Dr. Chandranand P.S.
Quality and Regulatory Advocacy with over three decades of experience in QC, QA, Regulatory Intelligence and Medtech & Biologics.
Delhi, India
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1. Director - IQzyme Medtech Pvt Ltd.
2. Member - Anusandhan National Research Foundation (ANRF), "MAHA MedTech Mission" Task Force Committee.
3. Global Consultant - WHO-Prequalification.
WHO PQ and regulatory intelligence advocacy and mentorship with extensive experience in regulatory testing of biologics, in vitro diagnostics (IVDs), and medtech innovation across public health laboratories, incubators, and national reference laboratories. Proven track record in strengthening local manufacturing, technology transfer, and quality systems for diagnostics and biotechnology derived therapeutics, including COVID-19 diagnostics and emergency response, process automations, LIMS, QMS, EQAAS etc. Adept at guiding startups, manufacturers, and government agencies on WHO Prequalification, Emergency Use Listing (EUL), accreditation, and regulatory testing, while building multi stakeholder partnerships to accelerate access to affordable, quality health technologies.
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(D1S1) Session 1: Quality Leadership — Building Inspection-Ready, Scalable Compliance
9:45 – 11:15 AM Session 1: Quality Leadership — Building Inspection-Ready, Scalable Compliance Session Chair: Manoj A, Independent Consultant, Former VP & Director – Global Product Development and Engineering, Terumo Penpol Pvt Ltd.
Session Focus: How to move from “audit preparation” to quality as a leadership system. Focus on ISO 13485 alignment, CAPA discipline, supplier controls, data integrity, design controls, and creating a culture where quality accelerates speed-to-market instead of slowing it down.
9:45 – 10:00 AM S1.T1: Redefining Quality: FDA’s Alignment with ISO 13485 and Its Impact on Manufacturers [15 min]
Rupam Chaudhury, Global Business Head, Medical, Lifesciences and Healthcare, L&T Technology Services (LTTS)
10:00 – 10:15 AM S1.T2: Beyond Compliance – Quality as a Leadership System [15 min]
Sreejith Viswam, Director – Innovation Enablers (RAQA, R&D Test Lab and R&D Operations), Stryker Global Technology Center, India
10:15 – 11:15 AM S1.T3: Panel Discussion [60 min] Moderator: Manoj A, Independent Consultant
Panelists: Speakers with the additional presence of:
3. Sarada Jayakrishnan, General Manager – Quality, Terumo Penpol Pvt Ltd
4. P.S. Chandranand, PhD, WHO Prequalification Consultant; Director, Iqzyme Medtech Pvt. Ltd
5. Srihariraju Manthena, Service Delivery Manager – BSI India Regulatory Services
Dr. Chandranand P.S.
Quality and Regulatory Advocacy with over three decades of experience in QC, QA, Regulatory Intelligence and Medtech & Biologics.
Delhi, India
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