Common use of Conduct of the Study Clause in Contracts

Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. radiology, pathology, cardiology and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for Xxxxxxxx, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

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Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. , radiology, pathology, cardiology and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for Xxxxxxxx, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

Conduct of the Study. (a) Institution and/or Investigator shall ensure declare that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. , radiology, pathology, cardiology and other nursing medical staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for XxxxxxxxCovance, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 1 contract

Samples: Clinical Trial Agreement

Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. radiology, pathology, cardiology medical and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Research Staff will document and report Study activities in an accurate, timely and complete manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for XxxxxxxxChiltern, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 1 contract

Samples: Clinical Trial Agreement

Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. , radiology, pathology, cardiology and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for XxxxxxxxChiltern, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. , radiology, pathology, cardiology and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for Xxxxxxxx, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 1 contract

Samples: Clinical Trial Agreement

Conduct of the Study. (a) Institution and/or Investigator shall ensure that all persons who have involvement in the Study and who are employees, independent contractors or agents of Institution and/or Investigator, including but not limited to pharmacy, laboratory. radiology, pathology, cardiology pharmacy and nursing staff (hereinafter „Research Staff”) have the knowledge and experience to undertake the Study and shall accurately, efficiently and expeditiously perform the Study in a professional and competent manner. Research Staff will document and report Study activities in an accurate, timely and complete manner. Wherever, in this Agreement, reference is made to obligations which are incumbent on the Institution and/or Investigator for services which may be performed by Research Staff, such reference is intended to include Research Staff. (b) By agreeing to the terms and conditions of this Agreement and performing the services for Xxxxxxxx, Institution and Investigator each represent and warrant that it/he/she is not in violation of any terms and conditions of any agreement for services or employment with any other individual or entity.

Appears in 1 contract

Samples: Clinical Trial Agreement

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