Navigating the complex landscape of regulatory compliance and staying updated with the latest good manufacturing practices (GMP) standards is a large task for life science companies. Ensuring readiness for global regulatory inspections and maintaining operational efficiency while regulations are evolving adds to the challenge.
At Epista Life Science, we specialize in providing comprehensive GMP Training and Audit Services tailored to the Life Sciences industry. Our programs are designed to ensure your team is up to date with the latest in good manufacturing practices and prepared for audit.
From customized, practical training courses to in-depth audit services spanning GMP, GDP, and ISO13485/MDSAP, we empower your organization to optimize business efficiency while maintaining the highest standards of compliance. Whether you're looking to enhance your team's skills, prepare for regulatory inspections, or ensure your quality management systems are without fault, Epista is your partner.
We are dedicated to advancing the standards of good manufacturing practices (GMP) through comprehensive training programs. Our courses are meticulously crafted to meet the dynamic needs of the pharmaceutical and active pharmaceutical ingredient industries, focusing on practical applications and current regulations.
Our Training services include:
Our audit services are built on a foundation of extensive global experience, including over 100 audits in the realms of Drug Substance, Drug Product, and Medical Devices. We specialize in GMP, GDP, and ISO 13485/MDSAP audits, offering unparalleled insights and compliance solutions.
Our services include:
We enjoy sharing our knowledge. Get in touch to find out how Epista can add value to your Life Science company.
