{"id":1440,"date":"2026-06-16T14:20:52","date_gmt":"2026-06-16T14:20:52","guid":{"rendered":"https:\/\/rcm1.rcm.upr.edu\/researchpahrmacy\/?page_id=1440"},"modified":"2026-06-30T12:53:46","modified_gmt":"2026-06-30T12:53:46","slug":"services","status":"publish","type":"page","link":"https:\/\/rcm1.rcm.upr.edu\/researchpharmacy\/services\/","title":{"rendered":"Services"},"content":{"rendered":"

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SERVICES PROVIDED BY THE MEDICAL SCIENCES CAMPUS PHARMACY:<\/h2><\/div><\/div>[vc_empty_space][vc_empty_space][\/vc_column][vc_column width=”1\/5″][vc_btn title=”Download Brochure” color=”black” size=”sm” align=”left” css=”” link=”url:https%3A%2F%2Frcm1.rcm.upr.edu%2Fresearchpharmacy%2Fwp-content%2Fuploads%2Fsites%2F37%2F2026%2F06%2Fservices.pdf”][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Start Up Fee (Including Pre Site Evaluation and Site Initiation visit), $3,000<\/strong><\/p>\n
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  • Pre site evaluation: Evaluating and preparing facilities for a potential clinical trial site.<\/li>\n
  • Site Initiation visit: Training study staff on the protocol, reviewing all necessary documentation and equipment, conducting a site tour, and discussing procedures for patient recruitment, data collection, and safety reporting to ensure the site is prepared for the clinical trial.<\/li>\n
  • Start Up: Materials\/supplies (binders, paper, labels, printing, thermometers) required to conduct the study; staff Training, IP storage area, source document preparation, security.<\/li>\n<\/ul>\n

    [\/vc_column_text][vc_single_image image=”1461″ img_size=”full” alignment=”center” css=””][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Accountability + Dispensation, $150* per study participant study visit<\/strong><\/p>\n

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    • Receipt, storage, review, IP dispensation, registry\/reports, etc.
      \n* could change base on study complexity.<\/li>\n<\/ul>\n

      [\/vc_column_text][vc_single_image image=”1463″ img_size=”full” alignment=”center” css=””][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Monitoring visits, $300 per occurrence<\/strong><\/p>\n

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      • Activities focus on the investigational product (IP), including checking inventory, verifying dispensing records, proper storage, and handling. All pharmacy-related documents are reviewed. Confirm that the site is following the protocol, discrepancies (if any) are discussed and clarified to ensure safety and data integrity. Support the monitor in preparing IP returns and coordinating pick up. (4\u20136 hrs).<\/li>\n<\/ul>\n

        [\/vc_column_text][vc_single_image image=”1462″ img_size=”full” alignment=”center” css=””][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Staff Trainings (specifically required by studies), $70 hr\/staff<\/strong><\/p>\n

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        • Attendance to compulsory trainings on protocol revisions<\/li>\n<\/ul>\n

          [\/vc_column_text][vc_single_image image=”1464″ img_size=”full” alignment=”center” css=””][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Closeout Visit, $1,000<\/strong><\/p>\n

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          • Complete investigational product (IP) accountability, ensuring unused IP is accounted for return or destruction, verifying and reconciling all drug logs, confirming all storage conditions and temperature logs are compliant. All drug-related documents are complete and properly archived. (4\u20136 hrs).<\/li>\n<\/ul>\n

            [\/vc_column_text][vc_single_image image=”1465″ img_size=”full” alignment=”center” css=””][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"

            [vc_row][vc_column width=”4\/5″][vc_empty_space][vc_empty_space][\/vc_column][vc_column width=”1\/5″][vc_btn title=”Download Brochure” color=”black” size=”sm” align=”left” css=”” link=”url:https%3A%2F%2Frcm1.rcm.upr.edu%2Fresearchpharmacy%2Fwp-content%2Fuploads%2Fsites%2F37%2F2026%2F06%2Fservices.pdf”][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]Start Up Fee (Including Pre Site Evaluation and Site Initiation visit), $3,000 Pre site evaluation: Evaluating and preparing facilities for a potential clinical trial site. Site Initiation visit: Training study staff on the protocol, reviewing all necessary documentation and equipment, conducting a site tour, and…<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-1440","page","type-page","status-publish","hentry","description-off"],"aioseo_notices":[],"aioseo_head":"\n\t\t\n\t\n\t\n\t\n\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t\n\t\t