Built around regulated operation.
Engineering and digital decisions developed with GMP, GAMP 5, data integrity and lifecycle requirements in mind.
PHARMACEUTICAL ENGINEERING · AUTOMATION · VALIDATION · COMPLIANCE
Better systems.
Stronger teams.
Inspection-ready operations.
Medicing helps pharmaceutical manufacturers design, automate, upgrade, validate and maintain GxP systems—from plant engineering and PLC/SCADA modernization to CSV, data integrity, training and regulatory inspection readiness.
700+ systems completed through Medicing engagements
ENGINEERING IN FOCUS
Engineering. Automation. Digital. Validation.
Medicing company experience
Practical delivery across pharmaceutical systems and regulated operations.
700+Systems completed through Medicing engagements
500+Days of audits & reviews
30Computerized system upgrades completed
ABOUT US / WHY Medicing
One partner across engineering, automation, validation and compliance.
Engineering. Automation. Digital. Validation. Compliance.
Medicing Automations & Technologies Pvt. Ltd. delivers integrated pharmaceutical solutions from concept to inspection readiness.
We bring technical implementation and regulatory evidence together so systems are built correctly, documented properly and ready for regulated operation.
One coordinated team.
Assessment, engineering, automation, software, validation, documentation, training and inspection readiness through one coordinated team.
The system comes first.
Experience across multiple equipment manufacturers, PLC platforms, SCADA systems and pharmaceutical processes.
From findings to action.
From identifying a gap through remediation, implementation, qualification and sustained compliant operation.
OUR CAPABILITIES
From your first blueprint
to your next inspection.
Integrated capabilities across the pharmaceutical system lifecycle.
01 / Medicing CAPABILITIESPlant Design & Project Management
Pharmaceutical facility planning, engineering coordination, project execution support, equipment planning and lifecycle management.
Discuss plant engineering02 / Medicing CAPABILITIESComputerized System Validation
Risk-based CSV for GxP computerized systems, including planning, requirements, risk assessment, qualification, traceability and lifecycle documentation.
Start with a GAP Assessment
03 / Medicing CAPABILITIESRegulatory Audit & Inspection Readiness
Structured readiness assessments, gap identification, remediation planning, evidence review and inspection preparation.
Explore inspection readiness04 / Medicing CAPABILITIESPLC, HMI & SCADA Modernization
Legacy automation modernization across Mitsubishi, Allen-Bradley, Siemens and Noxview platforms, including PLC, HMI, IPC and SCADA upgrades for regulated pharmaceutical operations.
Discuss a system upgrade
05 / Medicing CAPABILITIESPharma Software & Digital Solutions
Pharmaceutical applications, workflow automation, validation-ready software, databases, document systems and Pharma 4.0 solutions.
Discuss digital solutions06 / Medicing CAPABILITIESPharmaceutical Machine Engineering
Engineering support covering mechanical, electrical, instrumentation, automation, qualification and machine lifecycle requirements.
Discuss machine engineering
07 / Medicing CAPABILITIESTraining & Capability Development
Practical training for Engineering, QA, Validation, IT, Production and Automation teams covering regulated systems and inspection readiness.
Explore training programs
08 / Medicing CAPABILITIESData Integrity & Compliance
Access control, audit trails, electronic records, backup and restore, system security, ALCOA+ principles and data-integrity remediation.
Discuss data integrityAUTOMATION & LEGACY MODERNIZATION
Multi-platform automation expertise.
Built for regulated pharmaceutical operations.
Medicing supports automation projects and legacy-system modernization across Mitsubishi, Allen-Bradley, Siemens and Noxview hardware and software platforms.
PLC & control systems
Modular controllers, I/O and control-panel engineering.
Industrial PCs (IPC)
Industrial computing for dependable plant-floor operation.
HMI & SCADA
Operator interfaces and connected process supervision.
MITSUBISHI
PLC · HMI · Control Systems
ALLEN-BRADLEY
PLC · HMI · SCADA · Industrial Automation
SIEMENS
PLC · HMI · SCADA · Automation Systems
NOXVIEW
HMI · SCADA · Supervisory Systems
South India System Integrator
Medicing is the South India system integrator for Noxview Systems. Mitsubishi, Allen-Bradley and Siemens references describe project experience and do not imply manufacturer authorization, certification or endorsement.
Legacy System Upgrades for Pharmaceutical Manufacturing
Medicing has experience supporting OSD and injectable manufacturing systems, including HMI, IPC and PLC upgrades designed to address computerized-system, data-integrity and lifecycle requirements using GAMP 5-aligned principles.
Legacy Modernization
Upgrade obsolete PLC, HMI, IPC, SCADA and supporting hardware/software while considering operational continuity, lifecycle risk and validation impact.
GxP Automation
Modernization strategies can address user access, auditability, data integrity, backup and recovery, system security and controlled operation.
Validation Integration
Automation changes can be followed by risk assessment, qualification, CSV and documented evidence through Medicing’s integrated validation capability.
Modernize the technology. Preserve control. Validate the result.
A GAP Assessment identifies the deficiencies that guide remediation. Where modernization is needed, Medicing can integrate the upgrade with CSV/qualification, inspection readiness and lifecycle support.
HOW WE WORK
From Gap to
Sustained Compliance
Start with one system. Identify the gaps. Fix what matters. Validate the solution. Sustain compliance.
01
ASSESS
CSV GAP Assessment
Evaluate the current computerized system to identify validation, technical, data-integrity, procedural and lifecycle gaps.
View assessment scope
- Validation status
- user access
- audit trails
- backup and restore
- hardware/software status
- configuration
- documentation
- data integrity
- procedural controls
DELIVERY FOCUSStructured GAP Assessment Report with prioritized recommendations and next actions.
02
REMEDIATE & UPGRADE
GAP Remediation & System Upgradation
Implement only the remediation required based on identified gaps.
View typical activities
- Hardware replacement
- operating system or software upgrades
- PLC/HMI/SCADA modernization
- audit trails
- access control
- backup/restore
- database/server improvements
- configuration
- SOPs
- technical documentation
- data-integrity remediation
FINDINGS-LED SCOPEA remediation scope driven by actual findings. A major hardware or software upgrade is not required for every system.
03
VALIDATE
Computer System Validation / Qualification
Generate documented evidence that the remediated or upgraded computerized system is fit for intended use and appropriate for regulated operation.
View typical activities
- GxP assessment
- validation planning
- user requirements
- risk assessment
- design/specification review
- IQ
- OQ
- PQ where applicable
- traceability
- deviation management
- validation report
- lifecycle documentation
DELIVERY FOCUSDocumented evidence and a traceable validation package for the agreed system scope.
04
PREPARE
Compliance Review & Audit / Inspection Readiness
Review the system, documentation and operating controls to identify remaining readiness risks before regulatory or customer inspection.
View typical activities
- Validation evidence
- user access
- audit trails
- backup/restore
- change control
- SOPs
- training evidence
- deviations
- CAPA
- system operation
- data integrity
- interview preparation
DELIVERY FOCUSA prioritized readiness review. This phase may begin during the later stages of validation where appropriate.
05
SUSTAIN
Lifecycle Compliance Support
Maintain the validated state and support continued inspection readiness throughout the system lifecycle.
View typical activities
- Periodic review
- annual system health checks
- access review
- audit trail review
- backup/restore verification
- change-control assessment
- validation maintenance
- requalification
- ongoing readiness review
- lifecycle documentation
DELIVERY FOCUSAn agreed lifecycle support plan to maintain controls and respond to change.
Supporting capabilities
Engineering · Automation · Software · Data Integrity · Documentation · Training
Available across the engagement, according to your requirements.START WITH ONE SYSTEM
Not sure where your computerized system stands?
Start with a CSV GAP Assessment.
Identify potential gaps before they become larger validation, data-integrity or inspection-readiness issues.
Receive a structured gap report with recommended remediation priorities and next actions.
A clear starting point.
- Validation status
- User access & privileges
- Audit trails
- Backup & restore
- Hardware/software configuration
- CSV documentation
Starting from ₹5,000 / system
Final scope and applicable charges are confirmed before the assessment.
Request a GAP Assessment View Assessment ScopeSELECTED PROJECT EXPERIENCE
Engineering work.
Documented outcomes.
Selected Medicing engagement summaries across validation, automation and inspection readiness.
Computerized System Validation & Data Integrity
- Challenge
- An existing GxP computerized system required structured evaluation and remediation.
- Medicing scope
- Gap assessment, risk assessment, remediation support, qualification and lifecycle documentation.
- Outcome
- A structured validation package and improved system control for regulated operation.
Automation Modernization
- Challenge
- Legacy PLC/SCADA technology required modernization while maintaining pharmaceutical compliance.
- Medicing scope
- Engineering assessment, automation upgrade, testing, documentation and validation support.
- Outcome
- Modernized control architecture with improved lifecycle support and compliance readiness.
Regulatory Inspection Readiness
- Challenge
- A pharmaceutical operation required structured preparation for an upcoming inspection.
- Medicing scope
- Readiness assessment, evidence review, remediation planning, team preparation and follow-up assessment.
- Outcome
- A prioritized inspection-readiness program with identified risks and documented actions.
Project scope is engagement-specific. Inspection decisions remain with the relevant authority.
REGULATORY & TECHNICAL EXPERTISE
Compliance frameworks
we work with.
Technical decisions informed by the requirements of regulated pharmaceutical operations.
- GAMP 5
- 21 CFR Part 11
- EU Annex 11
- Data Integrity / ALCOA+
- GMP Qualification
- Risk-Based Validation
- Computer Software Assurance principles
- US FDA inspection readiness
- EU GMP inspection readiness
- WHO GMP readiness
These references describe areas of work. They do not imply regulator approval, certification or endorsement of Medicing.
Medicing CLIENT / PROJECT EXPERIENCE
Relationships across
the pharma ecosystem.
Pharmaceutical manufacturers, laboratories and engineering organizations.
- APL Healthcare Limited
- Adaarsh Pharmacon Industries PVT LTD.
- Alidac Healthcare (Myanmar) Ltd
- Amneal Oncology Private Limited
- Aurobindo pharma limited
- Axygen Pharmatech
- Basis Laboratories Private Limited
- Biological E. Limited
- Energon Labs Private Limited
- Evertogen Life Sciences Ltd.
- Fusion Scientific Laboratories Pvt. Ltd.
- Intas Pharmaceuticals
- Itaan pharma pvt ltd
- Megsan Labs private Limited
- NATCO Pharma Limited
- Nutron System Pvt Ltd
- Obvez Lab's Pvt Ltd.
- Optimus Pharma Private Limited
- Qdot Associates
- RCRI Private Limited
- Schematic Engineering Industries Pvt. Ltd.
- Teadus pharma Pvt Ltd.
- Topiox Research Centre Pvt. Ltd
TRAINING & CAPABILITY DEVELOPMENT
Build capability.
Bring it to the floor.
Professional training for Engineering, QA, Validation, IT, Production and Automation teams. Available independently or alongside your project.
Validation fundamentals
- CSV
- GAMP 5
- Risk Assessment
- Qualification
- Traceability
- Validation lifecycle
Automation & operations
- PLC
- HMI
- SCADA
- Alarm management
- System operation
- Change control
Data integrity & readiness
- ALCOA+
- Audit trails
- User access
- Backup & restore
- Electronic records
- Data review
Inspection preparation
- Interview readiness
- Evidence preparation
- Department coordination
- Observation prevention
- Remediation planning
Your team. Your systems. Your learning objectives.
Agree the syllabus, delivery format and schedule with Medicing.
FOUNDER & TECHNICAL LEADERSHIP
Gorthi
Sudarsana Rao
Founder & Managing Director
Medicing Automations & Technologies Pvt. Ltd.
1,000+
Pharmaceutical systems personally qualified during his professional career.
Founder’s personal professional experienceTechnical leadership.
A lifecycle perspective.
Gorthi Sudarsana Rao is a pharmaceutical engineering, computerized system validation and automation professional with more than two decades of experience in regulated pharmaceutical environments.
His expertise spans Computer System Validation (CSV), equipment qualification, PLC/HMI/SCADA systems, data integrity, risk-based validation, pharmaceutical engineering, lifecycle management and regulatory inspection readiness.
View Founder Profile
During his professional career, he has personally qualified more than 1,000 pharmaceutical systems across manufacturing, laboratory, utility and computerized system environments.
His professional experience includes responsibilities with leading pharmaceutical organizations including Dr. Reddy’s Laboratories, Biocon and Shilpa Medicare, together with international pharmaceutical assignments.
As Founder & Managing Director of Medicing, he leads the integration of engineering, automation, digital technology, validation and regulatory compliance into practical solutions for pharmaceutical manufacturers.
The organizations above relate to the founder’s previous professional experience and are not presented as Medicing clients.
PEOPLE & CAPABILITIES
Medicing Technical Team
Coordinated technical disciplines supporting delivery from initial assessment through lifecycle management.
- Validation & Qualification
- Automation Engineering
- Software Development
- Electrical & Instrumentation
- Documentation
- Project Management
- Regulatory Readiness
COMMON QUESTIONS
A clearer starting point.
Understand the scope, the sequence and the support available.
Start with a GAP AssessmentWhat services does Medicing provide to pharmaceutical manufacturers?
Medicing integrates pharmaceutical engineering, automation, digital solutions, computerized system validation, data integrity, training and inspection-readiness support.
What is a CSV GAP Assessment?
It is a structured review of a computerized system’s validation status, technical configuration, data integrity, documentation and operating controls. The output is a gap report with prioritized recommendations and next actions.
What happens after Medicing identifies gaps?
We discuss the findings with your team, prioritize risks and agree the remediation scope. The engagement can then progress through remediation, validation, readiness review and lifecycle support.
Does every GAP Assessment result in a hardware or software upgrade?
No. Remediation is based on actual system gaps. Some systems may require technical upgrades, while others may require configuration, procedural, documentation, access-control, data-integrity or validation remediation.
Can Medicing perform the remediation identified during the GAP Assessment?
Yes. Medicing can support technical, automation, software, documentation and procedural remediation within an agreed scope based on the assessment findings.
Can Medicing validate the upgraded or remediated system?
Yes. Medicing supports risk-based validation and qualification, including planning, requirements, testing, traceability, deviation management and lifecycle documentation.
Does Medicing support audit and regulatory inspection preparation?
Yes. Services include readiness assessments, evidence review, remediation planning, team preparation and follow-up review. Inspection outcomes are determined by the relevant authority.
Can Medicing maintain the validated state after qualification?
Medicing provides lifecycle support such as periodic reviews, access and audit trail reviews, backup/restore verification, change-control assessment and validation maintenance.
Can Medicing modernize legacy PLC, HMI and SCADA systems?
Yes. Medicing assesses existing control systems and supports modernization, integration, testing, documentation and validation according to the agreed requirements.
Does Medicing provide pharmaceutical software solutions?
Yes. Services include pharmaceutical applications, workflow automation, databases, document systems and digital solutions developed around regulated operational needs.
Does Medicing provide technical and corporate training?
Yes. Training covers validation, automation, data integrity and inspection preparation. Programs can be arranged independently or tailored to support a project.
Can Medicing support both new projects and legacy systems?
Yes. Medicing supports facility and system planning for new projects as well as assessment, remediation, modernization and lifecycle support for existing systems.
LET’S BUILD YOUR NEXT STEP
Your next project
starts with a conversation.
Talk with our engineering, automation, validation and compliance team about your next pharmaceutical project.
Book a Technical Consultation ↗Get in touch
Prefer to contact us directly?
CALL OUR TEAM+91 91771 68899EMAIL YOUR ENQUIRYsales@medicingenterprises.comFor project enquiries, service discussions and training requirements.