Overview: We will cover the importance of maintaining the documentation from every computer system validation effort in a "current" state. The system must be maintained in a...

Overview: The food home delivery business is exploding. While most companies and consumers have never worried about food safety when ordering Pizza or Chinese foods by...

Overview Expense reimbursement fraud—encompassing the myriad forms of employee travel and entertainment (T&E) schemes as well as Purchasing Card (P-Card) fraud—costs...

Overview This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn...

Overview This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers. Learn...

Overview The FDA released a new draft guidance document in October 2021 on the topic of efficacy and risk information in direct-to-consumer promotional labeling and...

Join MIT Technology Review on the MIT campus this May for the Business of Blockchain 2021. Held in collaboration with the Digital Currency Initiative the one-day event will...

Join MIT Technology Review on the MIT campus this May for the Business of Blockchain 2021. Held in collaboration with the Digital Currency Initiative the one-day event will...

As our lives become hyper-connected and customer expectations increase, the imperative on insurance carriers to deliver automated services with a 360 customer view is...

Good Documentation Practice and Record Keeping Regulations (FDA & EMA) Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the...

Overview: In this webinar would apply to computerized systems that create source documents (electronic records) that satisfy the requirements in 21 CFR 312.62(b) and 812. Areas...

Overview: Auditing analytical laboratories can be complex because of the preparation that is often required. All of the GMP rules do not apply to the laboratory; while there may...

Time is Money. There are a variety of direct costs to the organization associated with poorly managed conflict, including, in the worst cases, the loss of customers and good...

This training will explain the main principles behind a QbD approach and provide guidelines in how to implement the concepts into a pharmaceutical development organization....

Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacture, testing, distribution and management of a product...

Overiview A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA cannot regulate component suppliers, it...

Overview Importers and exporters must know how to classify their products. Failure to do so, can result in costly fines and penalties. Importers must understand commodity...

Get ready to move with the digital innovators of ASICS—striving to make their brand the most helpful in the eyes of their consumers. ASICS’ goal is to build innovative digital...

Featuring Alan Morinis, author of Everyday Holiness and more, Rabbi David Jaffe, author of Changing the World from the Inside Out, Rabbi Marcia Plumb, and experienced Mussar...

Featuring Alan Morinis, author of Everyday Holiness and more, Rabbi David Jaffe, author of Changing the World from the Inside Out, Rabbi Marcia Plumb, and experienced Mussar...

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Raw material requirements in a cGMP environment are often overlooked as a Company...

Overview This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted applications. It explains...

The course is designed to provide hands on training in the management of normal and complicated deliveries. This course is designed to help providers manage the high risk, low...

With 22+ hours of content, 2 interactive workshops and over 5 hours of networking with key industry leaders, this comprehensive conference will completely focus on allogeneic...

Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human...

Reducing turnover and fast-tracking new employees to productivity is a key business imperative. The reality is that about 30% of employees don’t make it past their first year...

The European Parliament just adopted the Medical Devices (MDR) and In vitro Diagnostic Medical Devices (IVDR) regulations. The adoption marks another hallmark event in the...

Overview Learning Management Systems (LMSs) are important tools for assuring and demonstrating that Pharma employees maintain their training, and their GMP compliance, up to...

Overview The basic provisions of privacy for protected health information are well known. HIPAA has been around more than a dozen years. HIPAA privacy rules serve to protect...

Overview Learning Management Systems (LMSs) are important tools for assuring and demonstrating that Pharma employees maintain their training, and their GMP compliance, up to...