For companies in the diagnostics and pharmaceutical fields, the time and cost involved in overcoming regulatory hurdles can greatly delay or even end the chance to get important innovations into practice. Through CLSI membership, your organization has the opportunity to collaborate with regulators, peers and customers on developing and implementing standards that are widely recognized to facilitate regulatory review for IVD devices, tests and other diagnostic products.
You’ll be subscribed to eCLIPSE™ Ultimate Access, our easy online portal featuring:
Your entire organization can find the most up-to-date technical standards they need—anytime, anywhere.
For questions or additional information, please contact CLSI’s Membership department at email@example.com.
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