Common use of Biological Samples Clause in Contracts

Biological Samples. If so specified in the Protocol and the informed consent document, Principal Investigator may collect and provide to CRO, Sponsor or their designee, biological samples obtained from trial subjects (e.g., blood, urine, tissue, saliva, etc) for testing that is not directly related to trial subject care or safety monitoring, such as pharmacokinetic, pharmacogenomic, or biomarker testing (“Biological Samples”). Biological Samples may include Personal Data (as defined elsewhere herein) of trial subjects of which the processing is governed by the applicable legislation in the territory of the Slovak Republic. For the avoidance of doubt, the Contracting Parties explicitly confirm, that the restriction of processing Personal Data of trial subjects exclusively in pseudonymized form, as indicated in Appendix 2, Art. 10.5, shall apply in full extent also to Biological Samples of trial subjects. a.

Biological Samples. If so specified in the Protocol and the informed consent document, Principal Investigator may collect and provide to CRO, Sponsor or their designee, biological samples obtained from trial subjects (e.g., blood, urine, tissue, saliva, etc) for testing that is not directly related to trial subject care or safety monitoring, such as pharmacokinetic, pharmacogenomic, or biomarker testing (“Biological Samples”). Biological Samples may include Personal Data (as defined elsewhere herein) of trial subjects of which the processing is governed by the applicable legislation in the territory of the Slovak Republic. For the avoidance of doubt, the Contracting Parties explicitly confirm, that the restriction of processing Personal Data of trial subjects exclusively in pseudonymized form, as indicated in Appendix 2, Art. 10.5, shall apply in full extent also to Biological Samples of trial subjects. a..