COMPLIANT. EFFECTIVE. EFFICIENT.
In a globally regulated life science industry, PathWise provides proven methodologies in quality and compliance through hands-on and practical solutions that ensure compliant, effective, and efficient quality systems.
Developing a systematic, compliant approach to current Good Manufacturing Practices (cGMP) and 21 CFR parts 210 & 211 isn’t easy. PathWise provides tools, systems, and best practices to simplify regulatory compliance for Pharmaceutical companies and helps eliminate OOS investigations and other deviations.
Biologic and biotechnology regulations are becoming increasingly rigid, and having the right support to understand and comply with 21 CFR parts 600, 601, and 610 can make all the difference. Find out how PathWise can help your organization meet and exceed the necessary standards for your business success.