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!
Regulatory Requirements for Economic Operators – Importers & Distributors ObligationsGain deep insights into the regulatory responsibilities and compliance challenges of importers and distributors under…
₹85,000
FDA Regulations – Regional Nuances & Requirements for Medical DevicesNavigate FDA’s regulatory pathways, regional nuances, and compliance requirements for successful U.S. medical device market…
₹90,000
Global Food Safety Standards (ISO 22000, GFSI, BRCGS, etc.)Strengthen global food safety compliance and operational excellence by LISO 22000, GFSI, and BRCGS standards
₹95,000
Good Manufacturing Practices (GMP) in Food & Beverage – Compliance, Quality & Operational ExcellencePractical insights into Good Manufacturing Practices (GMP) for ensuring compliance, quality, and operational excellence in…
₹90,000
TGA Australia Regulations for Medical DevicesNavigate Australia’s TGA regulations, ARTG pathways, and compliance essentials for successful medical device market access.
₹90,000
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