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!
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Clinical Evaluation for Medical Devices: CER Compliance & Regulatory Readiness
Master the art of clinical evaluation and CER readiness to ensure regulatory compliance, safety, and performance of medical devices under global frameworks.
₹100,000 -
PharmaConnect: Building Trust & Driving Sales
Master the art of ethical, impactful, and strategic selling in the pharma industry through real-world insights and simulations.
₹120,000 -
MDR Technical Documentation for Audit Readiness
Master the essentials of MDR-compliant technical documentation to accelerate approvals and withstand regulatory scrutiny.
₹100,000 -
PMS & Vigilance under MDR and IVDR
Strengthen compliance and patient safety through robust PMS and vigilance practices under MDR and IVDR.
₹120,000 -
Performance Evaluation & Clinical Evidence for IVDs
Driving compliance and market success through robust performance evaluation and clinical evidence for IVDs.
₹100,000 -
US FDA Regulations for Medical Devices
Master FDA regulatory pathways to bring safe and compliant medical devices to the US market
₹100,000 -
AI/ML Medical Devices: US & EU Regulatory Pathways
Master US FDA and EU MDR/IVDR pathways for regulatory compliance of AI/ML-enabled medical devices.
₹120,000 -
QMS Metrics & Data Integrity for Decision Making
Driving compliance and business excellence through QMS metrics and robust data integrity practices.
₹100,000 -
Import & Export Compliance in FMCG: Customs Rules & Best Practices
Ensuring compliance and efficiency in FMCG global trade through mastery of import/export regulations and customs rules.
₹100,000 -
Food Additives, Preservatives & Novel Foods: Regulatory Compliance Essentials
Navigating regulatory frameworks for food additives, preservatives, and novel foods to ensure compliance and market readiness.
₹100,000 -
Global Market Authorisation for SaMD & MDSW
Navigating global regulatory pathways to achieve safe, compliant market authorisation of SaMD and MDSW.
₹100,000 -
Pharmaceutical Distribution Compliance: Good Distribution Practice (GDP) Essentials
Safeguarding pharmaceutical integrity through compliant, risk-based Good Distribution Practices.
₹120,000 -
EU IVDR: Compliance & Market Access for In Vitro Diagnostics
Understanding EU IVDR requirements to ensure compliant, evidence-based market access for in vitro diagnostics.
₹100,000 -
EU MDR : Compliance & Market Readiness for Medical Devices
Building compliance readiness for the European Union Medical Device Regulation (MDR 2017/745).
₹90,000 -
Import & Distribution Compliance for Global Market Access
Strengthening compliance by defining and fulfilling importer and distributor obligations under EU MDR/IVDR and global frameworks.
₹100,000 -
Sustainability & ESG Integration into QMS
Integrating ESG imperatives into Quality Management Systems to drive compliance, resilience, and sustainable value creation.
₹90,000 -
Greening Automotive: ISO & Regulatory Practices
A deep-dive into environmental regulations, ISO standards, and sustainable operations reshaping the automotive industry.
₹120,000 -
US-FDA Audit Preparedness – Corporate Program
A tailored, organization-wide engagement designed around your company’s audit history and compliance challenges.
₹50,000 /Day Onwards