Huksa
Offered by Huksa, this L&D program is led by elite industry veterans—CXOs and Functional Heads with 25+ years of deep-domain expertise. You have the flexibility to customize the curriculum, select your preferred expert, and align the program to your organization’s specific objectives. Connect with the Huksa team to explore our array of top-tier trainers available for this course!
MDR Technical Documentation for Audit ReadinessMaster the essentials of MDR-compliant technical documentation to accelerate approvals and withstand regulatory scrutiny.
₹100,000
PMS & Vigilance under MDR and IVDRStrengthen compliance and patient safety through robust PMS and vigilance practices under MDR and IVDR.
₹120,000
Performance Evaluation & Clinical Evidence for IVDsDriving compliance and market success through robust performance evaluation and clinical evidence for IVDs.
₹100,000
US FDA Regulations for Medical DevicesMaster FDA regulatory pathways to bring safe and compliant medical devices to the US market
₹100,000
AI/ML Medical Devices: US & EU Regulatory PathwaysMaster US FDA and EU MDR/IVDR pathways for regulatory compliance of AI/ML-enabled medical devices.
₹120,000
QMS Metrics & Data Integrity for Decision MakingDriving compliance and business excellence through QMS metrics and robust data integrity practices.
₹100,000
Import & Export Compliance in FMCG: Customs Rules & Best PracticesEnsuring compliance and efficiency in FMCG global trade through mastery of import/export regulations and customs…
₹100,000
Food Additives, Preservatives & Novel Foods: Regulatory Compliance EssentialsNavigating regulatory frameworks for food additives, preservatives, and novel foods to ensure compliance and market…
₹100,000
Global Market Authorisation for SaMD & MDSWNavigating global regulatory pathways to achieve safe, compliant market authorisation of SaMD and MDSW.
₹100,000
Pharmaceutical Distribution Compliance: Good Distribution Practice (GDP) EssentialsSafeguarding pharmaceutical integrity through compliant, risk-based Good Distribution Practices.
₹120,000
EU IVDR: Compliance & Market Access for In Vitro DiagnosticsUnderstanding EU IVDR requirements to ensure compliant, evidence-based market access for in vitro diagnostics.
₹100,000
EU MDR : Compliance & Market Readiness for Medical DevicesBuilding compliance readiness for the European Union Medical Device Regulation (MDR 2017/745).
₹90,000
Import & Distribution Compliance for Global Market AccessStrengthening compliance by defining and fulfilling importer and distributor obligations under EU MDR/IVDR and global…
₹100,000
Sustainability & ESG Integration into QMSIntegrating ESG imperatives into Quality Management Systems to drive compliance, resilience, and sustainable value creation.
₹90,000
Greening Automotive: ISO & Regulatory PracticesA deep-dive into environmental regulations, ISO standards, and sustainable operations reshaping the automotive industry.
₹120,000
US-FDA Audit Preparedness – Corporate ProgramA tailored, organization-wide engagement designed around your company’s audit history and compliance challenges.
₹50,000 /Day Onwards
US-FDA Audit Preparedness – Deep Dive WorkshopA focused, simulation-driven workshop for QA/QC/RA managers to gain hands-on FDA audit readiness skills in…
₹8,490 /Seat
Agentic AI: Building Autonomous AgentsBuild, customize, and deploy next-gen AI agents using frameworks like LangGraph, CrewAI, Agno, and SmolAgents.
₹350,000