Advarra (@advarra) 's Twitter Profile
Advarra

@advarra

Advancing clinical research by enabling the research ecosystem to develop life-changing therapies.

Reviews | Consulting | Technology | Professional Services

ID: 1954787316

linkhttp://www.advarra.com calendar_today11-10-2013 18:42:35

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We are excited to partner with Blackstone and Canada Pension Plan Investment Board as we work to make clinical research safer, smarter and faster. bit.ly/3tumCgx

We are excited to partner with Blackstone and Canada Pension Plan Investment Board as we work to make clinical research safer, smarter and faster. bit.ly/3tumCgx
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#Clinicalresearch professionals routinely interact with IRB and IBC, but what other committees are reviewing research? James Riddle will delve into the role and function of DMCs and EACs in ACRP - Assoc. of Clinical Research Profession's upcoming #webinar! Register now: bit.ly/3MWjxwB

#Clinicalresearch professionals routinely interact with IRB and IBC, but what other committees are reviewing research? <a href="/JR_KinetiqIdeas/">James Riddle</a> will delve into the role and function of DMCs and EACs in <a href="/ACRPDC/">ACRP - Assoc. of Clinical Research Profession</a>'s  upcoming #webinar! Register now: bit.ly/3MWjxwB
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Advarra is attending CAR & T Cell Therapie’s conference on “Improving the Safety and Efficacy of Your Novel CAR Modalities Through Translational Science and Cutting Edge Clinical Data”. We are excited to discuss innovations in CAR-T Therapy: bit.ly/3zGLwxw

Advarra is attending CAR &amp; T Cell Therapie’s conference on “Improving the Safety and Efficacy of Your Novel CAR Modalities Through Translational Science and Cutting Edge Clinical Data”. We are excited to discuss innovations in CAR-T Therapy: bit.ly/3zGLwxw
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Are you attending #DIA2022? Advarra’s Sharon Ayd will present on the differences in CMC regulatory requirements globally and its impact on access to medicines: bit.ly/3xWuCJT #DIA2022

Are you attending #DIA2022? Advarra’s Sharon Ayd will present on the differences in CMC regulatory requirements globally and its impact on access to medicines: bit.ly/3xWuCJT #DIA2022
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Are you attending #DIA2022? Advarra’s Sharon Ayd will present on the differences in CMC regulatory requirements globally and its impact on access to medicines: bit.ly/3xWuCJT #DIA2022

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In this blog, learn how we introduced the capability to store and manage additional key study documents; subject binders and standard operating procedures (SOPs). bit.ly/3bgMHK0 #AdvarraeReg

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Join us for a two-part webinar series where in Part One, Advarra experts JV Rao and Wendy Tate examine the current state of #siteidentification and identify areas of risk mitigation and optimization opportunities. Register now: bit.ly/3N4Jx99

Join us for a two-part webinar series where in Part One, Advarra experts JV Rao and Wendy Tate examine the current state of #siteidentification and identify areas of risk mitigation and optimization opportunities. Register now:  bit.ly/3N4Jx99
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Establishing a compliant pharmacovigilance (PV) function from scratch is often an overwhelming exercise. Our blog outlines four critical questions to ask when supporting emerging biotech organizations as they establish a successful PV organization. bit.ly/3y8y4kP

Establishing a compliant pharmacovigilance (PV) function from scratch is often an overwhelming exercise. Our blog outlines four critical questions to ask when supporting emerging biotech organizations as they establish a successful PV organization. bit.ly/3y8y4kP
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In this podcast episode, Advarra’s Robann Cunningham and the Patient Empowerment Network’s Robin Barnes discusses patient empowerment and advocacy. Listen here: bit.ly/3n3ubY6

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Institutional sites are critical to successful clinical research and the advancement of healthcare. That’s why at Advarra, everything we do is driven by site centricity. In this blog, learn how Advarra plays a role in the movement toward site centricity. bit.ly/3pwarhA

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Regulatory agency guidance in the U.S. and EU strongly recommends keeping DSMBs completely independent from parties sponsoring, organizing, or conducting the clinical trial. Get the truth on what a DSMB does and how to set one up in this free white paper. bit.ly/3Opy3y5

Regulatory agency guidance in the U.S. and EU strongly recommends keeping DSMBs completely independent from parties sponsoring, organizing, or conducting the clinical trial. Get the truth on what a DSMB does and how to set one up in this free white paper. bit.ly/3Opy3y5
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Join Luke Gelinas and Reid Blackman Ph.D. on our latest podcast as they discuss artificial intelligence in clinical research. From discriminatory AI to the IRB review process, Luke and Reid dive into the exciting world of #AIEthics. bit.ly/39Wny6U

Join Luke Gelinas and Reid Blackman Ph.D. on our latest podcast as they discuss artificial intelligence in clinical research. From discriminatory AI to the IRB review process, Luke and Reid dive into the exciting world of #AIEthics.  bit.ly/39Wny6U
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Advarra is proud to sponsor NWABR's hybrid IRB conference "Back to Basics." Our own Julie Ozier will be opening the conference. We hope to see you there! Register today: nwabr.org/IRB

Advarra is proud to sponsor <a href="/nwabr/">NWABR</a>'s hybrid IRB conference "Back to Basics." Our own Julie Ozier will be opening the conference. We hope to see you there! Register today: nwabr.org/IRB
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Curious about how #AI is used in clinical research? Want to learn more about discriminatory AI? Check out this podcast where IRB Chairperson Luke Gelinas and AI Ethics Advisor Reid Blackman discuss #AIethics & the implications for #clinicalresearch. bit.ly/3yC46pL

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Research into participant experiences has consistently shown their desire to learn the results of research to which they’ve contributed. bit.ly/3NM9XwK

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Understanding the factors that influence the decision to participate in a study helps research professionals diagnose enrollment problems. advarra.com/resource-libra…

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Attending Cell & Gene Meeting on the Mesa? Let's chat! Advarra representatives will be onsite to learn about your challenges - and successes - in the cell and gene research space. We look forward to seeing you!

Attending Cell &amp; Gene Meeting on the Mesa? Let's chat! Advarra representatives will be onsite to learn about your challenges - and successes - in the cell and gene research space. We look forward to seeing you!
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Ethical oversight committees continue to innovate to keep pace with the rapid changes and evolution of research conduct. advarra.com/blog/unpacking…

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An investigator-initiated trial (IIT) occurs when an investigator creates the idea for a study, develops the protocol, and serves as the sponsor and investigator for the trial. Download our latest eBook: bit.ly/3WRGeIJ

An investigator-initiated trial (IIT) occurs when an investigator creates the idea for a study, develops the protocol, and serves as the sponsor and investigator for the trial. 

Download our latest eBook: bit.ly/3WRGeIJ
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We're dedicated to serving the clinical research community at Advarra, and that means staying on top of the latest trends. Our new eBook, "2023 Trends Impacting Clinical Research," can help you stay informed and adapt to the changes. #ClinicalResearch bit.ly/40132XZ

We're dedicated to serving the clinical research community at Advarra, and that means staying on top of the latest trends. Our new eBook, "2023 Trends Impacting Clinical Research," can help you stay informed and adapt to the changes. 

#ClinicalResearch bit.ly/40132XZ