dev: update collection link

Author: megasanjay

dev/datasetRecord.json

@@ -2029,7 +2029,7 @@
         {
           "id": 3,
           "question": "Are there any datasheets created for any versions of this dataset?",
-          "response": "There was a previous datasheet created for the first version of the dataset, which consisted of data collected during the pilot data collection phase. It is available here: https://docs.aireadi.org/docs/1/dataset/healthsheet.\n\nThere was also a previous datasheet created for the second version of the dataset, which consisted of data collected up to the end of the first full year of the study. It is available here: https://docs.aireadi.org/docs/2/dataset/healthsheet"
+          "response": "There was a previous datasheet created for the first version of the dataset, which consisted of data collected during the pilot data collection phase. It is available here: https://docs.aireadi.org/docs/1/dataset/healthsheet. \n\nThere was also a previous datasheet created for the second version of the dataset, which consisted of data collected up to the end of the first full year of the study. It is available here: https://docs.aireadi.org/docs/2/dataset/healthsheet"
         },
         {
           "id": 4,
@@ -2320,7 +2320,7 @@
         {
           "id": 9,
           "question": "Did the individuals in question consent to the collection and use of their data? If so, please describe (or show with screenshots or other information) how consent was requested and provided, and provide a link or other access point to, or otherwise reproduce, the exact language to which the individuals consented.",
-          "response": "Informed consent to participate was required before participation in any part of the protocol (including questionnaires). Potential participants were given the option to read all consent documentation electronically (e-consent) before their visit and give their consent with an electronic signature without verbal communication with a clinical research coordinator. Participants may access e-consent documentation in REDCap and decide at that point they do not want to participate or would like additional information. The approved consent form for the principal project site University of Washington is available [here](https://docs.aireadi.org/v3/AI-READI%20Consent_Form_Standard_v2.0_Mod2%2017May2023_useforpilot.pdf). The other clinical sites had IRB reliance and used the same consent form, with minor institution-specific language incorporated depending on individual institutional requirements."
+          "response": "Informed consent to participate was required before participation in any part of the protocol (including questionnaires). Potential participants were given the option to read all consent documentation electronically (e-consent) before their visit and give their consent with an electronic signature without verbal communication with a clinical research coordinator. Participants may access e-consent documentation in REDCap and decide at that point they do not want to participate or would like additional information. The approved consent form for the principal project site University of Washington is available [here](https://docs.aireadi.org/v3/AI-READI%20Consent_Form_Standard_Mod17May2023_useforpilot.pdf). The other clinical sites had IRB reliance and used the same consent form, with minor institution-specific language incorporated depending on individual institutional requirements."
         },
         {
           "id": 10,

dev/miniDatasetRecord.json

@@ -2271,7 +2271,7 @@
         {
           "id": 9,
           "question": "Did the individuals in question consent to the collection and use of their data? If so, please describe (or show with screenshots or other information) how consent was requested and provided, and provide a link or other access point to, or otherwise reproduce, the exact language to which the individuals consented.",
-          "response": "Informed consent to participate was required before participation in any part of the protocol (including questionnaires). Potential participants were given the option to read all consent documentation electronically (e-consent) before their visit and give their consent with an electronic signature without verbal communication with a clinical research coordinator. Participants may access e-consent documentation in REDCap and decide at that point they do not want to participate or would like additional information. The approved consent form for the principal project site University of Washington is available [here](https://docs.aireadi.org/v3/AI-READI%20Consent_Form_Standard_v2.0_Mod2%2017May2023_useforpilot.pdf). The other clinical sites had IRB reliance and used the same consent form, with minor institution-specific language incorporated depending on individual institutional requirements."
+          "response": "Informed consent to participate was required before participation in any part of the protocol (including questionnaires). Potential participants were given the option to read all consent documentation electronically (e-consent) before their visit and give their consent with an electronic signature without verbal communication with a clinical research coordinator. Participants may access e-consent documentation in REDCap and decide at that point they do not want to participate or would like additional information. The approved consent form for the principal project site University of Washington is available [here](https://docs.aireadi.org/v3/AI-READI%20Consent_Form_Standard_Mod17May2023_useforpilot.pdf). The other clinical sites had IRB reliance and used the same consent form, with minor institution-specific language incorporated depending on individual institutional requirements."
         },
         {
           "id": 10,