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!
Basic Biocompatibility: ISO 10993, Risk-Based Approaches & EU MDR EssentialsMaster ISO 10993 biocompatibility standards, risk-based approaches, and EU MDR essentials for medical device compliance
Free
Supplier Quality & Global Supply Chain ComplianceEquip leaders to strengthen supplier quality and ensure compliance in an increasingly complex global supply…
₹85,000
Emission Type Approval & BS-VI Compliance for Light Duty VehiclesNavigating emission compliance with confidence — from Type Approval to BS-VI readiness
₹95,000
Emission Type Approval & BS-VI Compliance for 2-WheelerMaster the complexities of BS-VI emission type approval and certification for 2-wheelers with real-world insights…
₹160,000
Clinical Evaluation for Medical Devices: CER Compliance & Regulatory ReadinessMaster the art of clinical evaluation and CER readiness to ensure regulatory compliance, safety, and…
₹100,000
PharmaConnect: Building Trust & Driving SalesMaster the art of ethical, impactful, and strategic selling in the pharma industry through real-world…
₹120,000
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