CAMBRIDGE, Mass.--(BUSINESS WIRE)--InVivo Therapeutics Holdings Corp. (NVIV) today announced that it has sent to the United States Food and Drug Administration the revised protocol and related study documents for a clinical study to test the safety of its investigational scaffold device for spinal cord repair. The revised protocol includes all changes that were conditions of approval by the FDA. On Monday, it will send the revised protocol and related study documents to six sites in the United States so that they can now begin their Institutional Review Board submissions and finalize clinical study contracts with InVivo.
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