In the highly-regulated pharmaceutical and nutraceutical industries, not only can being out of compliance result in severe financial sanctions, it can also permanently put you out of business.
This is why proper validation and documentation of your systems and operations is vital to your business. And now, 21 CFR Part 11 Electronic Records; Electronic Signatures is regaining focus with FDA and other regulatory inspectors. Do your in-house resources have the time and the training to satisfy these regulations?
If you are an Equipment or System Manufacturer, your Life Sciences customers will be looking to you to provide them with the documentation they require. Providing specialized documentation is becoming a requirement for making the sale. You cannot afford to fall behind by not providing adequate documentation that satisfies the requirements of 21 CFR Part 11 or other regulations.
Tanis Technical can help. Our experts provide services that help our customers increase compliance, sales, and internal control and efficiency of business and manufacturing processes and documentation while achieving superior ROI from their technology investment.
Read how a Validation contractor can help...
Read about the vital services we provide to both Life Sciences companies and Equipment/System Manufacturers:
