Common use of Study Registration by Pfizer Clause in Contracts

Study Registration by Pfizer. Pfizer commits to register, on the National Institutes of Health Clinical Trials Data Bank (xxx.xxxxxxxxxxxxxx.xxx), all Pfizer- sponsored Phase 1 through 4 interventional and non-interventional studies that involve the use of a Pfizer product and evaluate the safety or efficacy of that product. Pfizer will also register Pfizer-sponsored studies on other listings of ongoing studies maintained by competent regulatory authorities where there is a regulatory requirement to do so.

Study Registration by Pfizer. Pfizer commits to register, on the National Institutes of Health Clinical Trials Data Bank (xxx.xxxxxxxxxxxxxx.xxx)) , all Pfizer- sponsored Phase 1 through 4 interventional and non-interventional studies that involve the use of a Pfizer product Product and/or Pfizer Drug and evaluate the safety or efficacy of that product. Pfizer will also register Pfizer-sponsored studies on other listings of ongoing studies maintained by competent regulatory authorities where there is a regulatory requirement to do so.

Study Registration by Pfizer. Pfizer commits to register, on the National Institutes of Health Clinical Trials Data Bank (xxx.xxxxxxxxxxxxxx.xxx), all Pfizer- Pfizer-sponsored Phase 1 through 4 interventional and non-interventional studies that involve the use of a Pfizer product and evaluate the safety or efficacy of that product. Pfizer will also register Pfizer-Pfizer- sponsored studies on other listings of ongoing studies maintained by competent regulatory authorities where there is a regulatory requirement to do so.

Study Registration by Pfizer. Pfizer commits to register, on the National Institutes of Health Clinical Trials Data Bank (xxx.xxxxxxxxxxxxxx.xxx), all Pfizer- Pfizer-sponsored Phase 1 through 4 interventional and non-non- interventional studies that involve the use of a Pfizer product and evaluate the safety or efficacy of that product. Pfizer will also register Pfizer-sponsored studies on other listings of ongoing studies maintained by competent regulatory authorities where there is a regulatory requirement to do so. 16.