Compliance you can trust.
Software that works.
RS Technologies delivers Computer System Validation for HPLC, PLC, HMI, SCADA & Excel spreadsheets, supplies industrial hardware & electronics, installs CCTV camera systems, and builds GxP-ready software like Pharma Pilot, E-Logbook, E-BMR, HRMS, Training Module and Gate Management System.
- GAMP 5
- 21 CFR Part 11
- EU Annex 11
- ALCOA+
Validation, Automation & Hardware Services
Complete lifecycle support for your GxP computerized systems — from planning to periodic review.
Computer System Validation (CSV)
End-to-end CSV as per GAMP 5, 21 CFR Part 11 and EU Annex 11 for all GxP computerized systems.
Learn moreHPLC & Lab Instrument Validation
Qualification and software validation of HPLC, GC, UV and other QC laboratory instruments.
Learn morePLC Validation
Validation of PLC-based process equipment used in pharmaceutical manufacturing.
Learn moreHMI Validation
Validation of Human Machine Interfaces including security, recipes, alarms and audit trails.
Learn moreSCADA Validation
Validation of SCADA, BMS and EMS systems for complete plant-wide data integrity.
Learn moreExcel Spreadsheet Validation
Development and validation of GxP Excel spreadsheets for QC, QA and production calculations.
Learn moreHardware & Electronics Supply
Supply of industrial hardware, computers, networking and electronic components for pharma plants.
Learn moreCCTV Camera Installation
Supply, installation and maintenance of CCTV / IP camera systems for plants, warehouses, offices, shops and homes.
Learn moreCustom Software Development
New software development for pharma and other industries — web, desktop and mobile applications.
Learn moreGo Paperless with GxP-Ready Software
In-house developed products designed for pharmaceutical compliance, built and validated by the same team.
Pharma Pilot
An integrated pharma operations platform to digitize and manage day-to-day QA, QC and production activities.
- Centralised dashboard
- Workflow & approvals
- Role-based access
E-Logbook
Replace paper logbooks with secure electronic logbooks for equipment, instruments, areas and cleaning.
- Equipment usage & cleaning logs
- Electronic signatures
- Real-time review
E-BMR
Electronic Batch Manufacturing Record for paperless, error-free and faster batch release.
- Step-by-step batch execution
- Auto calculations & checks
- Deviation capture
HRMS
Complete Human Resource Management System — employees, attendance, leave, payroll and more.
- Employee master & documents
- Attendance & leave management
- Payroll processing
Training Module (LMS)
GMP training management with training needs, schedules, online assessments and certificates.
- Training need identification
- Online tests & evaluation
- Training records & certificates
Gate Management System
SmartGate — digital control of everything that enters or leaves your plant: visitors, materials, vehicles and employees.
- QR-based visitor registration & E-Gate Pass
- Department & gate approval workflow
- Gate IN / Department OUT / Gate OUT tracking
Our Satisfied Clients
Trusted by leading engineering, pharmaceutical, laboratory, food and technology companies for validation, hardware and software solutions.
Larsen & Toubro Ltd. (L&T)
Engineering & ConstructionPunagri Organics & Lifesciences Pvt. Ltd.
API & Pharma IntermediatesSDI Tech Pvt. Ltd.
Tradjac Pvt. Ltd.
Glassware Pvt. Ltd.
Laboratory GlasswareNPS GMP Integrity Solutions
GMP & ComplianceGreen Software Solutions
SoftwareCrescent Pharma Ltd.
PharmaceuticalsAdhore Pharma Pvt. Ltd.
PharmaceuticalsNavjeevan Food Pvt. Ltd.
Food ProcessingOne partner for validation, hardware & software
We understand both pharma regulations and technology. That means your systems are not only working — they are audit-ready.
About UsRegulatory Expertise
Documentation aligned to GAMP 5, 21 CFR Part 11, EU Annex 11 and data integrity guidelines.
Fast Turnaround
Ready templates and experienced engineers mean faster project completion.
Data Integrity First
Audit trails, access control and electronic signatures built into everything we deliver.
Reliable Support
On-site and remote support from a local team based in Khalapur, Raigad.
Simple, Structured Validation Lifecycle
Plan
Validation Plan, URS & system risk assessment.
Specify
FS / DS, configuration & traceability matrix.
Verify
IQ, OQ, PQ execution with objective evidence.
Report
Validation summary report & release for use.
Maintain
Change control & periodic review support.