Well, you can spend $10 to do a number of things. You can have a cup of coffee for you and your friend. You can buy an ice-cream each to two of your kids. You could buy them a couple of comic books. Or, you could choose to grow up in your profession. Wait a minute. Is there something wrong with the last of these options? Growing up in one’s profession? For $10? Yes, you are reading this right. It is neither a typo nor the height of exaggeration. Growing up in one’s career by enrolling for an FDA, medical device or pharmaceutical course for $ 10 each is a possibility. In this place and time. GlobalCompliancePanel, a leading provider of professional trainings for all the areas of regulatory compliance, makes this possible!
Want to confirm if this is true? Please log on to GlobalCompliancePanel’s website to check on the dozens of recorded webinars that are available for all of $10. The original cost of these webinars is $ 265. So, what does this mean? It means that you have a jaw-dropping discount of 95% on each of these FDA, medical device or pharmaceutical courses. Can anything be sweeter to hear for a Regulatory Affairs professional?
From the time it started training professionals in the areas of regulatory compliance, GlobalCompliancePanel has been fired by the zeal for taking these training courses to a wider audience of regulatory compliance professionals. It has been training professionals in all the areas of regulatory compliance to help them get on par with the times and the changes that keep happening in their professions.
This is the latest endeavor from this well-known provider of professional trainings for the regulatory compliance areas. These courses are designed to help regulatory professionals take important steps towards scaling up in their professions and meet the regulatory demands set out by the regulatory agencies.
A look at some of these webinars:
FDA inspections are considered one of the most delicate tasks a professional in the regulated industries can come across. This course from GlobalCompliancePanel teaches participants just what they need to do when an FDA inspection happens at their facility.
Medical device companies are up against a slew of regulations from the FDA, EMA, and other regulatory agencies. They cannot get any of these wrong, if they have to meet the requirements and market their products and stay in the market. At this course, GlobalCompliancePanel equips them with everything they need to understand about the European Union released directive 2007/47/EC (amending Council Directive 90/385/EEC).
Harmonization with the ICH-Q10 is very essential for a pharmaceutical company’s Quality System. The FDA aims to promote a pharmaceutical Quality System to build on the 21 CFR 820 it formulated in 1996. Participants can gain complete understanding of this topic by enrolling for this webinar from GlobalCompliancePanel.
Sign up today! This is an opportunity you cannot afford to miss!