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Life Sciences Document Services

 

How can time-to-market costs stay down while the process becomes more efficient?

 

The challenge of developing and marketing new products in an industry that is highly regulated is a daunting task. From this process, thousands of documents are produced in order to stay in compliance with these rigid regulations that the Food and Drug Administration (FDA) places on the biotechnology, biopharmaceutical, and medical supply companies. 

• Significantly reduce costs associated with the processing, transporting, and storing documents.
• Secure storage and capture process of all file formats, including bound lab books
  
  

We differentiate ourselves from our competition by becoming highly involved the content management process from the early stages of Phase I of Clinical Research & Development. As a process that may take anywhere from 2 to 10 years, R&D will generate a great deal of documentation that proves burdensome to scientists and regulatory agencies. With a recommended 3 FDA meetings throughout the R&D and NDA Review process, both parties are pressured to make the submittal process efficient. The process will be efficient with Merritt Scanning Technology Solutions in place.

 

 

Joseph Merritt & Company is an authorized reseller of the Adobe® line of products.  For product purchase or more information, please contact us with your inquiry.

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If your company or organization falls within the life sciences realm, have your document scanning done by Joseph Merritt. Why us? Specializing in life sciences document scanning, we work with you from the early stages of content management for Phase I of Clinical Research and Development, and understand that this process can take from two to 10 years and can generate extensive documentation. As your company or organization may need thousands of documents for FDA compliance, we have the ability to scan all file formats, including bound lab books, and streamline the submission process for both scientists and regulatory agencies.