Personal Information of the Parties a. Both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Provider may be called upon to provide personal information to INC Research. For the Principal Investigator, this personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). For other employees/contractors of the Principal Investigator, this Personal Information may include names and contact information. The Personal Information may be stored electronically by INC Research and/or transferred to third parties (situated throughout the world) for the following purposes: (1) the conduct of clinical trials; (2) verification by government or regulatory agencies, the Sponsor, INC Research, and their agents and affiliates; (3) compliance with legal and regulatory requirements; (4) publication on xxx.xxxxxxxxxxxxxx.xxx and other websites and/or databases that serve a comparable purpose; (5) storage in databases to facilitate the 11.5. Platnost závazků po ukončení smlouvy Tyto závazky nepoužívat a nezvešejňovat důverné informace, s výjimkou údajů o klinickém hodnocení (definovaných níže) a údajů z analýz biologických vzorků (definovaných níže), zůstanou v platnosti sedm (7) let po ukončení této smlouvy. Povolené použití a zvešejnení údajů o klinickém hodnocení je popsáno v bode 15 (Publikace) této smlouvy. 11.6. Vrácení důverných informací Pokud o to zadavatel písemne požádá, poskytovatel a hlavní zkoušející na náklady zadavatele vrátí všechny důverné informace s výjimkou informací, které musí podle platných zákonů zůstat na pracovišti klinického hodnocení. Poskytovatel a hlavní zkoušející si však mohou ponechat jednu archivní kopii důverných informací výhradne za účelem stanovení rozsahu povinností v rámci této smlouvy. 11.7. Osobní údaje stran a. Hlavní zkoušející a zamestnanci/smluvní partneši poskytovatele mohou být pšed i behem klinického hodnocení vyzváni, aby společnosti INC Research poskytli osobní údaje. V pšípade hlavního zkoušejícího mohou tyto osobní údaje zahrnovat jména, kontaktní informace, pracovní zkušenosti, profesní kvalifikaci, publikace, životopisy, vzdelání a/nebo informace o platbách hrazených dle této smlouvy (dále jen “osobní údaje”). U ostatních zamestnanců/smluvních partnerů hlavního zkoušejícího mohou tyto osobní údaje zahrnovat jm...
Personal Information of the Parties a. Both prior to and during the course of the Trial, the Principal Investigator and the employees/contractors of the Institution may be called upon to provide personal information to INC Research. This personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). The Personal Information may be stored electronically by INC Research and/or transferred to third parties (situated throughout the world) for the following purposes: (1) the conduct of clinical trials; (2) verification by government or regulatory agencies, the Sponsor, INC Research, and their agents and affiliates; (3) compliance with legal and regulatory requirements; (4) publication on xxx.xxxxxxxxxxxxxx.xxx and other websites and/or databases that serve a comparable purpose; (5) storage in databases to facilitate the selection of investigators for future clinical trials; and (6) anti-corruption compliance. Institution confirms thatits employees/contractors consent to provide the Personal Information to INC Research to be electronically stored by INC Research and for INC Research to transfer to third parties as stated above. b. Institution shall process Personal Information relating to INC Research’s employees/contractors ktorí potrebujú poznať dôverné informácie za účelom výkonu skúšania a podliehajú povinnostiam zachovania dôvernosti, ktoré nie sú menej prísne ako tie, ktoré obsahuje táto zmluva. Inštitúcia oznámi pomocným skúšajúcim a výskumným pracovníkom dôvernú povahu dôverných informácií a zostane zodpovedná za akékoľvek porušenie zo strany pomocných skúšajúcich alebo výskumných pracovníkov. 9.8.
Personal Information of the Parties a. Both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Provider may be called upon to provide personal information to INC Research. For the Principal Investigator, this personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). For other employees/contractors of the Provider, this Personal Information may include names and contact information. The Personal Information may be stored electronically by INC Research and/or transferred to third parties (situated throughout the world) for the following purposes: (1) The conduct of clinical trials; (2) Verification by government or regulatory agencies, the Sponsor, INC Research and their agents and affiliates; (3) Compliance with legal and regulatory requirements; (4) Publication on xxx.xxxxxxxxxxxxxx.xxx and other websites and/or databases that serve a comparable purpose; (5) Storage in databases to facilitate the selection of investigators for future clinical trials; and (6) Anti-corruption compliance. Provider confirms that the Principal Investigator and employees/contractors of Provider consent to provide the Personal Information to INC Research to be electronically stored by INC Research and for INC Research to transfer to third parties as stated above. b. Provider shall process Personal Information relating to INC Research’s employees/contractors only to the extent, and in such a manner as is necessary for the purposes of this Agreement. Provider shall not transfer such Personal Information relating to INC Research’s employees/contractors to a third party without the prior written consent of INC Research. 12.2 Osobní údaje stran a. Hlavní zkoušející a zaměstnanci/smluvní partneši poskytovatele zdravotních služeb mohou být pšed i během klinického hodnocení vyzváni, aby společnosti INC Research poskytli osobní údaje. V pšípadě hlavního zkoušejícího mohou tyto osobní údaje zahrnovat jména, kontaktní informace, pracovní zkušenosti, profesní kvalifikaci, publikace, životopisy, vzdělání a/nebo informace o platbách hrazených dle této smlouvy (dále jen “osobní údaje”). U ostatních zaměstnanců/smluvních partnerů poskytovatele zdravotních služeb mohou tyto osobní údaje zahrnovat jména a kontaktní informace. Společnost INC Research může osobní údaje uchovávat v el...
Personal Information of the Parties a. Both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Institution may be called upon to provide personal information to INC Research. For the Principal Investigator, this personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). For other employees/contractors of the Principal Investigator, this Personal Information may include names and contact information. The Personal Information may be stored electronically by INC Research and/or transferred to third parties (situated throughout the world) for the following purposes: (1) the conduct of clinical trials; (2) verification by government or regulatory agencies, the Sponsor, INC Research, and their agents and affiliates; (3) compliance with legal and regulatory requirements; (4) publication on xxx.xxxxxxxxxxxxxx.xxx and other websites and/or databases that serve a comparable purpose; (5) storage in databases to facilitate the 11.5. Platnost závazků po ukončení smlouvy Tyto závazky nepoužívat a nezveřejňovat důvěrné informace, s výjimkou údajů o klinickém hodnocení (definovaných níže) a údajů z analýz biologických vzorků (definovaných níže), zůstanou v platnosti sedm (7) let po ukončení této smlouvy. Povolené použití a zveřejnění údajů o klinickém hodnocení je popsáno v bodě 15 (Publikace) této smlouvy. 11.6.
Personal Information of the Parties účelem stanovení rozsahu závazků vyplývajících z této smlouvy. 9.7. Osobní údaje stran
Personal Information of the Parties. 11.7.1 Both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Provider may be called upon to provide personal information to Syneos Health. For the Principal Investigator, this personal information may include names, contact information, country of licensure, license number, work experience and professional qualifications, publications, resumes, educational background and/or information relating to all payments and transfer of value made to Providerand/or Principal Investigator under this Agreement (“Personal Information”). Syneos Health may further disclose and/or publish such information publicly in accordance with applicable laws. For other employees/contractors of theProvider, this Personal Information may include names and contact information. The Personal Information may be stored electronically by Syneos Health and/or transferred to third parties (situated throughout the world) for the following purposes: 11.7.1.1 the conduct of clinical trials; 11.7.1.2 verification by government or regulatory agencies, the Sponsor, Syneos Health, and their agents and affiliates; 11.7.1.3 compliance with legal and regulatory requirements; 11.7.1.4 publication on xxx.xxxxxxxxxxxxxx.xxx and other websites and/or databases that serve a comparable purpose; 11.7.1.5 storage in databases to facilitate the v bodě 15 (Publikace) této smlouvy. 11.6.
Personal Information of the Parties a. Both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Institution may be called upon to provide personal information to INC Research. For the Principal Investigator, this personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). For other employees/contractors of the Institution, this Personal Information may include names and 12.1
Personal Information of the Parties a. Healthcare Provider acknowledges that both prior to and during the course of the Trial, the Principal Investigator and other employees/contractors of the Healthcare Provider may be called upon to provide personal information to INC Research. For the Principal Investigator, this personal information may include names, contact information, work experience and professional qualifications, publications, resumes, educational background and/or information relating to payments made pursuant to this Agreement (“Personal Information”). For other employees/contractors of the Healthcare Provider, this Personal Information may include names and contact information. The Personal Information may be stored electronically by INC Research and/or transferred to third parties (situated throughout the world) for the following purposes: (1) the conduct of clinical trials; (2) verification by government or regulatory agencies, the Sponsor, INC Research, and their agents and affiliates; (3) compliance with legal and regulatory requirements; (4) publication on xxx.xxxxxxxxxxxxxx.xxx, xxxx://xxx.xxxx.xx/modules/evaluation/and other websites and/or databases that serve a comparable purpose; (5) storage in databases to facilitate the selection of investigators for future clinical trials; and b.
Personal Information of the Parties
