How to Reduce Compliance Risk? Join Now: Trainings at $10

[John Robinson]

As a regulatory professional, do you face the same jitters as thousands of your peers in the industry? Are you concerned, like many of them, about how to reduce compliance risk? Then, join now: trainings at $10!

How to reduce compliance risk is a major challenge for regulatory professionals. Whether they are experienced or are new, there is some discomfort in implementing the provisions of FDA and other agencies’ regulations, mainly because of their ambiguity and complexity. But from now on, how to reduce compliance risk will become the smallest of your worries! How? Join Now: Trainings at $10 from GlobalCompliancePanel.

GlobalCompliancePanel has trained thousands of professionals in the regulatory compliance industries. So much so, that it is today a name to reckon with in this industry. It could have been happily going about its business as usual. But being the responsible and ethical company that it is; GlobalCompliancePanel has taken the responsibility of ensuring that regulatory compliance professionals get easy and comfortable access to the hordes of courses that it has organized during the ten years of its existence. That is why it has this offer by which when you are faced with how to reduce compliance risk, all that you need to do is join now: trainings at $10!

With the FDA and other regulatory agencies such as the EMA coming up with regulations at the drop of a hat on almost every conceivable area; regulatory professionals are faced with a major challenge of how to understand, interpret and implement them. Regulatory trainings are a blessing, but let us admit it: They cost a bomb. It is here that GlobalCompliancePanel has decided to come to the rescue.

The answer to the question of how to reduce compliance risk is this: Join Now: Trainings at $10! It is the same webinars that have been imparted by our world-known experts over the years that have found their way into this offer by which how to reduce compliance risk is as simple as one can imagine: Join Now: Trainings at $10! These webinars, once purchased, can be viewed and played any number of times, for up to six months from the date of purchase. What better means to reinforce your learning!

Finding this offer too slurpy to resist? Let us give you a small taste of the feast that is to come your way:

With electronic medical records and electronic handling of study data becoming increasingly common; involving computer systems in clinical research implies knowledge of 21 CFR Part 11 (Electronic Records; Electronic Signatures). Clinicians need to have an understanding of all of the ramifications of this Part of the code. Purchase this webinar for all the answers!

Are you aware of the similarities and differences between Pharmaceutical and Medical Device Validation Guidances? Process Validation (PV) has been a widely discussed and debated phenomenon in FDA regulated industries for many years. Do you know what process validation is and how you would explain it to an “alien” from another industry? Learn more on this right here!

Developing the risk management plan involves having deep knowledge of the documentation process involving Risk Acceptability Criteria, risk review, verification activities, and information collection activities. Have all your doubts in these areas cleared here!

The FDA issued its Guidance on Process Validation in 2011. Want to understand its general principles and practices? The new requirements expand validation from a one-time activity into a full lifecycle philosophy, encompassing statistics, risk management, project management, and new technologies. This webinar is a blessing for any professional involved in process development and validation in the drug, API, or biologics industries or their vendors, and validation personnel in the medical device, tissue processing, and dietary supplement fields.

So, is there something that is holding you back? Act NOW on how to reduce compliance risk? Join now: Trainings at $10!

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