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The productivity of any company is almost fully dependent on the quality of its manufactured goods. Pharmaceutical and medical device manufacturers are no exception to this. Occasionally, problems do arise, either of a regulatory nature or with quality standards that do not meet specific requirements. Both of these factors can often be traced back to human error - in fact, human generated mistakes pose the greatest risk to product quality with the result that significant monetary losses to investors, stockholders, and society in general, can be incurred through expensive product recalls, replacement, or withdrawal from the market.
The incidence and effects of human error can be significantly reduced through the introduction of meaningful competency training programs.
The increasing emphasis given today towards e-training, or computer based competency training, demonstrates its growing importance and acceptance as an adjunct to the traditional education base. Some of the immediate advantages, particularly within FDA regulated industries, are;
- On-site training
- Just in-time training when you need it
- Instructors are not required
- Training can be repeated on demand
- Content control and administration
- 21 CFR Part 11 compliant
CACTUS is a company-wide, competency training solution package. It features 21 CFR Part 11 compliant solutions for your entire competency training management requirements, all of which can be scaled and optimized for use in fully automated, semi-automated, manual, and hybrid operations.
CACTUS is the total solution for your entire competency training needs. By utilizing CACTUS for your competency management and validation requirements, not only will it assist you to be compliant with the provisions of 21 CFR Part 11, it will also motivate your staff to fully utilize their training opportunities to the fullest, the benefits of which will be felt immediately.