Medical Devices

What are USP Methods for Pharmaceutical Drugs?

U.S. Pharmacopeia (USP) is an organization whose main goal is to help improve human health by creating standards to ensure

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Medical Devices

3 Methods of Sterilization to Increase Sterility Assurance Level

Sterility assurance level (SAL) refers to the probability of a microorganism surviving the sterilization process, making the item non-sterile. Currently,

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Medical Devices

How is ISO 10993 Medical Device Biocompatibility Testing Performed?

ISO 10993 medical device biocompatibility testing is performed to observe how compatible a device is with living tissue. To be considered

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Medical Devices

Preclinical Drug Development

The drug development process is an iterative process. Each stage of development helps to ensure the final product is effective

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Medical Devices

NIST Technology Transfer 2016 Report

Earlier this month, the National Institute of Standards and Technology, known as NIST, published the 2016 Annual Report on Technology

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Medical Devices

Medical Device Sterilization Validation Testing

Medical Device Sterilization Validation  is imperative to invasive sterile medical products such as implants and reusable surgical instruments. ContractLaboratory.com routinely helps

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