Our mission as a contract manufacturing company is to solve the challenges of start-up product scaling and process development and to provide customers with next-level communication, expert guidance, and laboratory testing service speed with excellence. MycoScience is the logical choice for pharmaceutical contract manufacturing and laboratory testing.
We bring a wealth of experience having over 30 years in the medical device and allied industries. We specialize in environmentally controlled, low volume, clinical production of diagnostics, pharmaceuticals and medical devices. We perform a variety of laboratory regulatory tests including cleaning validation, preservative efficacy testing, microbial challenge testing and more.
We bring a wealth of experience having over 30 years in the medical device and allied industries. We specialize in environmentally controlled, low volume, clinical production of diagnostics, pharmaceuticals and medical devices. We perform a variety of laboratory regulatory tests including cleaning validation, preservative efficacy testing, microbial challenge testing and more.
Services
MycoScience is an ISO 13485:2016 certified contract manufacturing organization specializing in syringe and vial filling of gels and highly viscous materials for medical device and pharmaceutical applications. We also perform a variety of regulatory testing services with expertise in supporting unique product families getting to clinical trials efficiently.
Mycoscience specializes in contract manufacturing services and R&D process for the pharmaceutical industry. We also perform a variety of regulatory testing services in microbiology, EO residuals, cleaning validation, bioburden, accelerated aging and package integrity for medical device and allied industries.
We offer you competitive prices for simple routine testing, prompt communication regarding test status and results, and experience with regulatory and biocompatibility testing services for unique product families. Learn what cleaning validation is and the top three cleaning processes that must be validated to keep your medical device or medical product sterile.
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