Pharma-Intelligence

Pharma Intelligence & Automation
Transforming Complex Pharmaceutical Data Into Actionable Intelligence

kelectron pharma NPD

New Product Development (NPD) Tracking & Automation Software

Purpose:

Replace status-update emails and scattered Excel trackers with one custom NPD software built for how your company actually works — so every product’s current stage is visible on a single board, and no one has to ask.

Features:
  • Custom-built NPD tracking software, designed around your company’s own stages, approvals, and sign-offs — not a generic template.
  • Higher management gets real-time visibility into where each product stands, without chasing teams for updates.
  • Configurable to your existing NPD workflow and stage-gate process, not the other way around.
kelectron usfda helath caneda

Custom Regulatory Approval Dashboards — USFDA, Health Canada, EU & Japan

Purpose:

We know exactly where each regulatory authority publishes its approvals — USFDA, Health Canada, EMA/EU national agencies, PMDA Japan, and more — and we build that knowledge into a custom board so your team can see, at a glance, which drug got approved, by whom, and where, without visiting a single agency site.

Features:
  • A single custom dashboard maps every new approval to the product, applicant, and country automatically.
  • Built around how your team already works: filter by molecule, company, therapy area, or region in one screen.
  • Extendable to any additional region or authority your business needs, on request.
kelectron_patent_analysis

Patent Intelligence & Claims Mapping

Purpose:

Understand not just when a patent expires, but what it actually protects — so freedom-to-operate and NPD calls are made on claim scope, not headline dates.

Features:
  • Claim-by-claim reading and charting: composition, process, polymorph, formulation, and method-of-use claims separated out.
  • Patent-to-product mapping using IUPAC name and SMILES structure matching, not keyword search.
  • Para IV / litigation and settlement tracking for first-to-file opportunity assessment.
kelectron iqvia sales

Sales & Volume Data Automation (IQVIA / Symphony)

Purpose:

Remove the manual effort of cleaning and reconciling market data, and put trend-ready numbers in front of commercial teams every cycle.

Features:
  • Brand vs. generic volume-value trend dashboards, refreshed on your reporting cadence.
  • Therapy-area and competitor benchmarking without manual pivot-table rebuilding.
  • Market share, TRx/NRx, and channel-level tracking by molecule, brand, and therapy area.
kelectron pharma regulatory

Competitive & Business Intelligence Dashboard

Purpose:

Convert deep domain research into dashboards each function can actually use — without needing an analyst to translate it first.

Features:
  • Purpose-built views for BD, Regulatory Affairs, R&D, and Commercial teams from the same underlying data.
  • Custom KPI tracking by therapy area, molecule, or manufacturing site.
kelectron site establishment

Manufacturing Site & Capability Mapping Software

Purpose:

We build a custom software for your company that brings every site’s product, capability, and regulatory standing into a single window — so your team never has to check multiple registers or files to know which site can make what.

Features:
  • Site-to-product-to-approval linkage built from regulatory filings and facility registrations, shown in one screen.
  • Inspection history, 483 observations, and warning letter status attached directly to each site, not tracked separately.

Benefits for Pharma Companies

  • Know exactly which stage every product is at — no more emailing teams for status updates.
  • Give management a single board to check progress instead of chasing Excel sheets and mail chains.
  • Every model is checked by people who understand pharma terminology and workflow.
  • Outputs are dossier- and board-ready, not raw data dumps.
  • BD, RA, R&D, and Commercial work from the same source of truth.
  • Custom alerts keep every function focused on what matters to them.
  • Automated, reconciled IQVIA/Symphony trends — no manual rebuilding each cycle.
  • Consistent TRx/NRx and market-share views across brands and geographies.

Technical Architecture (High-Level Overview)

Data Collection Layer:
  • USPTO, EPO, and national patent office feeds.
  • USFDA Orange Book, Health Canada, EMA, and PMDA filings.
Processing & Normalization Layer
  • NLP-based patent claim parsing and charting.
  • Entity resolution across molecule, brand, and site records.
Analytics Layer
  • Our software team turns that logic into automated calculators, so the same expert judgment runs every time, without manual rework.
  • You get analysis built by people who understand pharma, delivered through software that scales it across your entire portfolio.
Delivery Layer
  • Our software team builds that into role-based dashboards, so each department opens exactly the view relevant to them.
  • Where needed, we connect the same intelligence directly into your ERP, PLM, or BI systems, so it fits into how your company already works.