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Lucid Biostatistical Consulting LLC.

Lucid Biostatistical Consulting LLC. is a consulting firm specializing in clinical trials and biostatistical research. We offer our clinical trials design and analysis services to pharmaceutical companies and medical devices companies. We offer the biostatistics research services to principal investigators of grant-funded studies and grant-writing services as well. Our consultants, all Ph.D.s, have extensive experience in their respective fields.

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Arkady Gershteyn

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Arkady Gershteyn

41 De●●●●●treet

Ne●●on , Massachusetts, 02461

United States

617●●●532
ar●●●●●●●@gmail.com

View this contact

Arkady Gershteyn

41 De●●●●●treet

Ne●●on , Massachusetts, 02461

United States

617●●●532
ar●●●●●●●@gmail.com

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Lucid Biostatistical Consulting LLC. | lucidbiostatistics.com Reviews
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Lucid Biostatistical Consulting LLC. is a consulting firm specializing in clinical trials and biostatistical research. We offer our clinical trials design and analysis services to pharmaceutical companies and medical devices companies. We offer the biostatistics research services to principal investigators of grant-funded studies and grant-writing services as well. Our consultants, all Ph.D.s, have extensive experience in their respective fields.
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1 biostatistics
2 statistics
3 clinical trials
4 research
5 medical research
6 pharmaceutical
7 consulting
8 clinical trial
9 clinical
10 monitoring
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Lucid Biostatistical Consulting LLC. | lucidbiostatistics.com Reviews

https://lucidbiostatistics.com

Lucid Biostatistical Consulting LLC. is a consulting firm specializing in clinical trials and biostatistical research. We offer our clinical trials design and analysis services to pharmaceutical companies and medical devices companies. We offer the biostatistics research services to principal investigators of grant-funded studies and grant-writing services as well. Our consultants, all Ph.D.s, have extensive experience in their respective fields.

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lucidbiostatistics.com lucidbiostatistics.com
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Lucid Biostatistical Consulting LLC.

http://www.lucidbiostatistics.com/index.html

Lucid Biostatistical Consulting LLC. Data Mining, Machine Learning, Statistical Learning. FDA Regulations for Clinical Trials. European Medicines Agency (EMEA) Regulations. FDA's Critical Path Opportunities List. Welcome to LBC LLC! High quality services by exceptionally experienced consultants. Project-based payment assures fast turn-around time. Clarity of presentation allows straighforward understanding of interpretation of results and premise for proposed analaysis methodology.

2

Lucid Biostatistical Consulting Clients

http://www.lucidbiostatistics.com/clients.html

Lucid Biostatistical Consulting LLC. FDA Regulations for Clinical Trials. European Medicines Agency (EMEA) Regulations. FDA's Critical Path Opportunities List. Our consultants have experience working with the following clients. Clinical Trials: Preclinical and Phase I-IV. Yale University School of Medicine. Albert Einstein College of Medicine. Nobel Prize committee of Medicine and Physiology. Stony Brook Medical Center. University of California - Irvine, School of Medicine.

3

Lucid Biostatistical Consulting Experience

http://www.lucidbiostatistics.com/experience.html

Lucid Biostatistical Consulting LLC. FDA Regulations for Clinical Trials. European Medicines Agency (EMEA) Regulations. FDA's Critical Path Opportunities List. Clinical Trials: Preclinical and Phase I-IV. Lead statistician for filing of 14 NDA (New Drug Application) /BLA (Biologic License Application) submissions in USA, Europe, and Japan. Twenty Five years of experience in pre-clinical and phase I-IV clinical trials of drugs and medical devices. Biostatistics therapeutic specialization in:. Expertise in...

4

Lucid Biostatistical Consulting Services

http://www.lucidbiostatistics.com/services.html

Lucid Biostatistical Consulting LLC. FDA Regulations for Clinical Trials. European Medicines Agency (EMEA) Regulations. FDA's Critical Path Opportunities List. Clinical Trials: Preclinical and Phase I-IV. Preparing Statistical Analysis Plans (SAP) – considering adaptive design. Statistical representation and presentation to regulatory authorities in USA and Europe (FDA, EMEA). Modeling and simulation of clinical data, and exploratory analysis of preclinical data.

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