Join the QS World MBA Tour for your opportunity to meet with admissions directors and alumni. For over 25 years, QS has been connecting prospective candidates just like you...

DESCRIPTION Please join Chewy and She+ Geeks Out at their beautiful offices in Boston for a fun night of learning, networking, eating and drinking! You’ll walk away with more...

Description This hands-on seminar provides a comprehensive approach to learning how to proactively prevent non-compliance. There will be intensive reviews on the negative...

Description This hands-on seminar provides a comprehensive approach to learning how to proactively prevent non-compliance. There will be intensive reviews on the negative...

Course “FDA Penalties for Regulatory Non-Compliance in the Pharmaceuticals Industry - 2021 in Review“ has been Pre-approved by RAPS as eligible for up to 12 credits towards a...

Overview: This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing. Why should you Attend: Testing...

Overview: It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device...

You may have heard about unconscious or implicit bias, but aren’t quite sure what it is or have a rudimentary understanding of it. At its core, unconscious bias is just what it...

The Event: Think you're up for the challenge? Check out this unique, one-day-only puzzle event where you'll be competing against 20 other teams to see if you and your...

Overview: You'll learn about the various computer system validation deliverables and how to document them through the entire process. You will learn about what must be done to...

Overview A Risk Evaluation and Mitigation Strategy (REMS) is a drug safety program that the U.S. Food and Drug Administration (FDA) can require for certain medications with...

The Event: Think you're up for the challenge? Check out this unique, one-day-only puzzle event where you'll be competing against 20 other teams to see if you and your...

Canadabiz website serves Internet users with the most accurate business information available online. Now we decided to expand and prepared a set of practical workshops...

Overview: It gets you on the right track for using electronic records and signatures to greatly increase productivity and ensure compliance. Areas Covered in the Session: Which...

Overview GMP-compliance is a must for manufacturers of finished pharmaceutical products and active pharmaceutical ingredients (APIs) according to the different national...

Securing Business Critical Applications on Microsoft Azure Join us in Burlington at the Microsoft Technology Center for an interactive discussion around common deployment...

Securing Business Critical Applications on Microsoft Azure Join us in Burlington at the Microsoft Technology Center for an interactive discussion around common deployment...

Overview Personnel in the Pharmaceutical manufacturing will be asked to write and review many different documents. These documents are important, in that, it will be scrutinized...

Course “Analytical Methods Validation for FDA Compliance “ has been Pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full...

Overview: Learn why the single most important function of the Principal Investigator and the study conduct team is the awareness, assessment, and management of Adverse Events...

Overview: It is easy to document what process has been performed, what has been investigated or changed or why something is a risk, but the difficult part is knowing how to...

Overview This training program will discuss how, in sterile compounding, aseptic technique is contributing to the prevention of microbiological contamination. It provides...

Overview With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding...

Overview: The APIs covered in this guidance document include new chemical entities and APIs of biological origin and those created by biotech processes. Why should you Attend:...

As scientific breakthroughs and novel discoveries reveal the causal link and interface between metabolic pathways and immune cell function, the inaugural Immunometabolism Drug...

Overview: You will understand how to identify, evaluate and also how to implement specific risk based techniques for risk management used in clinical trials. Areas Covered in...

Overview: This webinar will address the four key steps to compliance by device manufacturers. Also covered will be the Final Rule's provisions to address existing FG inventory,...

Overview After attending this course, you will understand data governance as a quality control discipline for assessing, managing, using, improving, monitoring, maintaining, and...

Overview: This ISO 13485:2021 webinar is a standard for Quality Management Systems of medical device manufacturers and suppliers, and is used worldwide for developing and...

Overview After attending this course, you will understand data governance as a quality control discipline for assessing, managing, using, improving, monitoring, maintaining, and...