You have just received an FDA Warning Letter or 483, what do you do next?

Did you just get issued a FDA Warning Letter or 483? Are you a Pharmaceutical, Medical Device or Biotechnology company? Here are steps to take after you receive a FDA warning letter or 483 that will aid in the success of your remediation effort.

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5 Tips to Save You Time When Doing a Remediation Effort!

Are you finding that your remediation project is a more complex process than anticipated? Are you a Medical Device, Pharmaceutical or Biotechnology company? Read the top 5 things to avoid during a remediation effort that will save you a lot of time and trouble.

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Tips to a Successful Remediation

In this webinar, you will learn about the three most common mistakes made throughout remediation efforts that can cause a company to miss the objective as a whole, as well as how to properly organize your remediation team to successfully reach the standards of patient and product safety. Ensure your current or future project runs smoothly and successfully by implementing the tips to a successful remediation.

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3 Steps for a Successful HANA Implementation

Ensure your current or future HANA project runs smoothly and gain access to these insider steps! Experienced SAP consulting experts will outline a systematic approach for implementing SAP HANA. Hear the inside scoop of what to really expect and how to best prepare for your HANA project.

This LIVE webinar will cover:

  1. Project Planning
  2. Migration of BW to HANA
  3. Optimization of HANA and Efficient Reporting

Don’t miss the opportunity to gain valuable insight into one of the most talked about developments in the industry.

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Top 5 Benefits of Using Epic Caboodle

In this eBook, you will hear from our Epic Caboodle expert Christopher Kaufman about the top 5 benefits of Caboodle and why you should use it!

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5 Important Factors of the New MDR Classification Requirements for Medical Devices

In this eBook, you will learn 5 important factors of the new MDR Classification Requirements specific to Medical Devices from a Regulatory expert, Sequita Lindsey.

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