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Hazardous & Chemical Waste Management

Hazardous waste classification, CPCB authorisations, manifest systems, and annual returns: for facilities generating the complex streams.

Overview

Pharmaceutical manufacturing produces spent solvents, distillation residues, spent catalysts, contaminated packaging, and biomedical waste: some of the most scrutinised waste streams in Indian industry. We handle classification under the HW Rules 2016, CPCB/TSPCB/APPCB storage and disposal authorisations, manifest system design, annual returns, and MSIHC Rules compliance. Dr. GSR has managed these streams at scale across API and formulation facilities.

Key Deliverables

  • Hazardous waste inventory and Schedule I/II/III classification
  • CPCB / TSPCB / APPCB authorisation for hazardous waste storage and disposal
  • Waste manifest system design and staff training
  • Annual returns under Hazardous Waste Management Rules
  • MSIHC Rules compliance audit and documentation
  • Biomedical waste management plan
  • EPR (Extended Producer Responsibility) registration support

Applicable Regulations

  • · Hazardous & Other Wastes (Management & Transboundary Movement) Rules, 2016
  • · MSIHC (Manufacture, Storage & Import of Hazardous Chemicals) Rules, 1989
  • · Biomedical Waste Management Rules, 2016
  • · Plastic Waste Management Rules (EPR), 2022
  • · CPCB / TSPCB / APPCB authorisation requirements

Why Dr. GSR

Three decades managing pharmaceutical hazardous waste across multiple Telangana facilities. API residues, solvent streams, spent catalysts. Clean enforcement record throughout.

Our Process

01

Assess

Understand your current situation: operations, regulatory standing, existing documentation, and compliance gaps.

02

Plan

Develop a tailored approach: scope, timelines, deliverables, and regulatory strategy specific to your industry and location.

03

Implement

Execute: whether that means preparing documents, conducting studies, liaising with authorities, or running training sessions.

04

Monitor

Establish monitoring programmes and review cycles to ensure compliance is maintained: not just achieved once.

Get in touch

Talk to Dr. GSR.

No intake forms. No junior consultants. You get direct access — describe the situation and we'll take it from there.