Common use of Participating Staff Clause in Contracts

Participating Staff. Biogen shall appoint the Investigator as the medical specialist responsible for the conduct of the Trial on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and has the required experience, skills, knowledge and facilities for conducting the Trial. The Institution shall guarantee that the Trial will be duly performed by the Investigator in accordance with this Agreement. The Institution shall not be able to replace the Investigator with another investigator without the prior written consent of Biogen. The Investigator shall provide Biogen and its representatives with information regarding the other staff participating in the Trial (the Investigator and the other staff collectively referred to as the “Staff”). For the avoidance of doubt, the Staff shall throughout the term of this Agreement be under the supervision and control of the Institution. The Institution acknowledges and agrees that the Investigator enters into a separate agreement with Biogen and the CRO under which he/she will receive direct payment from the CRO for the services performed by the Investigator in connection with the Trial and by the other Staff members. The Institution assures that the performance of this separate agreement between Biogen and the Investigator will not constitute a violation of the Investigator’s duties nor a violation of the other Staff members’ duties. Agreements shall be concluded between Biogen and each respective Staff member, including but not limited to the Investigator, which shall stipulate terms and conditions of remuneration for each Staff member. Members of the Staff shall be solely responsible for due taxation of their income. Zdravotnické zařízení pověří příslušně kvalifikovaného zaměstnance a člena Personálu v pozici farmaceuta k zajištění řádného zacházení a následného výdeje Produktu dle požadavků Zkoušejícího, v souladu se Správnou lékárenskou praxí (vyhláška č. 84/2008 Sb.), Platnými zákony The Institution will authorize an employee and member of the Staff appropriately qualified to act as the pharmacist to secure proper handling and subsequent distribution of the Product as requested by the Investigator, and in accordance with Good Pharmacy Practice (Regulation No. 84/2008 Coll.), Applicable Laws and Regulations and the provisions a předpisy a ustanoveními Protokolu. of the Protocol.

Participating Staff. Biogen The Institution shall appoint the Investigator as the medical specialist responsible for the conduct of the Trial on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and has the required experience, skills, knowledge experience and facilities means for conducting the Trial. The Institution shall guarantee that the Trial will be duly performed by the Investigator in accordance with this Agreement. The Institution shall not be able to replace the Investigator with another investigator without the prior written consent of Biogen. The Institution shall provide, and shall cause the Investigator shall provide to provide, Biogen and its representatives with information regarding the other staff participating in the Trial (the Investigator and the other staff collectively referred to as the “Staff”). For the avoidance of doubt, the Staff shall throughout the term of this Agreement be under the supervision and control of the Institution, and the Institution shall without limitation be responsible for ensuring that the Staff act in accordance with the Applicable Laws and Regulations and, Biogen’s and its representatives’ reasonable instructions. The Institution acknowledges and agrees that the Investigator enters into a separate agreement with Biogen and the CRO under which he/she will receive direct payment from the CRO for the services performed by the Investigator in connection with the Trial and by the other Staff members. The Investigator shall be responsible for the compensation of any Staff members that he/she decides to use in connection with the conduct of the Trial. The Institution assures that the performance of this separate agreement between Biogen and the Investigator will not constitute a violation of the Investigator’s duties nor a violation of the other Staff members’ duties. Agreements shall be concluded between Biogen and each respective Staff member, including but not limited to the Investigator, which shall stipulate terms and conditions of remuneration for each Staff member. Members of the Staff shall be solely responsible for due taxation of their income. Zdravotnické zařízení pověří příslušně kvalifikovaného zaměstnance a člena Personálu v pozici farmaceuta k zajištění řádného zacházení a následného výdeje Produktu dle požadavků Zkoušejícího, v souladu se Správnou lékárenskou praxí (vyhláška č. 84/2008 Sb.), Platnými zákony a předpisy a ustanoveními Protokolu. The Institution will authorize an employee and member of the Staff appropriately qualified to act as the pharmacist to secure proper handling and subsequent distribution of the Product as requested by the Investigator, and in accordance with Good Pharmacy Practice (Regulation No. 84/2008 Coll.), Applicable Laws and Regulations and the provisions a předpisy a ustanoveními Protokolu. of the Protocol.