How To Speed Up MLR Reviews: A Master Class By J&J, UCB, ex-Takeda Heads

A panel of experts from J&J, UCB and Takeda deliberated on the use of AI and internal processes to strike the right balance between speed and accuracy in MLR reviews that could protect a company from serious repercussions

Speakers from J&J, UCB And Takeda On The MLR Review Panel At Indegene Digital Summit 2024
Speakers On The MLR Review Panel At Indegene Digital Summit 2024 (Indegene)

Be quick or be safe? That’s a dilemma the pharmaceutical industry faces often as it seeks to bring a new drug to any market.

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Generative AI In Drug Discovery And India’s Potential To Leapfrog

 
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Heads of Novartis Biomedical, World Economic Forum and Indian majors like Sun Pharma’s SPARC, among others, discuss generative AI in drug discovery along with pointers for India to leapfrog the R&D process

With Fabhalta’s C3G Approval, Now Novartis Has To Find The Patients

 

Novartis US president Victor Bultó talked to Scrip about the company’s efforts to reach patients with rare kidney diseases who are candidates for Fabhalta.

Amgen’s Research VP On Goldilocks Viscosity, AI’s Hinge Moment

 
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Amgen’s AI model to predict proteins in the “bright Goldilocks zone of viscosity” with over 80% accuracy minus a wet lab experiment holds immense potential, VP Research Haldar said at an event as he spoke about a “hinge moment” for AI in pharma

MSD’s CIDO Williams: ‘We Must Shorten Technology Adoption Cycles’

 

MSD's chief information & digital officer emphasizes the need for pharma to accelerate technology adoption cycles to ensure drugs reach patients faster. The role of a robust digital backbone for seamless data flow, leadership commitment in digital transformation and an upcoming technology center in Hyderabad are other aspects he discussed.

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Merck Doubles Down On Oral Lipid-Lowering Drugs With Hengrui’s Lp(a) Asset

 
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Merck & Co., which already has an oral PCSK9 inhibitor in Phase III, licensed Hengrui’s Lipoprotein(a)-lowering small molecule HRS-5346 outside of Greater China for $200m up front.

Sanofi Nabs Priority Review For MS Drug Tolebrutinib

 
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A decision from the FDA is due by 28 September.

Stock Watch: Are Gene Therapy Prices Too High For Success?

 
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The promise of innovative therapies seems to have been constrained not by efficacy or safety concerns, but because the high price of treatments is incongruous with the reimbursement of short-course therapies.