Dear colleagues,
 Certara is pleased to announce the release of pyDarwin, version 1.0. pyDarwin 
is a machine learning solution for NONMEM model selection. This is an open 
source package, released under GNU GENERAL PUBLIC LICENSE. The interface is 
general, any combination of options (compartments, between subject variability, 
residual variability, between occasion variability, covariates, different 
absorption models, different pharmacodynamic models, different number of ODEs, 
nonlinear processes etc) can be searched for the optimal combination. In 
addition, user defined R or python code can be run after each NONMEM model 
allowing user defined penalties, such as PPC to be included in the search 
criteria. pyDarwin is an all python solution, supported on Windows, Linux and 
Sun Grid engine. The source package can be downloaded from
https://github.com/certara/pyDarwin
and the documentation can be found here:
https://certara.github.io/pyDarwin/html/index.html<https://nam11.safelinks.protection.outlook.com/?url=https%3A%2F%2Fcertara.github.io%2FpyDarwin%2Fhtml%2Findex.html&data=05%7C01%7Cmark.sale%40certara.com%7C31a3289a45dc487bd7cc08da7637b77b%7C7287abd30220456e98514352bae208c9%7C1%7C0%7C637952278937389398%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=Ex3%2BetN5WUFPhlmGouAB5SojE4WlEUGXJJFcc49sDM0%3D&reserved=0>

Feel free to contact me with any questions.

Mark

This work was supported by FDA/NIH grant (U01FD007355) (Development of a model 
selection method for population pharmacokinetics analysis by deep-learning 
based reinforcement learning (RFA-FD-21-027)). Views expressed in this 
announcement do not represent FDA's views or policy.
Rob Bies lab at the University at Buffalo is a collaborator on this work and a 
co-investigator for this work.  His laboratory has contributed sample datasets 
and suggestions on the strategies for model search



Mark Sale M.D.
Vice President
Integrated Drug Development
mark.s...@certara.com
Remote-Forestville CA
Office Hours 9 AM - 5 PM Eastern Time
+1 302-516-1684
www.certara.com
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From: owner-nmus...@globomaxnm.com <owner-nmus...@globomaxnm.com> On Behalf Of 
Rebecca Baillie
Sent: Wednesday, August 10, 2022 10:14 AM
To: nmusers@globomaxnm.com
Subject: [NMusers] Webinar: Injecting Reality into The Commercial Due Diligence 
Process for In-Licensing, Partnering, or Purchasing Pharmaceutical Assets in 
Development.

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Injecting Reality into The Commercial Due Diligence Process for In-Licensing, 
Partnering, or Purchasing Pharmaceutical Assets in Development.

Bill Brastow, Ph.D., CTO, Market Modeling, Rosa & Co LLC, San Carlos, CA
Wednesday, August 17, 2022, 9:00 to 10:00 am PDT

Register for free at https://www.rosaandco.com/webinars

Abstract:
When performing due diligence for in-licensing, partnering, or purchasing 
pharmaceutical assets in development, pharmaceutical and biotech companies 
evaluate the asset based on factors including the scientific data available, 
intellectual property of the asset, clinical development plan, competitive 
analysis of the commercial opportunity for the asset and a financial analysis 
related to revenue projections.

Companies may attempt to complete this effort on their own or they may choose 
to use outside consulting firms to assist with components of the due diligence 
process.

This webinar will focus on how pharmaceutical and biotech companies can inject 
reality into the commercial opportunity analysis by measuring expected 
physician demand for the drug to inform revenue projections and decisions about 
in-licensing, partnering, or purchasing these assets.



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