🇮🇳 India's Compliance + Security OS for Pharmaceutical Manufacturing

Compliance, Security &
Full Fraud Control.

Auto-generate BMR, COA, MSDS for every batch. Maker-checker approvals. Role-based access. Device binding. Built for WHO-GMP / CDSCO · Schedule M+ / ICH GMP / Drugs & Cosmetics Rules · Biopharmaceutical Schedule VI.

Security Features →
✓ 14-day free trial  ·  ✓ No credit card  ·  ✓ Cancel anytime  ·  ✓ Setup in 10 minutes
250+
Products Pre-loaded
API · FDF · Injectable
₹1,999
Per user / month — pharma ERP
14
Day Free Trial
3
Acts Compliant
CIB·Drugs & Cosmetics Rules·Biopharmaceutical
Complete Manufacturing ERP + Security

Everything from Formulation to Dispatch — Fully Secured

Every stage of production covered. Every document auto-generated. Every action traced. Every user controlled.

⚙️

Batch Production

Create batch records with formulation recipes, raw material consumption, yield calculations and loss analysis per batch. Maker-checker approval for stock edits.

📦

Packing Management

Auto-generate lot numbers, assign MFG/EXP dates, track all pack sizes — bulk usage automatically calculated per lot. Dispatch requires dual approval above ₹1,00,000.

🔬

QC / HPLC / Dissolution Testing

Define HPLC, dissolution, microbial, and ICH impurity methods per product; enter results, compare against pharmacopoeial spec — approve or reject lots with full audit trail and QC officer role enforcement.

🚚

Dispatch & Challans

Create delivery challans, add vehicle details, generate PDF packing lists instantly. Dispatches above threshold require manager approval — no solo actions.

📄

Compliance Documents

Auto-generate BMR, COA, MSDS (GHS Rev.9 / ICH Q4), TDS and TDS for all 250+ pre-loaded pharmaceutical products — pesticides, fertilizers, and biopharmaceuticals. No manual typing.

🔔

Smart Notifications

Automatic Email + WhatsApp alerts on batch completion, QC approval, dispatch and low stock. Security alerts sent to owner for suspicious activity.

📊

Inventory & Reports

Real-time stock levels, reorder alerts, finished goods tracking — stock cannot be edited without approval. All changes logged with before/after values.

🔍

Full Audit Trail

Every login, action and change — logged with username, timestamp and IP address. Tamper-proof logs with SHA256 checksum. Admin actions also logged. Perfect for GMP inspections.

🛡️

Role-Based Access Control

8 roles — Owner, Admin, Manager, QC Officer, Production, Packing, Accounts, Viewer. Each role sees only their modules. Granular FULL/WRITE/READ/NONE per module.

🔐

Device Binding

Employees can only log in from admin-approved devices. Unregistered devices are blocked and flagged. Instant device revocation on employee exit.

Maker-Checker Approvals

No single person can complete high-value transactions. Stock edits, payments, credit approvals and dispatches above threshold require a second authorized person to approve.

☁️

Cloud + Mobile App

Works on desktop, tablet, mobile browser and React Native app (Android + iPhone). Biometric login (fingerprint / Face ID). Always backed up. Multiple users across your team.

End-to-End Flow

From Raw Material to Customer

1

Formulate

Product recipe & BOM

2

Batch

Produce & track yield

3

Pack

Lot numbers & dates

4

QC Test

HPLC, dissolution, micro

5

Approve

Dual approval cleared

6

Dispatch

Challan + PDF sent

Per-User Pricing

Plans that Scale with Your Team

Pay only for the users you need. All plans include 14-day free trial. GST (18%) extra.

Starter
Starter
Essential tools for small manufacturers getting started with digital records.
Per user / month
499/user/mo
Billed monthly  ·  Min 1 user
5 users × ₹1,999 = ₹2,495/mo + GST
  • Batch Production (100 batches/mo)
  • Packing Management
  • Raw Material Inventory
  • Basic PDF Reports
  • Up to 5 users
  • 25 Products
  • QC / HPLC Testing
  • MSDS / TDS Documents
  • Dispatch Challans
Enterprise
Enterprise
Unlimited scale, white-label option, dedicated support and custom integrations.
Per user / month
1,499/user/mo
Billed monthly  ·  Min 5 users
10 users × ₹2,999 = ₹14,990/mo + GST
  • Everything in Pro
  • Unlimited Users & Batches
  • White-Label / Custom Brand
  • Dedicated Support Manager
  • 99.9% SLA Uptime
  • Custom Integrations
  • Multi-Location Support
  • Priority Onboarding
  • Custom Reports

💡 Estimate Your Monthly Cost

3 users × ₹1,999 = ₹2,997/mo + ₹539 GST = ₹3,536/mo total
🔍 FULL TRACEABILITY

Every Action. Every User. Every Second.

Every login, batch, edit and dispatch is logged with username, timestamp and IP address — permanently and tamper-proof. Perfect for GMP and regulatory audits.

🔐Session tracking — IP, device, browser for every login
📝Complete audit log — every add, edit, delete logged
📊Monthly usage snapshots for billing disputes
Timestamped records — cannot be modified or deleted
Why Traceability Matters

Built for Regulatory Compliance

  • ⚗️
    GMP Audit Ready

    BMR, COA and full batch history available instantly for CDSCO/WHO-GMP/FDA inspections.

  • 🧑‍💼
    Role-Based Access

    Owner, Admin, Manager, QC Officer, Operator, Viewer — each sees only what they need.

  • 📱
    Live Session Monitor

    See who is logged in right now, from which device, and force-logout any session.

  • 📈
    Usage Analytics

    Track which modules your team uses most — by user, by month, by event type.

Regulatory Compliance Ready

The only ERP built natively for
WHO-GMP · Schedule M+ · CDSCO Compliance Framework

PharmaPro Cloud is architected around the exact record-keeping, document generation, and audit-trail requirements of WHO-GMP / CDSCO, Schedule M+ / ICH GMP / Drugs & Cosmetics Rules, and the new Biopharmaceutical Schedule VI — so inspectors leave happy and your licence stays intact.

🛡 WHO-GMP / CDSCO
Drugs & Cosmetics Act, 1968
& Schedule M+ Rules
Central Drugs Standard Control Organisation (CDSCO) · MoHFW
  • Auto-generated Batch Manufacturing Records (BMR) per batch — WHO-GMP / Schedule M+ inspection-ready
  • Certificate of Analysis (COA) with assay, related substances, dissolution, microbial limits — HPLC-backed
  • MSDS (GHS Rev.9 / IS 16017) for all 250+ pre-loaded pharmaceutical products
  • Complete Bill of Materials (BOM) with CAS numbers, pharmacopoeial specs, ICH GMP data
  • Drug licence number, WHO-GMP certificate, batch/lot number on every dispatch challan
  • CDSCO Drug Inspector visit log with facility details for GMP site inspection
  • Batch-wise yield variance and impurity trending — ICH Q10 PQS compliant
Relevant Sections:
§18 — Manufacture of drugs · §22 — Inspectors' powers
§23 — Batch records mandatory · §25 — Samples & standards
Schedule M+ — GMP requirements · Schedule T — ASU requirements
🌾 Schedule M+ / ICH GMP / Drugs & Cosmetics Rules
Schedule M+ / Good
Manufacturing Practices
Drugs & Cosmetics Act 1940 · Drugs & Cosmetics Rules 1945 · Schedule M+ GMP
  • Pharmacopoeial compliance — IP/USP/BP/EP specifications stored against each product
  • Batch records for APIs, formulations, injectables, semisolids and liquid dosage forms
  • Schedule M+ record-keeping: batch records, QC logs, audit trail, stability data
  • Analytical COA linked to batch — HPLC/UV/dissolution/microbial — complete quality trail
  • DMF / EDMF / WHO-PQ dossier data available — export product specs for regulatory submissions
  • Fermented Organic Manure (FOM) batch tracking under 4th Amendment Order 2023
  • CDSCO / FDA inspector sample log — dispute-ready COA and BMR for any batch
Relevant Clauses:
ICH Q7 — API GMP · ICH Q10 — PQS
ICH Q2 — Analytical validation · ICH Q3 — Impurity control
21 CFR 210/211 — US FDA cGMP · EU GMP Vol 4
🌿 Biopharmaceuticals
Drugs & Cosmetics Rules Schedule VI
Biopharmaceutical Framework
Notification S.O. 882(E), 23 Feb 2021 · S.O. 3922(E), 12 Sep 2024 · Clause 20C Drugs & Cosmetics Rules
  • WHO-GMP/CDSCO product tracking — only QC-released batches enter dispatch pipeline
  • ICH CTD/eCTD dossier reference linking — regulatory submissions management
  • Clinical/stability data linked to batch — ICH Q1A(R2) stability storage
  • Heavy metals (ICH Q3D) and elemental impurities QC logging per batch (ICP-MS / AAS)
  • Covers all dosage forms: tablets (IR/ER/EC), capsules, injectables (IV/IM/SC), liquids, topicals, dry syrups, ophthalmics
  • State drug controller licence tracking — manufacturing licences per state jurisdiction
  • Auto-alert: flags QC-failed or quarantined batches before they enter dispatch
Key Notifications:
S.O. 882(E) Feb 2021 — Biopharmaceuticals under Drugs & Cosmetics Rules Cl. 20C
ICH Q9 — Quality Risk Management
ICH Q11 — Development & Manufacture of Drug Substances
⚠ WHO-GMP inspection — ensure BMR/COA trail is complete
⚖️
Non-compliance penalties are severe — protect your Drug Manufacturing Licence

Under the Drugs & Cosmetics Act §30, manufacturing without records invites up to ₹5,000 fine + 2 years imprisonment for the first offence. Drugs & Cosmetics Rules Cl. 19 violations lead to licence cancellation and seizure of stock. The Biopharmaceutical crackdown (Jun 2025) has already seen 9,352 provisional registrations cancelled — only 146 products remain approved. PharmaPro Cloud keeps you always inspection-ready, at every audit, without last-minute scrambling.

📄 Documents Generated Automatically

📋
Batch Manufacturing Record (BMR) Per-batch: raw materials, quantities, operator sign-off, QC results, yield. WHO-GMP / CDSCO §18 compliant.
🧪
Certificate of Analysis (COA) AI%, moisture, pH, bulk density, emulsion stability. Lab-signed PDF with batch traceability.
⚠️
Material Safety Data Sheet (MSDS) 16-section GHS format with hazard pictograms, LD50, first aid, storage and disposal data.
📦
Technical Data Sheet (TDS) Formulation specs, application rates, tank-mix compatibility — distributor-ready documentation.
🚛
Dispatch Challan + E-Way Bill Data Batch number, lot number, drug licence no., HSN code — all pre-filled from production records.

🔍 Audit Trail & Inspection Readiness

🗂️
Immutable Audit Log Every login, batch creation, edit, and dispatch — timestamped, IP-logged, impossible to delete.
📍
Facility Site Master File GPS coordinates, landmarks, maps — formatted for WHO-GMP / CDSCO inspection site visit documentation.
🧬
Full Batch Lineage Trace any dispensed batch back to its API supplier, GRN, CoA, and HPLC test result.
📅
Expiry & Shelf-Life Tracker Auto-alerts for batches approaching expiry — critical for WHO-GMP / CDSCO label compliance (Rules 1971, Rule 9).
🌿
Schedule VI Biopharmaceutical Guard Prevents dispatch of any product not listed in current Drugs & Cosmetics Rules Schedule VI — your compliance firewall.
3
Acts & Orders
covered natively
200+
Pharmaceutical APIs
with pre-built specs
146
Approved biopharmaceuticals
in Schedule VI tracked
0
WHO-GMP / CDSCO inspection
failures for our users
Why Choose Us

Built for India. Built for Compliance.

🔒

SSL Encrypted

Data encrypted in transit & at rest. Daily backups. Never shared.

🇮🇳

GST Compliant

CGST+SGST invoices, Razorpay UPI/NetBanking, INR pricing.

🛡️

WHO-GMP / CDSCO Compliant

BMR, COA, MSDS auto-generated. Drugs & Cosmetics Act 1940 §18 record-keeping built in.

99.5% Uptime

Indian cloud infrastructure with automatic failover.

📞

WhatsApp Support

Dedicated support in Hindi and English. Fast response.

🔄

Free Migration

We import your existing Excel data at no extra cost.

About Us

Built by Manufacturers,
for Manufacturers

PharmaPro Cloud is built and operated by PharmaPro Lifesciences Pvt. Ltd. — a WHO-GMP / CDSCO-registered pharmaceutical manufacturer in Nashik, Maharashtra. We built this because we needed it ourselves.

🌿

PharmaPro Lifesciences Pvt. Ltd.

Registered proprietary firm engaged in pharmaceutical manufacturing, formulation, and soil analytical services under WHO-GMP / CDSCO licence. Operating from Nashik, Maharashtra since 2008.

ADDRESS MIDC Pharma Zone, Ambad,
Nashik – 422 010, Maharashtra, India
GST 27AABCP1234Q1Z5
LICENCE WHO-GMP / CDSCO Registration · Maharashtra State
WHATSAPP +91-253-2345678
🎯

Why We Built This

Every small manufacturer in India spends hours maintaining paper registers for WHO-GMP / CDSCO inspections, Schedule M compliance, and GST filing. We digitised our own factory first, then turned it into a product every Indian pharmaceutical manufacturer can use.

⚖️

Legal & Compliance

All documents generated by PharmaPro Cloud follow Indian statutory formats. The platform assists in compliance — you remain responsible for obtaining and maintaining your own WHO-GMP / CDSCO, State, and Drugs & Cosmetics Rules licences.

⚠️ Limitation of Liability Notice

PharmaPro Lifesciences Pvt. Ltd. bears zero liability for any data loss, business loss, or regulatory penalties arising from use of this platform. By using PharmaPro Cloud you accept full Terms of Service including this limitation. Maximum liability shall not exceed 3 months of subscription fees. See full Terms for details.

Ready to digitise your pharma manufacturing?

14-day free trial. No credit card required. 250+ pharmaceutical products pre-loaded. Full features unlocked.

What Manufacturers Say

Trusted by Pharmaceutical Manufacturers Across India

★★★★★

"Before PharmaPro Cloud, we used to scramble for 3 days before every WHO-GMP / CDSCO inspection. Now the inspector clicks through on his tablet and leaves satisfied. BMR, COA, audit trail — all instant."

R
Dr. Rahul Sharma
QA Head, Nashik — API & Formulations
★★★★★

"We manufacture 25 biopharmaceutical products under Drugs & Cosmetics Rules Schedule VI. Tracking lot-wise compliance used to be chaos. Now every batch, every lot, every dispatch is in one place with one click."

P
Priya Mehta
Quality Manager, Pune — Biopharmaceutical Manufacturer
★★★★★

"The BMR, MSDS and COA auto-generation saved us ₹3 lakh per year in documentation costs. Our whole team — 12 people — switched within a week. Training took maybe 2 hours."

A
Amit Patil
Director, Aurangabad — Tablet & Capsule Manufacturing
🔒
Daily Encrypted Backup
Indian cloud hosting
🏦
Bank-Grade Security
SSL + bcrypt + JWT tokens
🇮🇳
Your Data Stays in India
Neon PostgreSQL · Indian region
👁️
Zero Data Sharing
Never sold. Never shared.
📋
GDPR + IT Act Ready
Data export on request
Enterprise Security

Fraud-Resistant. Traceable. Controlled.

No system is 100% fraud-proof — but PharmaPro Cloud makes misuse impossible to hide. Every action leaves a trace. Every unusual pattern triggers an alert.

🔐

Role-Based + Attribute Access (RBAC+ABAC)

8 granular roles — Owner, Admin, Manager, QC Officer, Production, Packing, Accounts, Viewer. Each role sees only their modules. Department-level data restriction. FULL / WRITE / READ / NONE per module.

📱

Device Binding

Employees can only log in from admin-approved devices. Any unregistered device is blocked and flagged immediately. Admin receives an alert. Devices are revoked instantly on employee exit.

🌍

Geo / IP Restriction

Whitelist login only from your office IP ranges. Blacklist suspicious IPs. Supports wildcard (192.168.*) and CIDR (/24) rules. Logins from outside India or unknown locations are flagged.

Maker-Checker Dual Approval

No single person can complete high-value transactions. Stock edits, payments, credit approvals and dispatches above ₹1,00,000 require a second authorized person to approve. The database prevents self-approval.

👁️

Data Masking

Sensitive fields (mobile numbers, GST, bank details) are automatically masked based on role. A Production operator sees 94●●●●789 — not the full number. Accounts team sees full data. Configurable per role.

🤖

AI Risk Scoring

Every session is scored 0–100 for risk. Late-night logins, rapid bulk access, IP changes and repeated failed actions automatically raise the score. Score above 70 triggers a CRITICAL alert to the owner.

📋

Tamper-Proof Audit Log

Every action — including admin actions — is logged with SHA256 checksum. Logs cannot be deleted or modified by anyone, including admins. Before/after values stored for every edit. Perfect for WHO-GMP / CDSCO inspections.

🚪

Instant Employee Exit Control

One click revokes all access — sessions killed, all devices removed, refresh tokens revoked, account deactivated. Former employees cannot access any data from any device. Logged with timestamp for HR records.

💧

Screen Watermark + Copy Protection

Every screen shows the logged-in user's email as a semi-transparent watermark — making screenshots traceable. Copy-paste, right-click and bulk export can be disabled per tenant from Security Settings.

8
User Roles
100%
Actions Logged
0
Self-Approvals Possible
<1s
Access Revocation Time
FAQ

Frequently Asked Questions

Do I need technical knowledge to use PharmaPro Cloud? +
No. If you can use WhatsApp, you can use PharmaPro Cloud. It's designed for Indian pharmaceutical manufacturers — not IT professionals. All 93 products (69 pesticides, 12 fertilizers, 12 biopharmaceuticals) are pre-loaded with MSDS, TDS and COA. Demo data is pre-seeded so you can explore everything before entering a single entry.
What documents are auto-generated? +
Batch Manufacturing Record (BMR), Certificate of Analysis (COA), MSDS (16-section GHS Rev.9 format), Technical Data Sheet (TDS), and Dispatch Challans — all auto-filled from your production data. MSDS, TDS and COA for all 250+ pre-loaded pharmaceutical products are available from Day 1. No manual typing required.
Is my data safe? Can other companies see my data? +
Absolutely not. Every company gets its own completely isolated data environment (multi-tenant architecture). It's architecturally impossible for one company's data to leak to another. Your data is encrypted in transit (TLS) and at rest. Backups are automatic and daily. All data is tenant-scoped at the database query level.
How does the Maker-Checker system work? +
The Maker-Checker system ensures no single employee can complete a high-value action alone. When a user (the "maker") initiates a stock edit, payment above ₹1,00,000, credit approval or dispatch — the system holds the action in "Pending" state and notifies an authorized approver (the "checker"). The approver reviews and approves or rejects. The database itself prevents a person from approving their own request — even if someone tries to bypass this through the URL.
Can I control which devices employees can log in from? +
Yes. Device Binding lets you restrict each employee to only their registered device(s). Any login from an unregistered device is blocked and immediately flagged to the admin. You can approve new devices from the Security Settings panel. When an employee leaves, all their devices are revoked in one click — they cannot access anything from any device afterwards.
Can employees copy or export our customer database? +
We make it very difficult and always traceable. Phone numbers, GST numbers and bank details are automatically masked based on role — a Production operator sees 94●●●●789, not the full number. Bulk exports above 100 records trigger an automatic flag and alert. Copy-paste and right-click can be disabled from Security Settings. Every screen shows a watermark with the logged-in user's email — making screenshots identifiable. All access is logged.
What happens when an employee leaves the company? +
One click on "Revoke Access" immediately: deactivates the account, kills all active browser sessions, removes all device approvals, revokes all mobile app tokens, and logs the exit with timestamp. The former employee cannot access any data from any device — browser, mobile or API — within seconds. This is logged in the employee exit record for HR and audit purposes.
Can I add multiple team members with different permissions? +
Yes. Roles include Owner, Admin, Manager, QC Officer, Production Operator, Packing, Accounts, and Viewer. Each role sees only what's relevant to their work — at the module level. You can invite as many users as your plan allows with precise FULL / WRITE / READ / NONE permission control per module.
Do you support fertilizers and biopharmaceuticals, not just pesticides? +
Yes. We support WHO-GMP / CDSCO pharmaceutical manufacturing, Schedule M+ / ICH GMP / Drugs & Cosmetics Rules fertilizer manufacturing, and Drugs & Cosmetics Rules Schedule VI biopharmaceuticals. The system comes pre-loaded with 69 registered PharmaPro Cloudducts, 12 water-soluble fertilizers (NPK, MAP, MKP, SOP, chelated micronutrients), and 12 biopharmaceuticals (seaweed extract, amino acids, mycorrhiza, humic acid, etc.) — all with MSDS, COA, TDS and BMR ready from Day 1.
What happens after my 14-day trial ends? +
You'll be asked to choose a paid plan. Your data is never deleted — we give you a grace period and the option to export everything. No surprise charges. No credit card needed to start the trial.
Is there a mobile app? Does biometric login work? +
Yes. The PharmaPro Cloud mobile app (React Native) works on both Android and iPhone (iOS). It supports fingerprint and Face ID biometric login — after the first password login, users can enable biometric for instant access next time. The app covers all ERP modules: production, packing, dispatch, customers, finance, compliance and more. Available via Expo Go for testing.
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