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MSR LogoCompliance Consulting

Healthcare Compliance, Clinical Safety & NABH/ISO Standards

Achieve NABH accreditation guidelines, implement ISO 13485 medical device standards, and secure bio-waste permits.

Pricing ModelGet Customized Quote
Processing Time10-15 days
Success Rate98%
Professional Advisory
Quote on Request
Govt. fees communicated separately & upfront
Processing Time10-15 days
Expert AssignedCS / Compliance Expert
CommunicationWhatsApp + Email
Process100% Digital
100% Compliance Guarantee — regulatory adherence at zero risk

About This Service

Healthcare organizations must maintain clinical quality standards to ensure patient safety, protect medical records, and comply with state medical regulations. Whether you operate a multi-specialty hospital, a diagnostic laboratory, or manufacture medical devices (ISO 13485), regulatory compliance is non-negotiable. MSR Assessment helps healthcare providers structure operational policies, optimize sterilisation protocols, maintain patient privacy logs, and align facilities with NABH and international QMS frameworks. MSR Assessment Pvt Ltd's experienced legal counsels and company secretaries manage the complete process on your behalf — ensuring all statutory documents and governance frameworks are legally sound. Our experts have handled hundreds similar cases and understand every nuance of this process.

Key Benefits

CS & Legal Specialist
Handled by certified company secretaries and legal governance counsels.
Legal Safety & NOCs
Protect healthcare facilities from negligence claims, license suspension, or local registry penalties.
TPA & Insurance Tie-ups
Qualify for direct TPA panels and cashless insurance payouts through certified status.

Eligibility Criteria

  • Hospitals & Nursing Homes
  • Diagnostic Labs & Imaging Centers
  • Medical Device Manufacturers
  • Dental & Eye Clinics
  • Pharmaceutical Distributors

Documents Required

Clinical Establishment License
Biomedical Waste Management Permit
Radiation Safety Certificate (AERB)
ISO 13485 QMS Manual (for device makers)
Staff Qualification & Hygiene Logs

Our expert will provide a precise document checklist specific to your case after your consultation.

Our Process

1
Clinical Gap Audit

Inspecting clinical labs, sterilization setups, and emergency procedures.

2
Protocol Structuring

Drafting patient safety manuals, pharmacy logs, and bio-waste treatment rules.

3
On-Site Staff Training

Training nurses, lab assistants, and technicians on compliance standards.

4
Accreditation Submission

Coordinating clinical reviews with registry officers to secure NABH or ISO certification.

Frequently Asked Questions

Biomedical waste management authorization is typically granted by State Pollution Control Boards for three (3) to five (5) years and must be renewed prior to expiry with audited disposal records.
ISO 13485 is a specialized Quality Management System standard for the medical devices sector. It ensures consistency in design, development, production, and installation of safe medical devices.

Why Work With MSR?

Stay compliant with corporate laws, MCA filings, and labor regulations under expert CS guidance.

Practicing Company Secretaries (CS)
Annual Compliance Calendars
Proactive Statutory Deadlines Tracking
Flawless MCA V3 Portal Filings
Corporate Governance Audits
Legal Risk Mitigation Advisory
Success!