Course description
Documentation Simplification
Has your paperwork grown organically over the years? Have you added extra checks, extra fields and immense numbers of signatures in response to deviations and yet still find the same issues, or similar, repeat themselves? This pharmaceutical training workshop will provide you with practical tools to help you maximize the potential of your operation by significantly simplifying your documentation and the content of procedures. This will improve the design of batch manufacturing/packaging records.
Upcoming start dates
Suitability - Who should attend?
Is your team performing badly on right first time metrics? Is your management team increasingly concerned as more companies are facing data integrity problems than ever before?
From warehousing to quality this course is ideal for any individual/department who is responsible for documents that are too long, too complicated and result in poorly completed records.
Improve the understanding of your issued instructions, the format that you provide for the record to be completed in and consequently improve your documentation right first time.
Outcome / Qualification etc.
Key Learning Objectives
Do your documents contain inherent risks, error traps or ambiguity? Do they contain over-complexity, poor instructions or inadequate recording space? These issues can lead to deviations and potential batch losses. You need to simplify your documents, and this course is designed to show you how.
Upon completion of this course, delegates will:
- Know the causes of complexity and how to measure it
- Know the regulatory expectations on good documentation practices and recent deficiencies in this area
- Learn the process to simplify records, procedures and batch documentation
- Learn best industry practices and drive out complexity
- Understand data integrity implications when completing documentation
There are also opportunities for discussion throughout the workshop, as well as real-life case study presentations.
Course delivery details
If you choose our virtual learning option, training will be delivered via a combination of an instructor-led virtual classroom and self-paced learning online. Full details will be sent to you following registration.
All of NSF's pharmaceutical training courses can be brought on-site, tailored to your key concerns and delivered at a time that suits you.
Why choose NSF International, Health Sciences
Trained over 1,300 delegates on our CQI and IRCA certified GMP PQS lead auditor training course
Provided expert health sciences training for over 30 years
More people have become ‘Qualified Persons’ in Europe through our training programme than any other training provider
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Reviews
Average rating 4.5
I now have more clear understanding how to go about BMR/SOP simplification.
Expenses
Discounts
Discounts offered to NHS staff, regulators and charities.
Excellent communication throughout today, I was very impressed. I will be communicating back to the laboratory all that I have learned today and recommending your work to them. ...