Are you an In-Vitro Diagnostics manufacturer, importer, inventors, distributor, academic institution or consumer that needs third-party laboratories for In-Vitro Diagnostics testing or R&D services? Contract Laboratory can help you with all your In-Vitro Diagnostics routine and non-routine lab analysis, product development, experiments, examinations, evaluations, inspections, certifications and research studies such as:
Contract Laboratory helps with the testing, research, product development, certification, and inspection to many In-Vitro Diagnostics Test Methods, Standards, Specifications, Laws and Regulations including:
Laboratories that perform In-Vitro Diagnostics testing and research may need to have certain local, domestic and international In-Vitro Diagnostics laboratory accreditations, licenses or certifications such as ISO 17025, A2LA, FDA GMP, EPA GLP, UKAS, etc.
In addition to In-Vitro Diagnostics testing and research, Contract Laboratory can assist with In-Vitro Diagnostics lab expertise, knowledge and support services such as: Technical Consulting, Method Development, Method Validation, Litigation Support, Patent Evaluation, Expert Testimony, Sustainability, Regulatory Support, Compliance, Government Filings, Prototyping, Troubleshooting, Process Development, Product Comparison, Competitor Analysis, Benchmarking, Audits, etc.
Contract Laboratory can help your company with the outsourcing of In-Vitro Diagnostics test laboratories in many areas and countries such as California, New York, USA, Canada, Mexico, South America, UK, Ireland, France, Germany, European Union, Russia, China, Hong Kong, Asia, Australia, Japan, Africa and the Middle East.
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