TRD Consulting - Innovative Toxicology

πŸ§ͺ GLP Implementation and Compliance Advisory

Good Laboratory Practice (GLP) Consulting by Dr. Ramesh Subramani

Ensure your laboratory meets global GLP standards with expert guidance from Dr. Ramesh Subramani, a highly experienced Regulatory Toxicologist . With over two decades of experience in regulatory toxicology, Dr. Subramani specializes in GLP implementation, audit readiness, and compliance advisory for contract research organizations (CROs).

Whether you’re establishing a GLP-compliant system from the ground up or preparing for regulatory inspections by agencies such as OECD, US FDA, EMA, MHRA, or ANVISA, Dr. Ramesh offers tailored consulting to meet your organizational needs and regulatory goals.

πŸ” Services Include:

βœ… Full GLP system setup and gap analysis

βœ… SOP preparation, data review, and documentation

βœ… Internal GLP audits and mock inspections

βœ… Study Director training and competency building

βœ… GLP compliance remediation for existing labs

βœ… Vendor qualification for GLP studies

βœ… Guidance on OECD Principles of GLP and regional variations

βœ… My Credentials?

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Certified DABT (Diplomate of the American Board of Toxicology) and UK/ ERT (European Registered Toxicologist)

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Former Senior Toxicologist at leading organizations: Eurofins, Dr. Reddy’s Lab and BSL Bioservice

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Deep experience with GLP-based toxicology studies

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Member of Regulatory Professional Society, British Toxicology Society, Royal Society of Biology, and Safety Pharmacology Society

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Global client support for GLP accreditation, audits, and compliance

🌍 Serving Clients Worldwide

Get in touch for a customised regulatory toxicology consulting plan tailored to your molecule and target market.

Call now

+49 89 38048726

E-Mail Address

ramesh@trdconsultings.com