Device Directive (MDD); IVD device and active implantable devices have other directi...

Xcelience is delighted to present a free webinar from their "Scentific Seminar Series." These webinars engage the pharmaceutical community about the challenges...

$479.00

An interactive workshop to ensure you understand how to obtain a 510(k) in today's environment at FDA. Knowing how to get your application through FDA quickl...

You are considering implementing a new clinical trial management system (CTMS), or maybe you have already made the decision. But you are wondering: What should ...

As your organization implements or upgrades to a newer version of Oracle Clinical (OC) and Remote Data Capture (RDC), there are many considerations to take into...

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