DIA Exhibitor Gallery. You are invited to visit the following company booths at DIA.
You are invited to visit these DIA 2012 booths:
Booth No. 1539Catalentwww.calatent.com
Phone: +1 888 SOLUTION (7658846)
E-mail:solutions@catalent.com
Booth No. 1733Cromsourcewww.cromsource.com
Phone: +39 045 8222811
E-mail:cromsource@cromsource.com
Booth No. 2725ERTwww.ert.com
Contact: Tom Avery
Phone: 215-972-0420
E-mail: eresearch@ert.com
Booth No. 1951Forte Research Systemswww.forteresearch.com
Contact: Brian Wulff
Phone: 608-826-6000
E-mail: Allegro@ForteResearch.com
Booth No. 1148Globalcare Clinical Trialswww.globalcarect.com
Phone: 847-282-3280
E-mail: info@globalcarect.com
Booth No. 2112LabCorpwww.labcorp.com/clinicaltrials
Contat: Shailesh Maingi
Phone: 877-788-8861
E-mail: clintrialssales@labcorp.com
Booth No. 2441REGISTRAT-MAPIwww.registratmapi.com
Phone: 800-381-7878
E-mail: info@registratmapi.com
Booth No. 2533Spectra Clinical Research www.spectraclinicalresearch.com
Phone: 800-517-7157
E-mail: sales.spectraclinicalresearch@fmc-na.com
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Regulatory Compliance With eCOAs
April 26th 2024In the fourth and final part of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA discusses how the regulatory stance on electronic clinical outcome assessments has changed over the years and what it could look like in the future.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.