Discover our Services
To support small startups, midsize Biotechs and fast-turnaround studies for large Biotechs or Pharma and Academic center clients, we offer a ONE-STOP All shopping services through unique network of Analytical, Biology and Pathology CLIA-Approved Laboratories with a CRO-grade quality data generation.
We support Conceptual, Mechanism of Action (MoA), Disease Modeling, Pharmacological efficacy, Biocompatibility, Pharmacokinetics, Toxicology (early drug development), Safety Pharmacology, Bioanalytical, and AI-driven Clinical Trial predictive modeling.
Our expert team is comprised of pharmacologists, drug and medical device developers, molecular biologists, toxicologists, bioinformaticians, medical writers, multilingual technical document writers, CME educators, and nutrition technologists.
At the Polycomb Scientific Solutions Group, we push the boundaries of discovery with cutting-edge technology and innovative thinking. Our team transforms visionary concepts into groundbreaking solutions, redefining the future of scientific exploration.
We support Food, Supplements, Pharma and Diagnostics development companies with ingredient safety risk-assessments, documentation, and regulatory readiness.
We provide services for designing, reviewing, and troubleshooting new or ongoing nonclinical studies. We support discovery, clinical development thru FIH stages of drug and molecular diagnostics development.
Core services include Risk Assessment, ingredient safety, Label/Compliance review per FDA/FTC guidelines, Regulatory Documentation review/defense, interpretation of data
We have expertise in Bridging Preclinical to IND/NDA stage; applying Pharmaceutical grade rigor to supplement industry; Ensuring alignment of devices or personal care products to ICH/ISO guidelines; and OECD Standard compliance for Assay/test validation.
Why work with us
Available for immediate project-based and short-term engagements
Scientific rigor with practical, business-focused recommendations
Experience bridging CRO-level analysis with industry needs
Fast turnaround for time-sensitive product launches
Cost-effective alternative to large consulting firms
Drug Development & Medical Device Safety Study Design Services
Our expert team of Molecular Pharmacologists and Toxicologists provides consultation services as follows:
(i) Design experimental plans, and procedures, and perform data analysis for new and ongoing Discovery, Preclinical and Clinical drug development studies.
(ii) Design PKPD, Toxicology, and Efficacy studies in Non-human Primate (Monkey), Dog, Rodent (transgenic, humanized), and Rabbit models for drug development
(iii) Address challenges on completed Preclinical and Pre-Phase 1 studies with RNAi, small molecules, antibody, ADC and immunotherapies.
(iv) Consultation on In vitro cell- assay development and In silico modeling of drug-target interaction.
(v) Biocompatibility risk assessment of medical devices and health products
Regulatory Documentation, Medical Writing and Grants/Scientific Reports Review
Our team comprises experts with a proven record of authoring Scientific Manuscripts, Grant Funding Applications and Industry Study reports.
(i) We provide services to review and edit data-based scientific manuscripts, National/International Grant Applications
(ii) We review and edit Preclinical Project Study reports for Academic, Start-up companies, CROs, the Pharmaceutical industry, Clinical Scientists, and Organizations.
(iii) We provide multilingual (English, Spanish, Arabic, Hindi) Scientific Courses and Training Material for University Students and Faculty on our platform.
Technology Transfer, CRO Services and Clinical Solutions
We provide CLIA-laboratory services and AI-powered solutions for Discovery to Clinical development Projects.
(i)Realizing the budget constraints of small and midscale scale Startups, we provide affordable access to pathology, In vitro, and AI-powered discovery stage and clinical trial solutions.
We provide access to CLIA-certified laboratories for early discovery and diagnostic needs. This includes in vitro and in vivo data generation.
We provide access to AI-powered platforms for clinical trials and Machine learning models simulating trials.
We provide access to AI-powered Wellness solutions to health centers.
(ii) We acquire emerging technologies and partner with VCs in drug & medical devices.
(iii) We are liaisons between startups, midsize pharma, and health centers for Contract Research services.
Contact us
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