ARK Pharmatech SolutionsARK PharmatechSolutions
Our Commitment

Quality & Compliance.

Each part is crafted with precision and undergoes strict quality checks to meet industry standards — delivering dimensional accuracy, surface finish, and consistency with timely delivery.

GMP-AwareIn-Process ControlsStrict Quality ChecksTimely Delivery
MATERIAL CERTS

On request

INSPECTION

In-process + final

QUALITY CHECKS

Industry standards

DELIVERY

Timely · to spec

High-accuracy parts from an in-house machine shop

Dimensional accuracy, superior surface finish, and consistency.

We manufacture high-accuracy components in ferrous, non-ferrous metals, and engineering plastics using advanced CNC and VMC machines. Whether a prototype, small-batch, or large-scale requirement — our team delivers the highest quality standards with timely delivery.

CNC TOLERANCE
±0.01mm

CNC milling and turning across in-house equipment

SURFACE FINISH
Ra 0.8μm

Achievable surface finish on machined components

GEOMETRY
5-axis

Rotary tables for complex 5-axis machining

MATERIAL RANGE
SS/Al/Plastics

Ferrous, non-ferrous metals, and engineering plastics

MANUFACTURING
GMP-aware

Processes designed to support GMP-compliant systems

DOCUMENTATION
FDA-aligned

Material certification and traceability records

QUALITY CONTROL
In-process

In-process and final inspection protocols

SUPPORT
Lifecycle

Engineering, AMC, and preventive maintenance

Equipment list

Key in-house equipment at our manufacturing facility.

  • HAAS (USA) VMC VF-2
  • HAAS (USA) VMC VF-5
  • Rotary tables for complex components
  • CNC Turning Centers
  • TIG-welded stainless fabrication cells
  • Calibrated measuring equipment
  • Tools, dies & molds workshop
  • Electronics & control panel assembly
01 / Philosophy
Quality philosophy

Quality is not an afterthought.

Quality is embedded across every aspect of our operations — from material selection to final delivery. Our systems are designed for regulated pharmaceutical environments where precision and compliance are essential.

We understand that in the pharmaceutical industry, quality is not just about meeting specifications — it's about ensuring patient safety and maintaining the integrity of your production processes.

Quality pillars

Process controlControlled workflows at every production stage
TraceabilityComplete documentation on request
RepeatabilityConsistent dimensional accuracy across runs
Material integrityQualified sourcing from certified suppliers
02 / Pillars
Our approach

Four pillars of quality.

Quality is embedded across four key areas of our operations, ensuring consistent, reliable outcomes for every component we manufacture.

Material Selection

Rigorous material qualification and sourcing from certified suppliers to ensure consistent quality and traceability.

Manufacturing Processes

Controlled manufacturing workflows with in-process quality checks at every critical stage.

Inspection & Validation

Comprehensive inspection protocols and validation procedures to ensure all products meet specifications.

Documentation & Traceability

Complete documentation packages with full traceability for regulatory compliance and audit readiness.

Strict quality checks to meet industry standards
Dimensional accuracy and surface finish
Consistent manufacturing across production runs
In-process quality controls
Final inspection protocols
Material certification on request
GMP-aware manufacturing processes
Timely delivery to specifications
03 / Compliance
Regulatory alignment

Designed for regulated environments.

While machining suppliers are not directly GMP-certified, our processes are designed to support GMP-compliant systems. We ensure consistent dimensional repeatability, controlled workflows, and traceability-ready documentation.

Our parts integrate seamlessly into pharmaceutical packaging and fill-finish systems, supporting your validated equipment performance.

04 / Standards
Standards & compliance

Manufacturing aligned to pharmaceutical standards.

Our engineering processes are designed around the quality requirements of regulated pharmaceutical manufacturing — supporting Schedule M, cGMP, and international standards.

Schedule M / cGMP

Equipment design and fabrication aligned to Schedule M requirements of the Drugs and Cosmetics Act (India) and cGMP principles for pharmaceutical manufacturing.

Material Traceability

All SS 316L and SS 304 materials are sourced with mill test certificates (MTC). Material traceability documents provided with every fabrication and machined component on request.

Dimensional Inspection

In-process and final dimensional inspection using calibrated instruments. Inspection reports available with critical components for IQ/OQ validation documentation support.

Surface Finish Verification

Surface roughness (Ra) measured with calibrated profilometers. Product-contact surfaces verified to Ra ≤0.4μm (mirror) or Ra ≤0.8μm (satin) as specified.

FAT Support

Factory Acceptance Testing (FAT) support available at our Ahmedabad facility. Test protocols, data sheets, and photographic documentation provided on request.

Documentation Package

Complete documentation for each project: engineering drawings, material certificates, inspection reports, weld maps, and surface finish records — ready for audit and validation.

Get in touch

Quality You Can Rely On

Partner with us for precision-manufactured components that meet the highest quality standards.

sales@arkpharmatech.com