Welcome
Don't invest in closing deviations faster, invest in preventing them.
We are your error prevention partners.
Many firms face similar challenges with high error rates, long wordy procedures, inadequate investigations or training, limited resources, and performance issues. Many are too busy for continuous improvement. Sound familiar? If so, we don’t have to accept the consequences of these issues — cost, rework, firefighting, delays, compliance risk, etc.— as part of doing business.
Our mission is to help companies do things they have to do— GxP/Quality Systems/technical training and documentation, drastically reducing errors, and improving performance—BETTER. Our solutions are transformational, shift mindsets, and involve NO new software, validation, or even change control. Partner with us.
Did you know?
At least 90% of all so-called human errors are actually due to underlying system deficiencies. Biopharm companies work in an error-prone environment with complex processes and rigorous regulatory and documentation requirements. They work with pressure, deadlines, distractions, multi-tasking, and myriad other risk factors. They require a high-performing, risk-aware workforce that understands the why's behind the how-to's and what really causes so called 'human errors.'
Why BEPA?
We partner with you to tailor effective and efficient solutions aligned to the speed of your business, that change mindsets, greatly reduce errors, improve performance and comply with regulatory requirements.
We are experts in designing and delivering highly engaging and effective training and holistic programs in:
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Human Error Prevention
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cGMP and ICH Guidance
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Investigations & CAPA
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Competency-Based Learning
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Writing Effective GxP Instructions
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Contamination Control
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Data Integrity / GDocP
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Inspection Readiness
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Change Control
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Training Program and Process Design
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Rapid Needs Analysis
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Instructional Design
Eighty-five percent of the reasons for failure are deficiencies in the systems and process, rather than the employee. The role of management is to change the process rather than badgering individuals to do better.
- W. Edwards Deming
Do you experience deviations, delays, rework, "firefighting" and documentation errors?
Many biopharm companies do. Most estimates place deviations in the $10,000/deviation range. Many Quality leaders feel this estimate is too low.
Biopharma companies continue to spend precious time, resources, and money trying to write deviations faster. With a change in approach, a small investment of resources, and a clear plan, you can reduce deviations in your firm by 50 - 70%.
We can show you how.