About Us

Sri Ramakrishna’s
Renomate

Sri Ramakrishna’s Renomate is a professionally managed medical device manufacturing organization specializing in the development, manufacturing, and supply of Haemodialysis Solutions and related products. The company is committed to supporting renal care by delivering products that meet the highest standards of quality, safety, and regulatory compliance.

11k+Sq. Ft. Facility
GMPCertified
MDR2017 Compliant
Renomate Mission

Manufacturing Excellence & Quality Systems

Our manufacturing facility is strategically located at No. 2, H3, H3 Road, Virudhunagar, Tamil Nadu, with an operational area of approximately 11,000 square feet. The facility has been meticulously designed and constructed in accordance with Good Manufacturing Practices (GMP) and complies with the structural and operational requirements of the Central Drugs Standard Control Organization (CDSCO) and the Medical Device Rules (MDR), 2017.

Our operations are governed by a comprehensive Quality Management System (QMS) to ensure consistency, traceability, and continual improvement across all processes. Quality is not just a regulatory requirement—it is a core organizational value.

In-house Laboratory

Our Quality Control and Testing Laboratory is fully equipped for raw material testing, in-process control, and finished product analysis.

  • Atomic Absorption Spectroscopy (AAS)
  • Wet Chemistry Laboratory
  • Microbiology Laboratory

Raw Materials & Supplier Quality Assurance

At Sri Ramakrishna’s Renomate, the quality of raw materials is fundamental to the safety and performance of our haemodialysis solutions.

Premium Sourcing

Indian Pharma Grade raw materials from approved vendors and food-grade cane-based ingredients for high purity.

Stringent Testing

Incoming raw materials and finished goods undergo strict quality checks. Each batch is tested for identity, purity, and quality as per IP/BP specifications.

Traceability

Complete traceability and documentation are maintained in line with QMS and MDR 2017 requirements.

Regulatory Compliance

We strictly adhere to applicable national regulatory standards and guidelines, ensuring our systems support regulatory inspections and continuous compliance.

MDR 2017CDSCO RequirementsGMP CertifiedQMS Principles

Technical & Quality Leadership

Mr. M. Palanivelu

M.Pharm
Technical Head

Responsible for manufacturing operations, process validation, quality systems, and regulatory compliance.

Mr. S. Gurusamy

M.Sc (Chemistry)
Quality Control

Oversees analytical testing, laboratory operations, and compliance with quality standards.

Mrs. K. Saraswathy

B.Sc (Chemistry)
Quality Control

Supports routine analysis, documentation, and quality assurance activities.

Mr. B. Prakash

B.Tech
Medical Device Designer

Responsible for design inputs, technical documentation, product development support.

Mr. A. Saravanakumar

M.Sc (Microbiology)
QC - Microbiologist

Responsible for microbiological testing, sterility assurance, and environmental monitoring.

Management & Governance

Sri Ramakrishna’s Renomate is led by its partner firm:

  • Mr. B. Suresh
  • Mrs. R. Meenal

The leadership team is committed to ethical business practices, regulatory transparency, and long-term sustainability. Their vision emphasizes patient safety, customer satisfaction, and excellence in manufacturing.

Our Vision

To be a recognized and trusted manufacturer of haemodialysis solutions, delivering reliable, safe, and high-quality medical devices that contribute to improved renal care and patient well-being.

Our Mission

  • Manufacture solutions meeting highest quality/safety standards.
  • Operate in full compliance with CDSCO, MDR 2017, GMP, and QMS.
  • Continuously enhance quality through innovation and optimization.
  • Build long-term partnerships through trust and reliability.

Commitment to Patients & Healthcare

We understand the critical role haemodialysis solutions play in patient care. Therefore, every aspect of our manufacturing process—from raw material selection to final product release—is driven by a commitment to patient safety, clinical effectiveness, and regulatory excellence.