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Innovations in oncology have sparked advancements in the clinical trial industry and empowered COVID-19 research. Read more:

Gain a better understanding of clinical trial budget negotiations to reduce delays and study startup times.

Learn tips for developing and negotiating a clinical trial budget according to Medicare’s rules and regulations for device and drug clinical trials.

What are some of the key issues IRBs face when reviewing research that includes virtual trial technology? Read more:

CEO Gadi Saarony and Deb Tatton, Parexel Senior VP of Global Clinical Operations, discuss site and patient engagement. Read more:

CEO Gadi Saarony and Deb Tatton, Parexel Senior VP of Global Clinical Operations, discuss the evolving role of technology in research. Read more:

COVID-19 is rapidly changing the way research is conducted, namely how to conduct effective participant safety monitoring at a distance. Read more:

Audits to support your vendor qualification and management program should be conducted using a risk-based approach. Read more:

Combating the opioid crisis requires urgent, evidence-based approaches that address clinical, research, and education issues. Read more:

When do current Good Manufacturing Practices (cGMP) regulations apply? Read more for FDA expectations for the application of cGMP to investigational drugs:

Ensure your ISF is complete and avoid findings with these examples of specifically what auditors/inspectors look for during an audit. Read more:

Advarra is excited to introduce Fireside Chats, a series of virtual conversations. Fireside Chat is an informal conversation between an Advarra representative, and a clinical research thought leader.