Everest Group
JUNE 16, 2023
Despite challenges and regulations, the life sciences industry is actively exploring GAI’s possibilities. Although GAI can potentially disrupt the life sciences technology ecosystem in many significant ways, navigating the various risks and challenges that come with its implementation in this highly regulated industry will be critical.
Perficient Digital Transformation
OCTOBER 18, 2021
The results of these analyses help pharmaceutical companies better understand the impact drugs can have on the human body and influences critical decisions in the drug manufacturing process. Non-compartmental analysis (NCA) is an essential activity within the drug development process.
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Perficient Digital Transformation
JULY 24, 2023
How are you making a difference for our clients, colleagues, and communities? As a lead business consultant in the computer system validation department, I plan, write, implement, and review the computer systems validation plan and protocols within highly regulated industries. Thanks for joining me today, Kaushal.
Perficient Digital Transformation
JANUARY 16, 2024
Healthcare and life sciences are two of the largest industry verticals Perficient serves, with a substantial roster of clients spanning providers, plans, pharmaceutical, biotech, and medical device companies. Kevin: Healthcare and life sciences are highly regulated industries that face higher consumer and governmental scrutiny.
Perficient Digital Transformation
JUNE 1, 2022
We also discussed the things she values about Perficient’s culture of collaboration and inclusion. As the head of the computer systems validation department, I plan, write, implement, and review the computer systems validation protocols within highly regulated industries. READ MORE: Collaboration at Perficient .
Everest Group
JUNE 7, 2023
However, given the strict industry regulations, human intervention/oversight remains essential for the overall usage of GAI. Exhibit 1 illustrates the key use cases that enterprises are striving to unlock in the near term.
Transperfect
SEPTEMBER 16, 2021
The TMF is a source of evidence examined by regulators to ensure credible clinical trial data and protection of patients’ rights and safety. Their scalability allows them to work globally with small biotechnology or large pharmaceutical companies, depending on an organization’s needs. Why You Need Them.
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