Fake Medicine Check, Drug Approval & Quality Control System in Pakistan | VerifyPharma

⚡ 15,000+ Pharma Professionals
4.6 ⭐ Capterra 4.9 ⭐ G2

AI-Powered Pharma Ecosystem: Fake Medicine Detection, Quality Control & Drug Approval System for Biotechnology companies

Welcome to VerifyPharma - the first pharma ecosystem in Pakistan that brings together four essential solutions under one roof. Whether you want to check fake medicine by scanning QR code, get drug approval help from DRAP/FDA, implement a quality control system for your pharmaceutical company, and enroll in regulatory affairs training,we have you covered. Our AI-powered platform also supports Urdu voice assistant for local users.

🔬 QC System
Batch traceability
GMP compliance
COA validation
📋 Regulatory
Drug approval
FDA/DRAP/EMA
Submission readiness
🛡️ Verification
Fake detection
QR scan
Drug authenticity
0+
Drugs in Database
0+
Pharma Companies
0%
Prediction Accuracy
AI Pharmaceutical Platform - Drug Verification Dashboard
Live Scan Active
QC Passed
AI Analysis
✓ ISO 13485 • FDA • EU GMP
🤖 AI-Powered • Urdu Voice
👤 Patients → Verify medicine authenticity 🏭 Pharma → Improve drug approval success 🧑‍⚖️ Regulators → Evaluate compliance

Complete Pharma Quality & Regulatory Platform
for Every Team

One integrated solution for Quality Assurance, Regulatory Affairs, Manufacturing, R&D, and Management.
Trusted by 200+ pharma companies across 15 countries for medicine verification, GMP compliance, and drug approvals.

🟧 Fake Medicines: A Growing Concern in Pakistan

According to the World Health Organization (WHO), 1 in 10 medical products in developing countries is counterfeit. In Pakistan, this number can be higher in certain areas, putting millions at risk. The WHO Pakistan Office reports that certain regions may see rates as high as 30% for specific drug categories.

What makes a medicine fake?
No active ingredient • Wrong dosage • Toxic substances • Expired ingredients
Real impact on people
Treatment fails • Money wasted • Health worsens • Trust erodes
Pakistan-specific situation
DRAP alerts • Painkillers • Diabetes • Cancer treatments
Who benefits from medicine verification
Patients • Pharmacists • Providers • Distributors • Regulators
No active ingredient
Wrong dosage
Toxic substances
Expired ingredients
Fake Medicine Detection
⚠️ 30% counterfeit in certain areas

🟩 Three Platforms, One Ecosystem

Each platform addresses a specific need, but they work together seamlessly as a complete pharmaceutical software platform.

✅ VERIFY PHARMA: Medicine Authentication

What it does: Instantly verifies whether a medicine is authentic, expired, or fake — using just a QR code or batch number. Our fake medicine detection system uses AI-powered image recognition for instant results.

Perfect for:

• Pharmacists • Patients • Distributors • Regulators • Healthcare providers

How it works in Pakistan:

1. Scan QR code using medicine barcode verification
2. Or manually enter batch number
3. System checks against DRAP database
4. Result in under 10 seconds

Key features:

• QR/barcode scanning • Batch verification • Expiry date checking • Fake reporting to DRAP • Urdu language support

Real-world use: A pharmacy in Karachi verified 500 medicines last month and identified 12 counterfeit products — all reported through the system.

🏭 QUALITY CONTROL: For Manufacturers

📋 REGO: AI-Powered Regulatory Affairs

🤖 ARTIFICIAL INTELLIGENCE

AI Across All Platforms

What makes this ecosystem different is how AI is integrated throughout — from verification to training.

Verify Pharma AI

  • Image recognition for QR/barcode scanning
  • Pattern matching for fake medicine detection
  • Predictive alerts for expiry dates
🔬

Quality Control AI

  • Anomaly detection in manufacturing
  • Predictive maintenance for equipment
  • Document OCR for scanned records
📋

REGO AI

  • Objection prediction (10,000+ cases)
  • Similarity checking (98% accuracy)
  • Regulator simulator (DRAP, FDA, EMA)
  • Voice assistant in Urdu & English
🎓

REGO Academy AI

  • Personalized learning paths
  • Progress tracking & recommendations
  • Skill gap analysis for career growth

How AI is trained

50K+
Drug samples
10K+
Regulatory submissions
5K+
Objection cases
Millions
QC data points
Thousands
Training hours & assessments

"AI doesn't just automate — it anticipates and educates. Instead of reacting to problems, you prepare for them — and train your team to do the same."

🎓 REGO ACADEMY: Training the Next Generation of Pharma Professionals

REGO isn't just a tool — it's a complete education platform designed for the entire pharma community.

📋

Document Control

Centralize and control documents with version control, e-signatures, and audit trails.

Version Control E-signatures Audit Trails
🎓

Training Management

Automate training activities, maintain controlled training records, and track staff competence.

Staff Competence Training Records Automated Tracking
🔄

Change Management

Streamline change control from request submission through review, approval, and implementation.

Change Control Approval Workflow Implementation
⚙️

Design Control

Control and document design activities to manage risk and meet regulatory requirements.

Risk Management Documentation Compliance
⚠️

Deviation Management

Track and manage deviations, non-conformances, and CAPA activities with full traceability.

Non-conformances CAPA Traceability

✨ Success stories:

"REGO Academy helped me transition from quality control to regulatory affairs. The certification gave me credibility with employers."

— Ayesha Khan, Regulatory Affairs Officer

"Our entire QA team trained on GMP compliance through REGO. We passed our DRAP inspection with zero observations."

— Omar Farooq, Plant Manager

Who benefits from REGO Academy:

Audience
What They Gain
Regulatory affairs
Certification, updated knowledge
Quality control officers
GMP training, best practices
Biotech researchers
Approval pathways, intelligence
Microbiologists
Contamination control, protocols
Pharmacy students
Career prep, practical knowledge
Manufacturing teams
Quality systems, audit readiness
Industry professionals
Continuing education credits

What's included:

Video courses (En/Ur)
Interactive quizzes
Certification programs
Job board
Webinars with experts
Case studies

🤖 AI-powered learning

Personalized paths based on your role, goals, skills, and industry trends.

👤
For Patients
Verify medicine authenticity
🏭
For Pharma Companies
Improve approval success & quality
🧑‍⚖️
For Regulators
Evaluate compliance & safety

Trusted by 200+ FDA-Compliant Pharmaceutical Companies

verifypharma helps life science companies ensure compliance with FDA, ISO, EU, GxP, and other regulatory requirements through a fully validated eQMS trusted by industry leaders.

Trusted by leading pharmaceutical companies worldwide

ISO 13485:2016
Medical Devices
ISO/IEC 27001:2022
Information Security
FDA 21 CFR Part 11
Electronic Records
FDA 21 CFR Part 820
Quality System
FDA 21 CFR Part 211
GMP for Drugs
FDA 21 CFR Part 212
PET Drugs
FDA 21 CFR Part 4
Combination Products
FDA Data Integrity
ALCOA+
EudraLex Volume 4
GMP Guidelines
GMP Annex 11
Computerized Systems
Eudralex
EU Pharmaceutical Law
EU MDR
Medical Devices
EU IVDR
In Vitro Diagnostics
UK MDR
UK Medical Devices
ISO 14971:2019
Risk Management
GMP
Good Manufacturing Practice
IEC 60601
Medical Electrical Equipment
IEC 62304
Medical Device Software
ISO 1518:2022
Medical Laboratories
ISO 16085:2021
Risk Management
ICH Q10
Pharmaceutical Quality System
ICH Q9
Quality Risk Management
CLIA
Laboratory Standards
15,000+ Pharma Professionals
4.6 Capterra
4.9 G2
Activate Windows Go to Settings to activate Windows.

Trusted by Pharma Industry Worldwide

Our platform is trusted by pharmaceutical companies, regulatory bodies, and healthcare professionals across the globe.

🇵🇰

Pakistan

DRAP

🇺🇸

United States

FDA

🇪🇺

Europe

EMA

🇬🇧

United Kingdom

MHRA

🇸🇦

Saudi Arabia

SFDA

🇦🇪

UAE

MOHAP

🇰🇷

South Korea

MFDS

🇯🇵

Japan

PMDA

ISO 13485:2016 ISO 27001:2022 FDA 21 CFR Part 11 EU GMP Annex 11 WHO GMP
0
Medicines Verified
0
Drug Submissions Tracked
0
Countries Covered
0
Customer Satisfaction
0
Average Time Saved
0
Professionals Trained

What users say

"REGO helped us anticipate objections and prepare responses in advance. Our biosimilar was approved in 11 months instead of the usual 18."

AR

Dr. Asim Raza

Regulatory Head, ABC Pharma

"The quality control system made our DRAP inspection completely smooth. Every document was ready, every batch traceable."

KM

Mr. Khalid Mahmood

Plant Manager, XYZ Pharma

"As a pharmacist, I verify 50+ medicines daily. This system catches fakes instantly."

FK

Dr. Fatima Khan

Community Pharmacist, Lahore

"REGO Academy transformed our team's capabilities. The certification program is world-class."

NA

Dr. Nida Ali

Training Manager, PharmaTrain

READY TO GET STARTED?

Choose your entry point:

🔍
Checking a medicine
🔍 Verify Now – Free
🏭
Manufacturing quality
🏭 Request QC Demo
📋
Drug approval assistance
📋 Start REGO Free Trial
🎓
Pharma training
🎓 Explore REGO Academy
All platforms accessible via web and mobile. 24/7 support included.

🟫 Frequently Asked Questions

Quick answers to common questions about medicine verification, drug approval, and our platforms.

❓ How do I check if my medicine is original in Pakistan?
❓ What is DRAP's role in medicine verification?
❓ How long does drug approval take in Pakistan?
❓ Can small pharma companies afford this?
❓ Is Urdu supported?
❓ How accurate are objection predictions?
❓ Where can I report fake medicine in Pakistan?
❓ What countries does REGO cover?
❓ Do you offer a medicine barcode verification API?
❓ Who can benefit from REGO Academy?

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