GMP compliance and inspection readiness are recognized as essential for maintaining a business's license to operate within Life Sciences.
At Epista, efforts are concentrated on enhancing the competency and expertise of individuals and specific teams such as QA, QC, QP, auditors, management, validation and equipment responsible within pharmaceutical, biotechnology, and medical device companies through specialized training programs.
Offerings include online courses, on-site training, and customized solutions tailored to meet specific needs.
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At Epista, our trainers and instructors are recognized industry specialists, with the majority bringing over 25+ years of (invaluable) experience in compliance, inspection readiness, and auditing.
Their extensive knowledge and practical expertise enrich every training session, guiding and empowering individuals and teams - such as QA, QC, and management - to achieve full inspection readiness and integrate compliance into their daily operations.
With the continually evolving regulatory landscape, the necessity for both onboarding and ongoing training to effectively prepare and support individuals and specialized teams is fundamental.
Employees trained in the latest standards are known to manage risks adeptly and face regulatory inspections with confidence. Furthermore, a quality-focused mindset is encouraged across all specialized areas, ensuring each role (and responsibility) upholds compliance, product quality and patient safety.