Centecura Healthcare offers specialized Healthcare Compliance Services in India, enabling pharmaceutical, biotechnology, and medical device companies to meet complex regulatory and ethical standards. With deep domain knowledge of Indian and international healthcare regulations, Centecura supports organizations in achieving full compliance with CDSCO, NABH, ICH-GCP, WHO-GMP, and global regulatory frameworks such as USFDA, EMA, and MHRA.
Our compliance solutions are designed to reduce risk, strengthen internal controls, and support seamless audits and inspections. We provide end-to-end assistance in policy development, SOP implementation, internal audits, mock inspections, risk assessments, and staff training to ensure quality, safety, and accountability across clinical, manufacturing, and operational functions.
Key offerings include:
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Regulatory Compliance Audits & Gap Assessments
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GxP (GLP, GMP, GCP) Compliance Support
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Clinical Trial Oversight & Documentation Review
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Data Integrity & Quality Management System (QMS) Implementation
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Standard Operating Procedures (SOPs) Design & Training
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Medical Device Regulatory Compliance (ISO 13485, MDR, etc.)
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Post-Market Surveillance & Pharmacovigilance Compliance
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Support for NABH Accreditation & Hospital Compliance
Centecura’s expert team ensures clients stay ahead of compliance updates and avoid costly delays or penalties. Whether you're launching a new facility, undergoing regulatory inspection, or strengthening your internal quality systems, we deliver practical, audit-ready solutions that align with evolving healthcare standards in India.
Partner with Centecura Healthcare – your trusted compliance ally to drive operational excellence and ensure sustained regulatory success.
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