Clarity puts FDA regulations management at the core of its processes with workflow tools tools, document tracking, and process features. Being crafted specifically for FDA regulated manufacturers on QuickBooks, Clarity make compliance easy by integrating it into your existing manufacturing process.
Clarity solutions help you track and monitor product specifications at every step of your manufacturing process. From comparing actual test results against spec limits to calculating potency and scaled batches Clarity helps you maintain your specifications.
Try as one might, things don't always go according to plan.
Clarity's suite of features helps you make better, faster decisions when things go awry whether they're caught during production or at packaging and distribution.
Clarity helps you track potency, ingredients, weights and more so that if you need to make a substitution or a distillation is slightly off you know whether you can still meet your specifications.
Clarity helps you track every specification from ingredient to packaging to make sure you are compliant. With powerful reporting and comparison tools you'll know when something's amiss.
Clarity's document management solutions help you record your deviations and possible CAPA's. With smart document linking features organization is made simple and finding the information in the future is quick and easy.
Certificates and Validations
Maintain and catalogue certifications for all of your products and incoming ingredients.
Keep up with vendor certifications with renewal alerts.
Track important validations and lab results for things like quality and potency.
Create holds and checkpoints at critical control points along your production cycle. Our web app allows anyone anywhere to conduct validations and signoffs to minimize downtime and ensure quality.
Inspections and QC Holds
Integral to Clarity's entire solution set is quality control. We believe that quality should be built into the same process as the rest of production and operations.
With mobile features and cloud based applications Clarity helps you streamline the incoming inspection process. Inspect, compare, and validate right from the shop floor. Ingredients wont be approved for allocation until the product is verified by quality control.
21 CFR Part 11 Compliance
21 CFR Part 11 is are the FDA's regulations on electronic records and electronic signatures.
Permissions based accessibility and digital sign-offs make Clarity solutions entirely compliant with the FDA's 21 CFR Part 11. Save time and do the right thing with Clarity.
Every business is different. Tell us about yours.
Clarity is compatible with any FDA regulated industry running QuickBooks or Acctivate. Let us help you craft a personalized, comprehensive manufacturing solution.