Listings for Pharma Webinars (173)

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trailblazer_banner_webinar3_300x250-xcon

For nimble biotech companies, the time and effort in getting clinical trials up and running can be frustrating, but many drug developers are turning to new tech...

LinkedIn_CGMP Guidelines In Preparation For FDA Inspection And Trends_ Dos And Donts
LinkedIn_CGMP Guidelines In Preparation For FDA Inspection And Trends_ Dos And Donts

Get discount of $30 on any first webinar In FDA-regulated industry, it is imperative that firms should be well aware of recent policy changes and understand ...

Clinical trial
Clinical trial

The timeliness of bringing new health products and drugs to market for patients is critical. Yet, meeting stringent regulations such as ICH E6 and patient prote...

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trailblazer_banner_xconomy_300x250

Even the very best ideas may struggle to become successful biotech companies without the right partnerships. One of the biggest investments for nimble and emerg...

webinar
webinar

Following the recent publication of the UKs Disclosure data for 2017 I’d like to invite you to attend a very special free webinar event with me at 1pm on the 19...

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thermo-fisher-banner

Get greater structural insight into your drug product with our biopharmaceutical protein characterization workflows

Covance webinar social graphic
Covance webinar social graphic

In the first installment of the four-part “Trailblazer Series: Secrets for a Biotech Breakthrough” webinar series, we talk to a few entrepreneurs who’ve success...

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facebooklogo

It’s time. Your product launch is coming. Are you prepared to go face-to-face with the marketplace Our webinar, Achieving Launch Excellence: Creating a Found...

Pharma
Pharma

$398.00

This seminar will discuss what to consider and how to prepare for premarket notification 510(k) sand submit to the FDA.The speaker will walk you through how to ...

Long Term Live Imaging of Mouse Embryonic Stem Cells
Long Term Live Imaging of Mouse Embryonic Stem Cells

Nanolive is inviting to its first webinar on Stem Cells on Monday, 23rd April 2018 at 10 AM (CEST)*. Dr. Mathieu Frechin, Head of Quantitative Biology at Nan...

Webp.net-compress-image (1)
Webp.net-compress-image (1)

$218.00

In FDA-regulated industry, it is imperative that firms should be well aware of recent policy changes and understand what laws and regulations apply for FDA-regu...

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new-logo-2

Instrumental liquid chromatography, either as HPLC or UPLC, are common techniques in laboratories that do regulatory-compliance work. For Good Laboratory Practi...

course-serialization
course-serialization

$299.00

As counterfeit drugs have become more sophisticated, the risk of knock-offs reaching patients increases every year. Naturally, counterfeit drugs can harm brand ...

Computer code
Computer code

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer ...

Woman working on machinery in assembly line
Woman working on machinery in assembly line

$185.00

The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.

Man at computer in office
Man at computer in office

This course addresses how to write effective correspondence, reports, SOPs, and protocols in support of your company's activities.

FDAs Medical Device Clinical Trials Program
FDAs Medical Device Clinical Trials Program

$150.00

Overview: The topic is device clinical trials. This term refers to the use of medical products on/in humans, in order to gain useful knowledge about the ...

Medical Device Hazard Analysis Following ISO 14971
Medical Device Hazard Analysis Following ISO 14971

$150.00

Overview: The US FDA expects that as part of a product development Design Control Program risk management will be conducted. FDA recommends using ISO 14971 a...

Laboratory-Developed Tests
Laboratory-Developed Tests

$150.00

Overview: This presentation will review the legal definition of medical device, and how it is applied by FDA to in vitro diagnostic tests. It will review the h...

Medical Device Engineering Change Control
Medical Device Engineering Change Control

$150.00

Overview: This webinar will describe a system, based on the regulations and practical experience that will allow for efficient control of the change proc...

Validation Master Planning and Regulatory Expectations
Validation Master Planning and Regulatory Expectations

$150.00

Overview: This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System...

Laboratory Accreditation Getting There is Just the Beginning
Laboratory Accreditation Getting There is Just the Beginning

$150.00

Overview: Accreditation is not a guarantee of analytical competency. Getting accredited is just the beginning. The journey begins with defining the labor...

Combination Products Registration
Combination Products Registration

$150.00

Overview: During this introductory session, delegates will gain a complete guide to the status and impact of the latest guidelines for combination products...

ICH Q11- API Manufacturing
ICH Q11- API Manufacturing

$150.00

Overview: This webinar will address approaches to developing and understanding the manufacturing process for a drug substance. The information obtained will en...

Strategies for Billing Medicare For DME-From getting DME PTAN to Full Accreditation
Strategies for Billing Medicare For DME-From getting DME PTAN to Full Accreditation

$150.00

Overview: Learn how to provide your Medicare patients with Durable Medical Equipment to maximize patient clinical outcomes while developing a great revenue str...

The new EU Clinical Trial regulation
The new EU Clinical Trial regulation

$150.00

Overview: Transition between Directive 2001/20/EC and Regulation EU No 536/2014 Until the Clinical Trials Regulation EU No will become applicable, all clini...

Steam Sterilization Microbiology and Autoclave Performance Qualification
Steam Sterilization Microbiology and Autoclave Performance Qualification

$150.00

Overview: Successful autoclave Performance Qualification starts with a fundamental understanding of steam sterilization microbiology. Why should you Attend:...

Packaging and Labelling for Commercial and Clinical Products
Packaging and Labelling for Commercial and Clinical Products

$150.00

Overview: The program will review how to establish an effective artwork change management and approval system, including real-life examples of system success...

Preparation for GMP Inspections by Regulatory Agencies
Preparation for GMP Inspections by Regulatory Agencies

$150.00

Overview: This webinar will provide practical tips and advice for ensuring that all inspections are conducted in the most effective and efficient way possibl...

10 New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods 2017
10 New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods 2017

$1,295.00

Course "New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods" has been pre-approved by RAPS as eligible for up to 12 credits towards a pa...

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