Our Process

The following flowchart illustrates Cytophil’s capabilities to move your idea from infant stage to a final marketable product.

 Your idea for a medical device > conduct market needs assessment > product development phase > includes shelf life testing chemical testing physical testing mechanical testing and preclinical trials > leading to pilot production > validation and verification by quality assurance is required > regulatory approval sometimes requires preparation of products for clinical trials > market development preps for release of product to market > before full manufacturing contract manufacturing can take place > then you have a marketable product

Click here to see more detailed descriptions of any of the above services.

Doc# 02meddevicecomprocess Rev# 00 Approval date 10-04-11