
Air Purification Product Testing
To evaluate the performance of your air purification device, we analyze changes in airborne contaminants by comparing levels detected prior to and following its operation.
“We partnered with Test Cert for shelf-life and stability testing of wound care products. Their lab follows strict quality protocols, and their reports are thorough, detailed, and accepted without question by authorities. A trusted name in the industry.”
– Dr. Nadia Zubair, Head of R&D, Dermalife Health
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Dr. Ayesha Malik

Zeeshan Rauf
FAQ
Is confidentiality guaranteed?
Yes, we maintain strict confidentiality agreements to protect your intellectual property and proprietary information throughout the testing process.
What’s the process for starting a project with TestCert?
Initial consultation
Scope definition & quotation
Sample submission
Test protocol approval
Testing & reporting
Technical support for submission (optional)
Do you offer customized testing plans?
Absolutely. We tailor testing protocols based on your device, regulatory market, and risk classification.
Can TestCert test prototypes and pre-production devices?
Absolutely. We test both prototypes and production-ready devices to help you identify issues early and ensure compliance before mass production.
What are your accreditation and certifications?
TestCert is accredited by [insert relevant accreditation bodies, e.g., ISO/IEC 17025], and our lab meets the highest quality and safety standards.
What are your pricing and payment terms?
Pricing depends on the testing scope and complexity. After initial consultation, we provide a detailed quotation. Payments terms will be shared along with the quotation.
Related tests
Medical Device Biological Evaluation Report
- ISO 10993-1 - Biological evaluation of medical devices
- Meets the requirements of FDA/MDR
- Provides comprehensive ISO 10993 report
- Completed by in-house toxicologist (competent person)
ISO 10993-23 Test for Irritation
- Good Laboratory Practice GLP study
- Biological Evaluation Plan and Report
- ISO 10993-23 - test for irritation - in vitro methods
Extractables & Leachables (E&L) Testing
- ISO 10993-18
- USP<1663>/<1664>,USP<665>/<1665>
- Aligned with MDR and FDA guidance
- Custom Extractables Stufy Design
ISO 10993-5 Cytotoxicity testing
- Good Laboratory Practice GLP study
- Biological Evaluation Plan
- Biological Evaluation Report
- ISO 10993-1 - cytotoxicity- in vitro methods
Medical Device Biocompatibility Testing
- Biological Evaluation Plan and Report
- In Vitro and InVivo methods
- Extractables and Leachables (E&L) Studies
- Also testing after cleaning, disinfection & Sterilization
Medical Device Biological Evaluation Plan
- ISO 10993-1 - Biological evaluation of medical devices
- Meets the requirements of FDA/MDR
- Provides comprehensive ISO10993 testing plan
- Completed by in-house toxicologist (competent person)