Industry playbook
Hospitals & Healthcare
Every healthcare facility that generates bio-medical waste, from a 500-bed hospital to a dental clinic or diagnostic lab, needs authorization under the Bio-Medical Waste Management Rules and, in most states, consent from the pollution board. We handle authorization, consent, barcoding and tracking compliance, and the annual report due every June.
Where it goes wrong
The compliance risks we see most in this sector
- Getting a combined consent and bio-medical waste authorization for new or expanding facilities before the licence inspection.
- Segregating, barcoding and documenting waste handed to the common treatment facility as the rules require.
- Filing the Form IV annual report by 30 June with figures that reconcile with CBWTF manifests.
- Managing liquid effluent, radiology chemicals, and expired medicines under overlapping rules.
- Keeping fire NOC and consent renewals aligned so neither lapses during an accreditation cycle.
Your approvals
Services most relevant to you
In the order they are usually needed.
Waste Authorizations
Bio-Medical Waste Authorization
Every healthcare facility that generates bio-medical waste — from a multi-speciality hospital to a single-doctor clinic, dental practice, pathology lab or veterinary hospital — must obtain authorisation from the SPCB in Form III, segregate waste into colour-coded categories and submit a Form IV annual report by 30 June. We handle the application, the CBWTF agreement and the systems that keep you compliant.
- Starting price
- From ₹18,000
- Turnaround
- 15–60 working days
Pollution Control
Consent to Operate (CTO)
Consent to Operate is the SPCB's permission to run your plant, discharge treated effluent and emit through approved stacks. It also fixes the production capacity, fuel, water use and monitoring conditions you will be held to. We prepare the application, get your monitoring done by recognised labs and manage the inspection so production starts on schedule.
- Starting price
- From ₹20,000
- Turnaround
- 30–90 working days
Pollution Control
Consent Renewal (CTO Renewal)
A Consent to Operate must be renewed before it expires, and most SPCBs expect the application 60 to 120 days in advance with a full compliance record. We track your expiry dates, compile monitoring data and statutory returns, and file the renewal so your plant never operates on a lapsed consent.
- Starting price
- From ₹25,000
- Turnaround
- 20–60 working days
Pollution Control
Fire NOC (Fire Safety Certificate)
The Fire NOC, issued by the State Fire and Emergency Services Department, certifies that your building or factory meets the fire prevention and life safety norms of the National Building Code and the state Fire Act. A provisional NOC is needed at the building-plan stage and a final NOC before occupation or operation. We coordinate the fire-fighting layout, documentation and inspection so your project, factory licence and insurance are not held up.
- Starting price
- From ₹20,000
- Turnaround
- 15–45 working days
Waste Authorizations
Hazardous Waste Authorization
Any occupier who generates, stores, transports, uses or disposes of hazardous waste listed in the Hazardous and Other Wastes Rules needs an authorisation from the State Pollution Control Board in Form 2, valid for five years. We prepare the Form 1 application, set up your storage area, manifests and Form 3 register, and file the Form 4 annual return every 30 June.
- Starting price
- From ₹35,000
- Turnaround
- 30–120 working days
Audits & Advisory
Environmental Audit & Form V Statement
An environmental audit checks how your plant actually performs against its consent conditions, the Environment (Protection) Rules and the waste rules — pollution loads, monitoring, record-keeping, waste manifests and statutory returns. We audit the site, benchmark against the law and your consents, and produce a prioritised action plan plus the annual Environmental Statement in Form V that every consented unit must file by 30 September.
- Starting price
- From ₹60,000
- Turnaround
- 15–30 working days
ISO Certifications
ISO 9001:2015 Quality Management System (QMS) Certification
ISO 9001:2015 is the international standard for quality management and the certification most frequently asked for in vendor registration, government and PSU tenders and customer audits. It requires an organisation to understand its customers and context, control its processes, manage risk, measure performance and improve. We implement it in a way that fits your size, because a 20-person workshop should not end up with a 200-page manual, and take you through to an accredited certificate.
- Starting price
- From ₹20,000
- Turnaround
- 25–55 working days
ISO Certifications
ISO 13485:2016 Medical Devices Quality Management System Certification
ISO 13485:2016 is the quality management standard specific to medical devices, covering design and development, risk management (ISO 14971), traceability, sterile and clean-room controls, post-market surveillance and regulatory reporting. In India the Medical Devices Rules, 2017 require manufacturers to operate a quality management system conforming to the Fifth Schedule, which is closely aligned with ISO 13485, and CDSCO licence applications and notified-body audits expect it. It is also the gateway to CE marking, US FDA alignment and most export markets.
- Starting price
- From ₹45,000
- Turnaround
- 60–110 working days