Random Musings From The Clinical Trials Guru
Business:Entrepreneurship
FDA Clinical Research DCT Guidance 2023: Clinical Research Site Owner Reacts! Ep.715
2023-06-23
Veeva Site Vault: https://sites.veeva.com/
Versatrial: http://www.versatrial.io
CRIO: http://www.clinicalresearch.io
Inato: https://go.inato.com/3VnSro6
Join me at my conference! http://www.saveoursites.com
Text Me: (949) 415-6256
My podcast is Random Musings From The Clinical Trials Guru
Listen on Spotify: https://open.spotify.com/show/7JF6FNvoLnBpfIrLNCcg7a
GET THE BOOK! https://www.amazon.com/dp/1090349521/...
Text "guru" to 855-942-5288 to join VIP list!
My blog: http://www.TheClinicalTrialsGuru.com
My CRO and Site Network: http://www.DSCScro.com
My CRA Academy: http://www.TheCRAacademy.com
My CRC Academy: http://www.TheCRCacademy.com
Latinos In Clinical Research: http://www.LatinosinClinicalResearch.com
The University Of Clinical Research: https://www.theuniversityofclinicalresearch.com/
My TikTok: DanSfera
LifeBoost Coffee: https://lifeboostcoffee.com/products/biotics-brew?_pos=2&_sid=576df78bc&_ss=r&nb_platform=shareasale
Timestamps:
Intro. (0:00)
Strategies to bring the trial to the patient. (3:23)
How remote assessments differ from on-site assessments. (8:30)
Why didn’t virtual trials work? (13:57)
Trial related services should not differ from clinical practice. (18:28)
Sponsor role and responsibility. (23:15)
The investigators role and responsibilities. (27:42)
Documentation investigators sub investigators. (33:42)
More liability, more liability and less control. (38:33)
Safety monitoring plan for patients. (43:39)
More Episodes
Get this podcast on your
phone, FREE
