Industries · Compliance pathways

Regulated industries we support

Six sector pathways aligned with the NQSC Compliance Pathway Hub. Each industry page explains the regulatory context, typical documentation needs, and which NQSC service pages apply to your situation.

  • 25+Years Experience
  • 500+Companies
  • 6 Industries
  • India · Export

How to use this hub

  • 1Choose the industry that matches your product and site type
  • 2Review regulatory context and linked NQSC services
  • 3Open the service page for documents, process, and FAQs
  • 4Request consultation if your scope spans more than one pathway
6 industriesIndia · ExportDevices · PharmaLabs · Food

Quick sector match

  • Device licensing or exportMedical Devices
  • Pharma manufacturing or COPPPharma & GMP
  • Controlled rooms or HVACCleanroom & Validation
  • QMS or audit maintenanceManagement Systems

Sector groupings

Three compliance focus areas

Industries are grouped by how teams usually plan submissions. Open a sector page for detail, or jump to Services for the full list of specialist pages.

India device and pharma licensing

Best for: manufacturers, importers, and pharma sites regulated in India.

  • Medical Devices: CDSCO Rules 2017, MD forms, Sugam
  • Pharma & GMP: Schedule M, WHO TRS, COPP via CDSCO
  • Test, loan, manufacturing, and import license planning

Key topics

  • CDSCO
  • MD forms
  • WHO-GMP
  • COPP

Facilities, labs, and food context

Best for: hospitals, labs, food businesses, and controlled environments.

  • Healthcare & Labs: NABH and NABL frameworks (scope on consultation)
  • Food & Safety: FSSAI licensing context (scope on consultation)
  • Cleanroom & Validation: ISO 14644 qualification

Key topics

  • NABH
  • NABL
  • FSSAI
  • ISO 14644

QMS, export, and maintenance

Best for: certification, EU/US market access, and post-approval upkeep.

  • Management Systems: ISO 13485 for device QMS
  • Medical Devices: CE marking and US FDA 510(k) support
  • Audit, CAPA, and technical file maintenance

Key topics

  • ISO 13485
  • EU MDR
  • 510(k)
  • CAPA

CLIENT TRUST

What Clients Say About

Feedback from CDSCO, ISO, documentation, validation and compliance support work across India and export markets.

Trusted by regulated manufacturers, importers and compliance teams

25+ years

Compliance experience

500+ clients

Companies served

190+ ISO

Certificates supported

400+ companies

Regulatory support

Want similar clarity for your license, certification or audit requirement?

FAQ

Questions about industries and pathways

Short answers on choosing a sector page, scope limits, and how industries link to services.

Industry pages describe your sector and link only to published NQSC service landings. Service pages carry the detailed document lists, process steps, and service-specific FAQs.

Healthcare and Food pages explain those frameworks. NQSC maps support to existing services such as cleanroom validation, ISO 13485 where device QMS applies, or audit readiness. Confirm filing scope on consultation before you rely on a pathway.

Start with Medical Devices. It links to CDSCO, ISO 13485, CE marking, FDA 510(k), and technical file services. Exporters often need more than one service page.

Yes. Find My Compliance Path on the homepage captures industry, stage, and need. Industry pages are useful when you already know your sector and want linked services in one view.

Content references published CDSCO, WHO, ISO, EU MDR, FDA, FSSAI, NABH, and NABL sources. Requirements change; NQSC helps interpret them for your product class and site.

Ready to discuss your industry pathway?

Tell us your sector, whether you are licensing, certifying, validating, or preparing for audit, and which markets you serve. NQSC will outline next steps.

Call NQSC at +91 98102 36683

Expert-led regulatory and certification support across India and export markets.