Common use of Participating Staff Clause in Contracts

Participating Staff. The Institution shall choose the Investigator on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and has the required experience and means for conducting the Trial. The Institution shall guarantee that this Agreement will be duly performed by the Investigator chosen on its responsibility. 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 to provide, Biogen and its representatives with information regarding the staff participating in the Trial (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 Investigator, and the Institution and Investigator 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. 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 of the Protocol.

Participating Staff. The Institution shall choose the and Investigator on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and he has the required experience and means for conducting the Trial. The Institution shall guarantee Trial and that he will duly perform the subject matter of this Agreement will be duly performed by the Investigator chosen on its responsibilityAgreement. The Institution shall not be able to replace the Investigator with another Investigator without the prior written consent of Biogen. The Institution and Investigator shall provide, and shall cause the Investigator to provide, provide Biogen and its representatives with information regarding the staff participating in the Trial (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 Investigator, and the Institution and Investigator 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. 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 of the Protocol.

Participating Staff. The Institution shall choose the Investigator on its own responsibility. The Institution hereby declares that the Investigator he/she has undergone the necessary training and has the required experience and means for conducting the Trial. The Institution acknowledges that Investigator shall guarantee that this Agreement will be duly performed by the Investigator chosen on its responsibilityduly. 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 to provide, Biogen and its representatives with information regarding the staff participating in the Trial (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 Investigator, and the Institution and Investigator 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. 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 of the Protocol.

Participating Staff. The Institution shall choose the and Investigator on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and he has the required experience and means for conducting the Trial. The Institution shall guarantee Trial and that he will duly perform the subject matter of this Agreement will be duly performed by the Investigator chosen on its responsibilityAgreement. 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 to provide, shall provide Biogen and its representatives with information regarding the staff participating in the Trial (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 Investigator, and the Institution and Investigator 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. 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 of the Protocol.

Participating Staff. The Institution shall choose the Investigator on its own responsibility. The Institution hereby declares that the Investigator has undergone the necessary training and he/she has the required experience and means for conducting the Trial. The Institution and Investigator shall guarantee that duly perform the conditions of this Agreement will be duly performed by the Investigator chosen on its responsibilityAgreement. 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 to provide, Biogen and its representatives with information regarding the staff participating in the Trial (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 Investigator, and the Institution and Investigator shall without limitation be responsible for ensuring that the Staff act in accordance with the Applicable Laws and Regulations Regulations, guidelines issued by the State Institute for Drug Control – LEK-12 and, Biogen’s and its representatives’ reasonable instructions. 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 of the Protocol.