Pharmaceutical and Life Sciences

Marco’s document management solutions help pharmaceutical and life sciences companies such as biotechnology firms, medical device manufacturers and clinical research organizations, manage critical processes and paper and electronic records to ensure compliance with regulations and standards, such as FDA 21 CFR Part 11. With a detailed audit trail of all document activity, you’ll ensure compliance with such standards, and benefit from an efficient and secure workplace.

Features and benefits for your Pharmaceutical and Life Sciences firm:

• Ensure compliance with regulations such as FDA 21 CFR Part 11.
• Organize and index documents by project, discipline, customer or client, or other criteria.
• Search and retrieve documents instantly by typing in a tag or keyword or two, or by searching on a word in the document using "full-text" search.
• Automate review and approval processes for offers, contracts, disclosures, and other important real estate documents.
• Efficiently manage and track emails and scanned paper documents.

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