BLOG The Elements of a Successful CAPA Process To date, the most widely-used and effective process for ensuring safety and quality management is a closed-loop corrective action and preventive action system (CAPA). Learn more
BLOG How Pharmaceutical Quality Drives Performance While many pharmaceutical and biotech companies have begun investing in their quality systems, it’s not uncommon to still find mid-size or emerging manufacturers manually entering data into spreadsheets or using siloed systems that are unable to share information electronically. Learn more
BLOG The Power of Integration: A Holistic Approach to Quality and Document Management One of the key components for Life Sciences companies is to have their documents and data in order.... Learn more
BLOG It’s Time For The Life Sciences Industry To Embrace Quality 4.0 Sparta’s President and CEO, Oxana Karpenko Pickeral, explores how the Life Sciences industry can address core challenges and connect the “data dots” by embracing Quality 4.0. Learn more
BLOG 3 Ways the CAPA Process is Like Preparing for the Big Game What do football and corrective and preventive action (CAPA) have in common? More than you may think. As... Learn more
BLOG 5 Ways Technology Meets the Challenges of Complaint Handling Technology can play an important role in addressing the challenges of complaint handling in regulated industries, such as... Learn more
BLOG Integrated Document Management: Leveraging Technology to Improve Compliance and Efficiency Quality is essential for manufacturers in regulated industries, such as Life Sciences, to ensure the safety and efficacy... Learn more
BLOG Document Management: Communication with Regulators Document management technology can be used by manufacturers in regulated industries, such as Life Sciences, to aid their... Learn more
BLOG Document Management: A Tale of Two Manufacturers Experiences from two TrackWise Digital customers, Arbor Pharmaceuticals and Mikart, Inc., highlight the challenges that companies can face... Learn more