Displaying 1–25 of 57 results for Vaisala
When is Empty Chamber Mapping a Worst Case Scenario Equipment Qualification?
And what about thermocouple accuracy?
How do you determine the frequency of environmental monitoring, validation and revalidation?
When you have two monitoring systems working in parallel -- a main monitoring system and a redundant
USP  assigns "specific responsibility" to the manufacturer. In the case of contract
eBook on meeting USP and EU GDP regulatory requirements. Learn the latest revisions from the U.S. Pharmacopeial Convention (USP) Good Distribution Practices (GDP) according to the European Commission.
Effective, compliant cleanroom humidity control hinges on careful sensor management
This eBook includes calibration pitfalls, tools, and best practices for sensing instruments in GxP-compliant environments.
The FDA mandates the validation of environmental conditions that can affect the strength, identity, safety, quality, and purity of pharmaceuticals, medical devices, or biologics.
Learn how to use GAMP methodology to select and validate a monitoring system software.
Vaisala recommends a 9-point process for successfully validating a GDP compliant warehouse or other storage space.
A handy guide to FDA compliance terms
We polled pharma fans to pick their MVPS (Most Valuable Products) from the industry's top tech teams
Humidity Measurement: The Devil is in the Details
A 9-Point Plan for GxP Warehouse Mapping
Validation FAQs - Five Key Questions You Need to Have Answered in Planning a Validation Project
Thermistors and Thermocouples: Matching the Tool to the Task in Thermal Validation
Matching Environmental Monitoring & Mapping to FDA/ICH Guidance for Better Stability Studies
Qualifying Cold Chains, Writing Performance Qualifications and the Parenteral Drug Association Technical Report 39
viewLinc Monitoring, Alarming & Reporting software
HMT140 Wireless Logger