Healthcare & Pharma Problem-Solving Lab — Global Edition
(Pharma, Biotechnology, Hospitals, Diagnostics, Medical Devices, HealthTech)
Clinical GRC + Hospital Compliance Systems
Live on Zoom + secure browser backup access.
June 17, 2026
Ticket
USD 49
Free for GC360 Members
USD 299/year
Unlimited access to all Labs, Masterclasses & Toolkits.
About This Industry Lab
A global, sector-specific Lab where legal, compliance, clinical governance, privacy, cyber, risk, quality assurance and regulatory teams learn how hospitals, clinical research environments and pharmaceutical organisations operationalise practical, audit-ready GRC systems across care delivery, data flows and regulated operations.
This is not a panel.
This is a challenge-solving room.
What You Will Solve (May Focus: Clinical GRC & Operational Compliance)
Learn how Healthcare & Pharma leaders build structured, regulator-ready compliance systems through:
Clinical workflows: approvals, treatment pathways, data access rules
Clinical trial GRC — study governance, PI compliance & sponsor audits
Hospital-level GRC systems for privacy, safety & documentation
Building audit-ready logs for EHR, LIS, PACS, IoT & medical devices
Patient data lifecycle: collection, storage, access, retention & deletion
Creating regulator-ready DPIAs, risk registers & compliance evidence
Vendor risk in hospitals, labs, clinical trial partners & CROs
Managing third-party systems: e-consent, telehealth, lab systems, CDM
Release-cycle governance for digital health apps & patient platforms
Handling regulatory overlaps: HIPAA, GDPR, DPDP, EMA, FDA, MHRA, HSA
Operationalising AI controls in diagnostics, labs, radiology & research
Preparing for sponsor audits, ISO reviews & national health authority checks
All content is example-driven, execution-focused, and usable immediately.
Unlimited access to all Labs, Masterclasses & Toolkits.
How This Global Lab Works (90-Minute Agenda)
Global Problem Framing (10 min)
A clear, sharp overview of today’s hospital, clinical and pharma governance challenges — documentation, audit preparedness, system controls and patient safety.
Expert Deep-Dive (40 min)
Global leaders share their:
-
Audit frameworks
-
Clinical GRC systems
-
Patient data controls
-
Medical device + IoT governance
-
Hospital compliance playbooks
-
Real examples from labs, trials & treatment environments
This is the core of the Lab.
Delegate Challenge Exchange (20 min)
Delegates share challenges, learnings and insights — supporting one another with practical, applied solutions.
Experts respond live with clear, immediate guidance.
Joint Problem-Solving (20 min)
Speakers and delegates solve real healthcare & pharma cases:
Clinical data access • Device logs • CRO/vender controls • AI diagnostics • Audit documentation gaps • Clinical risk scoring
Unlimited access to all Labs, Masterclasses & Toolkits.
Speaker Board (Global Healthcare & Pharma Leaders)
A curated panel of senior regulatory, quality, GRC, clinical governance, privacy and cyber leaders from global hospitals, pharmaceutical companies, lab networks and digital health organisations.
(Speakers to be announced soon)
Why Most Participants Upgrade to Membership (USD 299/year)
GC360 Members receive unlimited access to:
-
All Industry Labs (24/year)
-
100+ Privacy, AI, Cyber, GRC & Contract Toolkits
-
20+ Deep-Dive Masterclasses
-
GC360Flix — 200+ hours on-demand
-
Curated introductions with global peers
-
GC360 Talent Match & mentorship circles
-
Speaking opportunities at global events
Unlimited access to all Labs, Masterclasses & Toolkits.
Global Credibility
Previous speakers from: Pfizer • Mayo Clinic • Johnson & Johnson • NHS • GE Healthcare • Roche • Philips • UnitedHealth • Cerner • Takeda • Novartis • Siemens Healthineers • and more
Delegates from: APAC • MEA • UK/EU • USA • Canada • Australia • Africa
What Delegates Say
.jpg)
Sofia Sjöö
Mölnlycke Health Care (Sweden)
“A highly valuable session with diverse expert perspectives. Insightful and engaging.”
Renata Berzanskiene
Legal Counsel, UAB Vilniaus Degtine (Lithuania)
“The emphasis on attorneys personally verifying legal authorities was excellent. I’d also love to see deeper exploration of the EU AI Act.”
Alexander Wold
Monks (USA)
“As a cybersecurity professional, I found the legal and privacy insights invaluable—bridging perspectives that are often siloed.”
Unlimited access to all Labs, Masterclasses & Toolkits.
Partners
Global Thought Leadership Partner
Powered By
Digital Content Library Partner
