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PharmNodeFormulation B2B SaaS
Digital Pharmaceutical Compounding

Virtual Formulation Studio for B2B Pharma & Supplements

Design formulations, calculate powder flowability, simulate tablet presses, verify regulatory limits, and generate GMP compliance reports in a real-time, node-based workspace.

Active Formula: Amlodipine_Besylate_v1.2
PRO SIMULATION ACTIVE
ActiveCAS: 111470-99-6

Amlodipine Besylate

Input percentage:12.5%
Blending Node99.8% flowability

Blending

Hausner Ratio:1.09 (Excellent)
Raw cost:$12.40 / kg
Tablet PressPorosity: 18.4%

Punch 8.0 mm

Tablets output:85,200 шт.
Tablet weight:112.5 мг

All your calculations in a single visual workspace

We combine chemistry logic, physical properties simulation, and B2B pricing parameters into a powerful node-based canvas.

Node-Based Editor

Connect ingredients, adjust active pharmaceutical ingredients (APIs), and preview formulation components dynamically.

Physical Simulator

Instant calculations of Carr's Index, Hausner Ratio, bulk and tapped densities to ensure blend flowability.

Chemical Compatibility

Real-time verification of raw material conflicts. Detect amino-sugar browning and lactose allergen conflicts.

GMP Documentation

Generate strict regulatory PDFs containing technological instructions, safety sheets, and digital validator signatures.

From initial idea to tech spec in 3 simple steps

PharmNode streamlines drug design, replacing outdated Excel sheets with a digital decision support system.

  • 1. Select Active IngredientAdd substances with pre-populated CAS numbers, densities, and safe limits.
  • 2. Add Excipients & BindersTweak input percentages. The engine recalculates blend flowability and alerts you of errors.
  • 3. Press Simulation & GMP ExportSet punch dimensions, calculate tablet porosity, and export validated technological logs.
GMP Validation Report (Simulation)Document ID: US-21CFR-112
Ingredient Role Compatibility:COMPLIANT (100%)
Magnesium Stearate Hydrophobicity:Pass (1.2% ≤ 1.5% max)
Allergen Profile (FALCPA):Warning: Contains Milk (Lactose)
FDA Label Standard (21 CFR):Dietary Supplement Standard (US)
DSS Regulatory Notice

PharmNode acts as a Decision Support System (DSS). All formulas are predictive. Physical laboratory validation (FTIR, DSC, HPLC) is strictly required before scale-up and industrial manufacturing.

Built on State-of-the-Art Software Stack

We leverage industry-leading technologies to guarantee low latency, robust data storage, and compliance.

Next.js 16 & React 19

Fast hybrid server and client rendering with strict typing.

PostgreSQL & Prisma ORM

Safe relational storage of users, projects, and component schemas.

MongoDB Database

Flexible, high-performance storage for complex node-based canvas graphs.

Secure OAuth Security

Secure login utilizing NextAuth.js for corporate credentials.

Stripe Billing Engine

Instant subscription management for Pro and Enterprise plans.

Regulatory Compliance Standards

Our verification engine is engineered in collaboration with pharma consultants to comply with major legal environments.

FDA Title 21 CFR

Complies with digital signature requirements, dietary supplement labeling rules, and safe input thresholds.

EFSA Supplement Rules

Enforces metric parameters, EU allergens reporting, and EFSA maximum safe daily intake parameters.

Allergen Disclosures

Automatically profiles allergens and prints mandatory 'Contains' statements for allergens like lactose or gluten.

Ready to optimize your formulations?

Start designing in our sandbox immediately. No credit card required.