WEBINARS

 

Compliance Training Webinars for Regulated Industries

FDA Regulatory Inspection and Audit Training: Pack of 6 Training Courses

webinar-speaker   Susanne Manz,Joy McElroy,Charles H Paul,Loren Gelber,Martin Lessem,Stephen Schwartz

webinar-time   7 Hrs

Product Id: 706482

Recording Available

* Per Attendee $999

 

Pharmaceutical Data Integrity Success Training Kit - Pack of 8 Training Courses

webinar-speaker   Gregory Martin,Kelly Thomas,Mark Powell,Ron Snee

webinar-time   11 Hrs

Product Id: 706481

Recording Available

* Per Attendee $1299

 

Overcoming Obstacles of The Canadian Drug Regulatory Landscape

webinar-speaker   Susanne Picard

webinar-time   60 Min

Product Id: 706188

The Canadian Drug Approval Process is misunderstood by many and considered harsh by some. We will explore reasons why the Canadian market should not be overlooked and the benefits of including Canada in strategic drug development initiatives. We will share insights and practical examples that facilitate a positive, proactive and transparent interaction with Health Canada, and provide strategies for avoiding obstacles and managing them efficiently should they occur.

Recording Available

 

Validation of HPLC/UPLC Methodologies

webinar-speaker   John Fetzer

webinar-time   60 Min

Product Id: 705291

This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.

Recording Available

* Per Attendee $249

 

Coronavirus: Health and Business Considerations

webinar-speaker   William Levinson

webinar-time  

Product Id: 706434

The coronavirus outbreak has caused thousands of deaths around the world along with extensive economic disruption. China has issued several overt threats to disrupt U.S. supply chains, and the stock market is in turmoil. This presentation will provide information on how organizations can position themselves to handle the disruption and even realize opportunities for improved performance as a result.

Recording Available

 

Human Error Prevention Training Kit

webinar-speaker   Ginette M Collazo,Tom Kramer,John E Lincoln

webinar-time   10 Hrs

Product Id: 706472

Recording Available

* Per Attendee $1299

 

Change Management - Managing Effective Change and Eliminating Unwanted Changes

webinar-speaker   David Husman

webinar-time   90 Min

Product Id: 706420

Change Management is one of the most critical quality systems a company can have. Well managed systems are effective in implementing desired changes and preventing unwanted modifications to validated processes. This webinar will discuss the requirements for change management, the steps for effective change management and the actions companies can take to ensure unwanted changes do not occur in their operations.

Recording Available

 

Beyond the Box-Checking: Strategies for Diversifying Your Ongoing GMP Training

webinar-speaker   Mike Kent

webinar-time   60 Min

Product Id: 706329

This webinar will illustrate ways to take your ongoing or refresher GMP training to well beyond recycling existing content, regardless of your training budget or available resources. By asking a few simple questions of key stakeholders, and tapping into your already creative process, annual GMP training can start to become more than just something everyone has to complete. Come away with a plan to take your program beyond a year-end box-checking exercise and into a resource that people flock towards.

Recording Available

 

Global Food Additive Regulation Review: Headwinds and Opportunities

webinar-speaker   Carolyn Fisher

webinar-time   90 Min

Product Id: 706290

This webinar will start with a general background about global regulations and then go into detail about specific food additives and how the regulations vary in specific international, regional regulatory and country regulatory documents.

Recording Available

 

PAT (Process Analytical Technology): An FDA and Industry Effort

webinar-speaker   Nissan Cohen

webinar-time   90 Min

Product Id: 706370

Process Analytical Technology was released by the FDA as a 21st century guideline in September 2004. This guidance was released to help the pharmaceutical industry with real-time release, process understanding, and using the process to ensure all CPPs and CQAs meet compliance, URS, and SOPs. The use of PAT can alleviate strenuous validation procedures by using the process as the function of validation.

Recording Available

 

Basic Laboratory Skills

webinar-speaker   Mark Powell

webinar-time   60 Min

Product Id: 706286

Accurate measurement of weight and correct use of volumetric apparatus are prerequisites for valid analytical measurement. This webinar covers the quality-critical aspects of both. It is intended for new starters in industrial analytical laboratories or for other staff who would benefit from refresher training.

Recording Available

 

Human Centric Change Management

webinar-speaker   Madonna Swanson

webinar-time   60 Min

Product Id: 706388

Change is difficult. At the core of all change is human nature and human nature is as diverse as each individual. Learn proven techniques that enable your transformation to not only be effective, but embraced by the diverse individuals in your organization.

Recording Available

 

Recording Available

* Per Attendee $999

 

Recording Available

* Per Attendee $1099

 

Handling a Chaotic Work Environment: How to Prioritize Work and Make Good Decisions Under Pressure

webinar-speaker   Christopher R DeVany

webinar-time   90 Min

Product Id: 706342

This highly interactive Webinar offers you and your team an array of practical tools to help you get things done in today's chaotic and constantly changing work environment. You’ll learn practical techniques for making structured decisions—even under pressure—to earn buy-in from bosses, coworkers and customers. In a workshop environment, you will participate in valuable exercises utilizing real-world case studies. You'll emerge with an action plan you can use right away to master expanding workloads and complex decisions.

Recording Available

 

Effective Vendor Risk Management

webinar-speaker   Mario Mosse

webinar-time   90 Min

Product Id: 705193

Vendor risk management is an important component of a financial institution’s operational risk management program. This training program will examine how a sound vendor risk management program, including careful planning, due diligence and selection, and close oversight and monitoring during the life of the contract, is necessary to reduce the risks posed by the outsourcing of critical functions.

Recording Available

* Per Attendee $229

 

Cleaning Validation Made Easy : Basic Concepts of Cleaning Validation

webinar-speaker   Victor Olatundun

webinar-time   60 Min

Product Id: 706346

This webinar will discuss the basic concepts associated with cleaning validation to facilitate the construction of robust cleaning validation program as well as provide a cost-effective approach on conducting cleaning validation.

Recording Available

 

FDA's Deeming Regulations for e-Cigarettes, Cigars, and other Tobacco-related Products

webinar-speaker   Carolyn Troiano

webinar-time   90 Min

Product Id: 705097

This webinar is intended for those working in the FDA-regulated tobacco and related industries, including e-liquids (vapor), e-cigarettes, cigars, and smokeless tobacco products. Functions that are applicable include research and development, manufacturing, Quality Control, distribution, clinical testing and management, adverse events management and post-marketing surveillance. You should attend this webinar if you are responsible for planning, executing or managing the implementation of any system governed by FDA regulations, or if you are maintaining or supporting such a system.

Recording Available

* Per Attendee $299

 

Preventing Harassment, Abusive Behavior, Bullying and Discrimination in the workplace (for staff)

webinar-speaker   ArLyne Diamond

webinar-time   120 Min

Product Id: 706319

It only takes two people to have a behavior reported as either sexual harassment, bullying, or discrimination. Thus, we strongly recommend that you provide training to all employees at least annually no matter how many you consider your head count. This course is mandatory for managers and supervisors in companies having 50 or 15 or more employees. In California it has now changed to five (5) or more and other states will follow.

Recording Available

 

Overview of IVD Regulations in the US, EU and Canada

webinar-speaker   Josh Levin

webinar-time   90 Min

Product Id: 706382

This webinar will present an overview of the regulation of in vitro diagnostic (IVD) devices in the United States, European Union and Canada. With a primary focus on IVD regulation by the US FDA, the webinar will cover the classification of IVD devices, an overview of data required for different submission types, and special topics. The webinar will also cover the changes in regulatory oversight in the European Union, and will briefly touch on the regulation of devices in Canada, including recent changes related to oversight of the quality system in that country.

Recording Available

* Per Attendee $299

 

 

 

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