Pharmaceutical & Chemical Industries
Every batch must be reproducible, every action auditable, and every system validated.
Validated automation for the most demanding regulators on earth.
GMP-grade automation for pharmaceutical, biotech, and chemical manufacturing — 21 CFR Part 11, GAMP 5, and EU MDR compliant from day one. Reactor automation, batch control, utilities, and validated CIP/SIP systems delivered with the documentation regulators expect.
Where compliance, data integrity, and consistency are non-negotiable
Pharmaceutical and chemical operations face the most demanding regulatory environment in industry. Every batch must be reproducible, every action auditable, and every system validated. The cost of getting it wrong is measured in product recalls, regulatory observations, and lost market access.
Our pharma and chemical practice combines deep process knowledge with the validation discipline regulators expect. We deliver reactor automation, batch and continuous process control, utility systems, CIP/SIP, and the supporting electronic records and audit trails that turn an audit into a routine event rather than a crisis.
Across the pharmaceutical and chemical value chain
Reactor Automation
Jacket temperature control, pressure regulation, dosing automation, agitation profiles,
batch sequencing per ISA-88.
Fermentation
Bioreactor control for APIs, biologics, and specialty fermentation. DO, pH, temperature, and
feed control with substrate optimization
Pharma Water Systems
Purified Water (PW), Water for Injection (WFI), Pure Steam — generation, storage, hot-loop
distribution above 80°C.
Pharma Water Systems
Purified Water (PW), Water for Injection (WFI), Pure Steam — generation, storage, hot-loop
distribution above 80°C.
Distillation & Separation
Continuous and batch distillation with advanced control, solvent recovery, and energy optimization
CIP / SIP
Clean-In-Place and Sterilize-In-Place automation with cycle validation, conductivity
verification, and electronic batch records.
Batch Management
ISA-88 recipe management, equipment modelling, electronic batch records, exception handling and review-by-exception workflows.
Safety Shutdown Systems
ESD, F&G, and process safety per IEC 61511. Hazard analysis, SIL determination, and full safety lifecycle documentation.
Utility Systems
HVAC, compressed air, chilled water, nitrogen, vacuum — integrated control with energy
monitoring and contamination protection.
Audit-ready compliance frameworks
We combine decades of expertise with innovation, safety, and precision to deliver results that last.
21 CFR Part 11
FDA electronic records and signatures
EU Annex 11
European equivalent for computerized systems
ISA-88
Batch control and recipe management
EU MDR / FDA
For combination products and medical devices
ICH Q7, Q9, Q10
Pharmaceutical quality management
ISA-95
Enterprise-to-control system integration
IEC 61511
Functional safety for process industries
GAMP 5
Risk-based validation lifecycle
Validation discipline that turns audits into routine events
GAMP 5 Native
Risk-based validation built into every stage — not a documentation exercise at the end.
FDA & EMA Audit Track Record
Customer plants we have automated have passed multiple FDA and EMA inspections without observations on our systems.
ISA-88 Batch Expertise
Proper recipe modelling, equipment hierarchy, and exception management — not procedural code dressed up
Multi-Platform Validated
PCS 7, PlantPAx, DeltaV, Centum, 800xA — we deliver validated systems on every major DCS platform.
Pharma 4.0 Ready
Paperless batch records, MES integration, and continuous manufacturing approaches when you are ready.
Brownfield Discipline
We modernize legacy systems with phased validation that keeps existing licenses intact.
Why Choose VALORPLUS
Got questions about our engineering process or project delivery? Discover how we make engineering simple and effective.
What makes VALORPLUS different from other automation vendors?
VALORPLUS operates as an engineering partner, not just a vendor. We bring controls, electrical, and mechanical engineering under one team, ensuring fewer integration issues, faster delivery, and a single point of accountability from design to commissioning.
Do you work with specific automation platforms or multiple systems?
We are platform-agnostic. Our engineers work across Siemens, Rockwell, Mitsubishi, Schneider, Beckhoff, and other major ecosystems. This means we adapt to your existing setup — no forced migrations or vendor lock-in.
How do you ensure long-term maintainability of your solutions?
We follow a documentation-first approach. Every project is delivered with structured code, schematics, and manuals that your team can understand and maintain independently — reducing long-term dependency on external vendors.
Can you support projects outside India?
Yes. VALORPLUS is structured for global delivery, serving clients across India, Europe, the USA, and the Gulf. We align with regional standards such as IEC, NEC, and UL to ensure compliance in every market.
Do you provide end-to-end project support or only design services?
We support the full lifecycle — from concept and design to installation, commissioning, and post-go-live support. Our engineers stay involved until your system is fully operational and stable.
How do you ensure quality and reliability in automation projects?
We follow international engineering standards, structured programming practices, and a disciplined delivery process (Discover → Define → Design → Deliver → Support). Every solution is tested, documented, and validated before handover.
Can VALORPLUS work as an extended engineering team?
Yes. We offer flexible engagement models, including project-based delivery and embedded engineering support (T&M), allowing you to scale your team without long-term hiring commitments.
Do you use modern technologies like AI in engineering?
Yes. We use AI-assisted engineering workflows for mechanical and electrical design optimization, helping reduce design time, improve efficiency, and lower overall project costs — while maintaining full engineering accountability.
